Open Access

The zinc matrix metalloproteinase ZMP-2 increases survival of Caenorhabditis elegans through interference with lipoprotein absorption

  • Malaika Fischer1,
  • Elena Fitzenberger1,
  • Rebecca Kull1,
  • Michael Boll1 and
  • Uwe Wenzel1Email author
Genes & NutritionStudying the relationship between genetics and nutrition in the improvement of human health20149:414

https://doi.org/10.1007/s12263-014-0414-6

Received: 11 April 2014

Accepted: 17 June 2014

Published: 24 June 2014

Abstract

Matrix metalloproteinases are zinc-dependent endopeptidases conserved throughout the animal kingdom which primarily degrade components of the extracellular matrix. In the nematode Caenorhabditis elegans, the zinc matrix metalloproteinase (ZMP-2) was demonstrated to increase resistance versus heat and bacterial pathogens. Here, we show that the survival reducing activities caused by the knockdown of zmp-2 in C. elegans essentially requires the presence of vitellogenin-6, a protein homologous to mammalian apolipoprotein B, and RME-2, a receptor mediating endocytosis of cholesterol particles. Measurements of reactive oxygen species inside and outside C. elegans revealed that knockdown of zmp-2 causes a prooxidative extracellular mileu which is a prerequisite for the reduction of survival. Interestingly, RNAi for the foxo transcription factor daf-16 completely prevented those survival reducing effects of zmp-2 RNAi, and RNAi in mutants of the steroid signalling pathway revealed that DAF-16 acts by inhibition of DAF-9 and DAF-12. In conclusion, our study demonstrates survival reducing activities caused by the functional loss of ZMP-2 in C. elegans. Those effects are mediated by the transport of oxidized cholesterol adducts which then trigger the inhibition of DAF-9 and DAF-12 through the activation of DAF-16.

Keywords

Zinc matrix metalloproteinaseStress resistanceSteroid signallingFoxo transcription factorCholesterol absorptionApolipoprotein B

Introduction

In vertebrates matrix metalloproteinases represent a class of over 26 zinc-dependent enzymes which share a similar structure to each other and are capable of degrading almost every component of the extracellular matrix (Page-McCaw et al. 2007; Hernández-Pérez and Mahalingam 2012; Vu and Werb 2000). Those zinc matrix metalloproteinases are essentially involved in remodelling of the extracellular matrix in both physiological and pathological processes (Siefert and Sarkar 2012). As an example, matrix metalloproteinases (MMPs) are crucial for the generation or regeneration of arteries but their dysregulated activities may also be implicated in the pathogenesis of vascular diseases such as atherosclerosis (Siefert and Sarkar 2012). Interestingly, studies have shown that oxidized low-density lipoproteins and their receptor mediate the up-regulation of vascular factors associated with progression of atherosclerosis, such as MMP-9 (Lund et al. 2011). However, by the progressive accumulation and aggregation of LDL particles in the extracellular matrix, they become targets for oxidative but also enzymatic modifications (Badimon et al. 2011). It is interesting to note in this context that in mammalian keratinocytes, reactive oxygen species (ROS) mediate the effects of heat on tissue destruction and that the expression of several MMPs was induced contributing to tissue regeneration (Shin et al. 2008). Overall this suggests that complex interactions between LDL particles, redox metabolism and MMPs exist.

The nematode Caenorhabditis elegans has been described as an appropriate model to investigate the pathways of lipid storage, transport and signalling (Branicky et al. 2010). In the nematode homologues of apolipoprotein B are expressed in terms of vitellogenins (VITs), a class of egg yolk proteins in invertebrates but also in egg-laying vertebrates (Baker 1988). Since C. elegans is auxotroph for sterols (Chitwood and Lusby 1991), one important function of VITs is the provision of sterols to the organism (Matyash et al. 2001). Accordingly, cholesterol must be absorbed from ingested food in the intestine and later into the oocytes. Besides the VITs, transport at both loci requires the accomplishment of receptor-mediated endocytosis through RME-2 (Matyash et al. 2001; Grant and Hirsh 1999). RME-2 is a member of the LDL receptor superfamily (Grant and Hirsh 1999), and accordingly, VITs and their receptor may be regarded as evolutionary ancestors of LDL and its receptor in higher organisms (Matyash et al. 2001).

According to homology screening, C. elegans possesses six genes encoding zinc matrix metalloproteinases (ZMPs) (Wada et al. 1998). Recombinant C. elegans ZMPs have been shown to cleave a MMP peptide substrate and this activity was inhibited by human tissue inhibitor of MMP, suggesting that the catalytic sites of C. elegans ZMPs and human MMPs are structurally closely related (Wada et al. 1998). Investigating the effects of all six C. elegans ZMPs in vivo, we found in a previous study that only RNA-interference (RNAi) for zmp-2 (H19M22.3) resulted in nematodes with moulting defects indicating its role in extracellular matrix degradation during ecdysis (Altincicek et al. 2010). Moreover, knockdown of zmp-2 was associated with reduced survival under heat stress or during infection with the nematode pathogenic bacterium Photorhabdus luminescens (Altincicek et al. 2010). In hermaphroditic adults, the strongest expression of zmp-2 was detectable in the two spermathecae and spermathecal-uterine valves but weaker fluorescence was observed in a zmp-2 promoter::gfp transgenic strain along the intestinal tract (Altincicek et al. 2010).

In the present study, we investigated in C. elegans the impact of RNAi for vit-6 on the reduction of survival caused by zmp-2 RNAi under heat stress.

Materials and methods

Strains and maintenance

Caenorhabditis elegans strains were maintained on nematode growth medium (NGM) agar plates seeded with E. coli OP50 at 20 °C according to standard protocols (Brenner 1974). Caenorhabditis elegans strains wild-type N2, variation Bristol, the mutants DR2281 daf-9(m540), AA1 daf-12(rh257), CF1038 daf-16(mu86), DH1390 rme-2(b1008), the transgenic strain TJ356 zIs356 Is[daf-16::daf-16-gfp; rol-6] and E. coli OP50 were obtained from the C. elegans Genetics Center (University of Minnesota, MN, US). Methods such as freezing nematodes and obtaining synchronous populations using a bleaching method with hypochlorite treatment of egg-laying adults were performed according to standard protocols. RNAi clones were obtained from MRC GeneService Ltd (Cambridge, UK) and included a negative control (L4440), rme-2 (T11F8.3), daf-9 (T13C5.1), daf-12 (F11A1.3), daf-16 (R13H8.1), sir-2.1 (R11A8.4), ftt-2 (F52D10.3) and par-5 (M117.2). The RNAi clone of vit-6 (K07H8.6) was constructed using standard cloning techniques as described elsewhere (Fischer et al. 2012).

RNAi experiments

RNAi experiments were performed in liquid cultures as previously described (Lehner et al. 2006; Timmons et al. 2001; Kamath et al. 2001). In brief, expression of gene-specific dsRNA inside the bacterial RNAi feeding strain E. coli HT115 was induced with 1 mM isopropyl-β-d-thiogalactopyranoside (IPTG) for 1 h at 37 °C to trigger interference. Subsequently, bacterial cells were washed and resuspended in NGM. A volume of 40 μl of this suspension was dispensed in each well of a 96-well plate (Greiner Bio-One, Frickenhausen, Germany), to which 10–15 synchronized L1 larvae were added. In general, L1 larvae reached the adult stage within 3 days of incubation with agitation at 20 °C.

Survival analysis at 37 °C

Nematode survival was determined using a microplate thermotolerance assay as described (Gill et al. 2003). In brief, nematodes were washed off the wells with M9-buffer into 15 ml tubes followed by additional three washing steps. In each well of a black 384-well low-volume microtitre plate (Greiner Bio-One, Frickenhausen, Germany), 6.5 μl M9-buffer/Tween 20 (1 % v/v) solution was added. Subsequently, one nematode was dispensed in 1 μl M9 buffer under a stereomicroscope (Breukhoven Microscope Systems) into each well and mixed with 7.5 μl SYTOX green (final concentration 1 μM; Life Technologies, Karlsruhe, Germany). To prevent water evaporation, the plates were sealed with Rotilabo sealing film and covered with a lid (Greiner Bio-One, Frickenhausen, Germany). Heat shock (37 °C) was induced and fluorescence was measured with the Fluoroskan Ascent fluorometer (Thermo Labsystems, Bonn, Germany) every 30 min. To detect SYTOX green fluorescence, excitation wavelength was set at 485 nm and emission was measured at 538 nm. All experiments determining the lifespan of nematodes at 37 °C were done at least thrice and representative survival curves are shown in the figures.

Quantitative real-time PCR

Total RNA was extracted from 10,000 worms using Trizol (Life Technologies). One-step real-time PCRs were performed in triplicate using 1 µl of RNA template, Brilliant II SYBR Green QRT-PCR Mastermix-Kit (Stratagene Products, Waldbronn, Germany) and appropriate primers in a CFX™ Real-Time PCR Detection System (BioRad, München, Germany). Cycling conditions were 1 × [15 min 50 °C], 1 × [10 min 95 °C], 40 × [30 s 95 °C, 15 s 53 °C, 30 s 60 °C], 1 × [1 min 95 °C], 1 × [30 s 53 °C] and 1 × [1 min 95 °C]. Changes in the target gene expression were calculated according to Pfaffl (2001) using equation 2−ΔΔCT. For each sample, the fold change in the target gene was normalized to 18S rRNA and relative to the control expression. For determination of RNAi efficiency, unique primer pairs (Eurofins MWG Operon, Ebersberg, Germany) recognizing only cDNA derived from endogenous mRNA were designed to avoid cross-reaction with genomic DNA and bacterially generated dsRNA and were as follows: 18S rRNA-fw 5′-ATG GTT GCA AAG CTG AAA CT-3′, 18S rRNA-rev 5′-TCC CGT GTT GAG TCA AAT TA-3′; zmp-2-fw 5′-GCT CAG ATT AGA AGA CGA AG-3′, zmp-2-rev 5′-GAA CTT CAC TTG GAA GAA CA-3′; vit-6-fw 5′-ACC CCA TGC TAC TCC GTT CTC-3′, vit-6-rev 5′-CAA CCT TGA CGT TCT TCC ACT CC-3′; daf-9-fw 5′-TTC TGT CTA GCG TTC TCG-3′, daf-9-rev 5′-CCA AGA ACT TTG GCT TAT GT-3′; daf-12-fw 5′-CAA CGT GGA TGA TAT GTT TG-3′, daf-12-rev 5′-GAA GAA ACC GAA GAA CTC TA-3′; daf-16-fw 5′-CGG AAG GCT TAA ACT CAA TG-3′; daf-16-rev 5′-GAC GGA TCG AGT TCT TCC AT-3′.

Relative mRNA levels in nematodes cultured on RNAi bacteria were significantly lower (p < 0.01) than mRNA levels of the control that was fed L4440 and were below 0.25 for all genes tested.

Western blot

For detection of VIT-6 at the protein level, a YP88 rat-anti-vit-6 polyclonal antibody (kindly provided by Prof. Thomas Blumenthal, University of Colorado) at a 1:5,000 dilution was used and β-actin, as a loading control, was detected with a rabbit-anti-actin polyclonal antibody (Sigma-Aldrich, Hamburg, Germany) at 1:500. As secondary antibodies goat-anti-rat IgG polyclonal (Dianova, Hamburg, Germany) at 1:5,000, and goat-anti-rabbit IgG polyclonal (Santa Cruz, Heidelberg, Germany) at 1:500, respectively, were used as horseradish peroxidase (HRP) conjugate. Groups of 10,000 nematodes were treated with lysis buffer (saccharose 0.8 M, EDTA 1 mM, Tris–HCL 10 mM, PMSF 0.5 mM) and twice freeze-thawed at −80 °C and room temperature, respectively. Lysates were separated on 8.5 % SDS-PAGE gels and proteins were transferred to a polyvinylidene fluoride (PVDF) membrane (Millipore, Schwalbach, Germany) for 1 h at 1.0 mA/cm2 membrane area. The blots were preblocked in 15 ml of 1 % milk in TBS/0.05 % Tween 20 and probed with antibodies diluted in blocking solution for 1 h. Following 2 × 5 min washes with TBS-T and 2 × 5 min TBS, and incubation in enhanced chemiluminescence (ECL) solution, the radiographic film was exposed to detect the immunoreactive bands. Band intensities were quantified using ImageJ (NIH).

Detection of H2O2

Detection of H2O2 was done by the use of the N-acetyl-3,7-dihydroxyphenoxazine (Amplex® Ultra Red, Sigma-Aldrich, Hamburg, Germany) assay. In the presence of H2O2, Amplex® Ultra Red is oxidized by horseradish peroxidase (HRP) to a red-fluorescent oxidation product (Mohanty et al. 1997). To assess the H2O2 production from C. elegans, 700 young adult worms per condition were washed four times with 0.25 M Na2HPO4. Approximately 100 nematodes per 50 µl were transferred into flat-bottomed 96-well plates (Greiner Bio-One, Frickenhausen, Germany) and subsequently 50 µl Amplex® Ultra Red reaction buffer solution (50 µl 10 mM Amplex® Ultra Red, 100 µl HRP; 10 U/ml, 4.85 ml 0.25 M Na2HPO4) was added to each well. After 3-h incubation, fluorescence was measured by the use of the microplate reader with excitation at 550 nm and fluorescence emission detection at 592 nm, respectively.

OxyBlot

The Millipore OxyBlot™ Protein Oxidation Detection Kit was used for immunoblot detection of carbonylated proteins. Therefore, groups of 10,000 nematodes were treated with lysis buffer (0.8 M sucrose, 1 mM EDTA, 10 mM Tris‐HCL, 0.5 mM PMSF), twice freeze-thawed at −80 °C and room temperature, respectively, and subsequently sonicated on ice. The concentration of isolated proteins was adjusted to 1.5 mg/ml before derivatization was performed according to the instruction manual, using 5 µl protein sample. Derivatized proteins were separated by 8.5 % SDS-PAGE and blotted onto a PVDF membrane (1 h, 1.0 mA/cm2). The membrane was blocked with 1 % milk in TBS/0.05 % Tween®20 and probed with antibodies as described in the instruction manual of the OxyBlot kit. β-Actin from non-derivatized samples was detected as a loading control for the normalization of intensities of the bands between the different treatments by the use of a horseradish peroxidase-conjugated goat-anti-rabbit IgG (Santa Cruz, Heidelberg, Germany). For chemiluminescence detection, the membrane was incubated for 1 min with freshly prepared enhanced chemiluminescent solution (1 M Tris pH 8.5, 90 mM p-coumaric acid, 250 mM luminol, 0.01 % H2O2). An autoradiography film was exposed for 5 min to detect immunoreactive bands. Band intensities were quantified using ImageJ (NIH).

Microscopic analyses

To visualize ROS stress located in mitochondria, worms were grown in liquid culture and treated for 24 h at 20 °C in the young adult stage with 0.5 μg/ml MitoTracker CM-H2XRos (Life Technologies). CM-H2XRos produces a ROS-specific staining of mitochondria within cells that is amenable to both qualitative and quantitative measurements of mitochondrial production of H2O2 (Degli Esposti 2002). It does not get fluorescent until it enters an actively respiring cell, where it is oxidized predominantly by reactions involving hydrogen peroxide production (Degli Esposti 2002). According to its positive charge acquired on oxidation by intracellular ROS, the probe covalently binds to mitochondrial proteins and thus produces a permanent organelle-specific stain (Degli Esposti 2002). The MitoTracker fluorescence was measured at 580 nm after excitation at 530–585 nm by the use of an Axioskop 2 epifluorescence microscope (Zeiss, Jena). The microscopic images were generated as 24-bit-jpeg format, which were quantified by using ImageJ (NIH).

Dehydroergosterol (Sigma, Deisehofen, Germany) uptake was measured using the Axioskop2 as described for MitoTracker staining. Therefore, L1 larvae were grown as described for RNAi experiments in the presence of 100 µM dehydroergosterol. Fluorescence was measured after excitations at 340–380 nm and emissions at 425 nm and quantified by using ImageJ (NIH).

Calculations and statistics

Statistical analyses were performed with GraphPad Prism 5.0 software (GraphPad, La Jolla, CA, USA). Log-rank test was performed to compare survival rates under heat stress with p values <0.05 being significant. Kaplan–Meier survival curves are shown for lifespan experiments, which all have been repeated more than once with similar effects. For group comparisons, t test or analysis of variance (ANOVA) was performed. Following ANOVA, differences between groups were determined by Bonferroni-Holm multiple comparison test. Results are presented as mean ± SD.

Results

Vit-6 RNAi blocks the reduction of thermotolerance caused by zmp-2 RNAi

Since ZMPs through alteration of extracellular proteins affect several pathologies associated with reduced stress resistance, we tested here its influence on heat-stress resistance in the model organism C. elegans. Knockdown of zmp-2 was associated with a significant reduction of survival of wild-type nematodes at 37 °C (Fig. 1a). Suggesting that lipoproteins could be a target for ZMP-2, we assessed in how far uptake of lipoproteins into cells plays a role for the zmp-2 RNAi-induced reduction of thermotolerance. Reducing the transcript levels of vit-6 by RNAi was found to be associated with a complete rescue of the lifespan reducing activity exerted by zmp-2 RNAi (Fig. 1a), suggesting that indeed zmp-2 RNAi alters lipoproteins extracellular. Knockdown of rme-2, encoding the VIT-receptor, likewise to the knockdown of vit-6, completely abolished the lifespan reduction caused by knockdown of zmp-2 (Fig. 1b).
Fig. 1

Cholesterol transport is essential for the reduction of survival under heat stress by zmp-2 knockdown. RNAi versus vit-6 completely rescues the lifespan reduction which is due to zmp-2 RNAi in N2 wild-type nematodes (a). The functional loss of a receptor for receptor-mediated endocytosis in the rme-2 mutant prevented the toxicity mediated by zmp-2 RNAi in N2 completely (b)

Vit-6 RNAi increases the ROS burden inside and outside of C. elegans

Since VIT-6 besides its transport-relevant functions displays also antioxidative functions, we were interested in how far its knockdown affects intra- and extracellular ROS levels. RNAi for zmp-2 resulted in an increase of MitoTracker CM-H2XRos fluorescence, indicating increased intracellular ROS (Fig. 2a), enhanced protein carbonyls as a measure of protein oxidation (Fig. 2b), and also an increase of ROS in the extracellular compartment as measured using Amplex Red (Fig. 2c). Although not significantly, all three parameters were further enhanced by additional vit-6 RNAi (Fig. 2a–c), indicating that the unaltered lifespan versus the control under vit-6 and zmp-2 double RNAi occurs in spite of increased ROS stress. To substantiate that extracellular oxidized lipoproteins are responsible for the thermotolerance reducing effects of zmp-2 RNAi, the ROS scavenger ascorbic acid was applied. This reduced the ROS levels in the extracellular mileu of zmp-2 RNAi-treated nematodes to the levels of the control (Fig. 2c) and moreover prevented any effects on survival at 37 °C by zmp-2 RNAi (Fig. 2d). The importance of increasingly accumulating oxidatively modified lipoprotein constituents outside the cells and their transport into the cells as the basis for the reduced thermotolerance caused by zmp-2 RNAi is further substantiated by the reduced expression of vit-6 at the transcript level (Fig. 3a) and also at the protein level (Fig. 3b) when zmp-2 was knocked down. Since under these conditions reduction of survival is fully evident, we suggested that a further restriction of oxidized lipoprotein uptake by vit-6 RNAi will provide protection. As shown, vit-6 RNAi indeed led to a significant lower uptake of the cholesterol homologue DHE than zmp-2 RNAi (Fig. 3c).
Fig. 2

Knockdown of vit-6 increases the ROS stress inside the nematodes. Staining of nematodes using CM-H2XRos demonstrates that ROS stress is increased by zmp-2 RNAi and even more by additional vit-6 RNAi (a). Protein carbonyls were detected by the use of an OxyBlot™ Protein Oxidation Detection Kit (b). Therefore, DNP-derivatized proteins were quantified densitometrically using β-actin as reference. Detection of Amplex Ultra Red fluorescence in the medium subsequent to the incubation of the N2 vector control or nematodes treated with either zmp-2 RNAi or zmp-2 plus vit-6 RNAi revealed an increased ROS secretion in response to both RNAi treatments versus the control (c). Using the ROS scavenger ascorbic acid at a concentration of 100 µM was able to prevent the increase in extracellular ROS due to zmp-2 RNAi (c) and also the reduction of thermotolerance caused by zmp-2 RNAi in wild-type nematodes (d). *p < 0.05; **p < 0.01; *p < 0.001 versus the N2 control

Fig. 3

Zmp-2 RNAi decreases vit-6 expression and DHE uptake. Real-time quantitative PCR (a) and Western blot analysis with β-actin as a loading control (b) show the significantly decreased vit-6 expression at the mRNA and protein level, respectively, in nematodes treated with zmp-2 RNAi. Uptake of dehydroergosterol was measured according to its fluorescent properties using fluorescence microscopy (c) and quantified using ImageJ (c, right lower panel). **p < 0.01; ***p < 0.001 versus the N2 vector control; ## p < 0.01 versus zmp-2 RNAi-treated nematodes

Zmp-2 RNAi reduces survival under heat stress depending on DAF-16 which inhibits DAF-9 and DAF-12

The foxo transcription factor DAF-16 has been shown in many studies to be pivotal for resistance against various kinds of stress. It was astonishing, therefore, that the knockdown of daf-16 was able to reverse the thermotolerance reduction induced by zmp-2 RNAi (Fig. 4a). Since it has been demonstrated that SIR-2.1 and also the 14-3-3 proteins FTT-2 and PAR-5 can function as transcriptional co-activators of DAF-16 (Berdichevsky et al. 2006; Berdichevsky and Guarente 2006), also their impact on survival as affected by zmp-2 RNAi was studied. It was found that likewise to the knockdown of daf-16 also the knockdown of each of the three co-activators prevented any thermotolerance diminishing effect of zmp-2 RNAi (Table 1). Moreover, in zmp-2 RNAi-treated nematodes, DAF-16 was found to be exclusively localized to the nuclei (Fig. 4b).
Fig. 4

DAF-16 mediates the detrimental effects of zmp-2 RNAi. When daf-16 was knocked down by RNAi, zmp-2 RNAi was no longer able to reduce the survival of wild-type C. elegans at 37 °C (a). DAF-16 was exclusively localized in the nuclei after zmp-2 RNAi as was evidenced using the transgenic strain TJ356 expressing DAF-16::GFP (b)

Table 1

RNAi for sir-2.1, ftt-2 or par-5 prevent the reduction of survival under heat stress caused by zmp-2 RNAi

RNAi treatment

Average lifespan ± SD [h]

Number of nematodes

Significance

vector control

9.8 ± 1.3

70

 

zmp-2

7.2 ± 2.3

76

***

sir-2.1

9.3 ± 2.0

76

 

zmp-2/sir-2.1

9.4 ± 1.9

73

#***

ftt-2

9.3 ± 1.4

75

 

zmp-2/ftt-2

9.1 ± 1.1

73

#***

par-5

9.0 ± 1.0

76

*

zmp-2/par-5

8.9 ± 1.1

77

#***

p < 0.05 versus control; *** p < 0.001 versus control; #*** p < 0.001 versus zmp-2 RNAi

In previous studies, we have found that stress resistance against nematode pathogenic bacteria is dependent on the steroid signalling pathway (Fischer et al. 2013) and especially its members DAF-9 and DAF-12 (Rottiers et al. 2006; Gerisch et al. 2001). As a matter of fact, mutants for daf-9 (Fig. 5a) or daf-12 (Fig. 5b) were hypersensitive versus the knockdown of zmp-2. That DAF-16 acts through the inhibition of DAF-9 and DAF-12 was evidenced by the knockdown of daf-16 in either daf-9 or daf-12 mutants. Both mutants no longer responded under zmp-2 RNAi to daf-16 RNAi with an extension of survival at 37 °C (Fig. 5c, d).
Fig. 5

DAF-9 and DAF-12 are required for resistance versus zmp-2 RNAi-mediated toxicity. In nematodes mutant for daf-9 (a) or daf-12 (b) zmp-2 RNAi reduced the thermotolerance to a significant higher extent than in wild-type nematodes. Daf-16 RNAi performed in both mutant strains revealed that the knockdown of the foxo transcription factor is no longer able to prevent the survival reduction as caused by zmp-2 RNAi under subsequent heat stress (c, d). Statistical analysis is only shown for groups treated with zmp-2 RNAi

A basic supply of cholesterol is mandatory for activation of steroid signalling and the increase in thermotolerance under zmp-2 RNAi

The finding that DAF-9 and DAF-12 exerted protective effects to zmp-2 RNAi (Fig. 5a, b) was unexpected, based on the increased nematode survival also under zmp-2 RNAi when delivery of their activator cholesterol was reduced by vit-6 or rme-2 RNAi (Fig. 1). As a matter of fact, however, in both daf-9 and daf-12 mutants vit-6 RNAi exerted no effect on the reduction in thermotolerance caused by zmp-2 RNAi (Fig. 6a, b). We therefore suggested that a basic supply of cholesterol is necessary and possible under vit-6 RNAi in order to enable the activation of the steroid signalling pathway and to prolong the lifespan under zmp-2 knockdown. This hypothesis is supported by the fact that in wild-type nematodes residual intestinal uptake of the cholesterol homologue dehydroergosterol in the presence of vit-6 RNAi is evident (Fig. 3c). Moreover, reducing the cholesterol concentration in the feeding media to 2.5 µg/ml prevented vit-6 RNAi to exert its reverting effects on survival reduction in wild-type nematodes which was due to zmp-2 RNAi (Fig. 6c). Finally, a daf-16 deletion mutant proved to be resistant against zmp-2 RNAi but became hypersensitive when vit-6 was knocked down in addition (Fig. 6d).
Fig. 6

Vit-6 RNAi needs DAF-9 and DAF-12 in order to prevent zmp-2 RNAi-induced reduction of thermotolerance. In daf-9 (a) and daf-12 (b) mutant animals, the knockdown of vit-6 was no longer effective in reverting the zmp-2 RNAi-induced reduction in survival. The suggestion that under vit-6 RNAi low levels of cholesterol are transported in order to trigger DAF-9, and DAF12 is supported by a lack of survival reverting effect of vit-6 RNAi when 2.5 µg cholesterol/ml NGM instead of 5 µg cholesterol/ml NGM were fed (c). Moreover, in daf-16 mutant nematodes, vit-6 RNAi in zmp-2 RNAi treated nematodes reduced survival, indicating the requirement of minimal cholesterol for the vit-6 RNAi-mediated survival extension (d). Statistical analysis is only shown for groups treated with zmp-2 RNAi

Discussion

In the present study, we have shown that knockdown of the zinc matrix metalloproteinase zmp-2 in C. elegans significantly reduces the resistance versus heat stress. Those results are in agreement with findings suggesting that zinc-dependent mechanisms, maybe represented by the activities of MMPs, can be a single mediator in modulating neuroendocrine–thymus interaction in ageing (Mocchegiani et al. 2013). Zmp-2 RNAi caused an increase of intracellular and extracellular ROS, but since reductions of thermotolerance were completely inhibited when transport of lipoproteins was reduced through the knockdown of vit-6, we suggest that transport of oxidized lipoproteins into the cells mediates the effects of zmp-2 knockdown on thermotolerance (Fig. 7). In search of the oxidized compound mediating the reduction in stress resistance, the most plausible explanation would be provided by the oxidation of VIT-6 itself, since it has been demonstrated to be the most abundant oxidized protein in adult nematodes (Nakamura et al. 1999). Indeed protein carbonylation of a 88 kDa protein which could represent VIT-6 was increased by zmp-2 RNAi in our studies. Alternative explanations are that the oxidative mileu caused by zmp-2 RNAi oxidizes other apolipoproteins than VIT-6 or that VIT-6 is just the mediator of transport, e.g. for oxysterols, which are a hallmark of a number of age-related diseases in humans, such as atherosclerosis, neurodegenerative diseases or age-related macular degeneration (Poli et al. 2013). Whatever the stress resistance reducing effector might be, our results make clear that lipoprotein transport essentially mediates the detrimental effects of zmp-2 RNAi, which alternatively could also be prevented by the addition of ascorbic acid. Ascorbic acid reduces the ROS burden at the extracellular site and must act from this compartment since thermotolerance is increased by vit-6 RNAi instead of increased intracellular ROS levels and protein carbonyls.
Fig. 7

Concept explaining the effects of the zinc matrix metalloproteinase ZMP-2 on stress resistance in C. elegans as impaired by the transport of oxidized cholesterol adducts. Extracellular cholesterol can be exploited by the cells subsequent to its transport requiring VIT-6 and RME-2, in order to trigger the steroid signalling pathway. Extracellular ROS, however, can oxidize cholesterol or lipoproteins before their cellular uptake. Once inside the cell, oxidized cholesterol causes a cellular response which involves DAF-16 and consequently inhibits DAF-9 and DAF-12. Those effects are associated with reduced stress resistance and can be prevented either by reducing the uptake of oxidized cholesterol adducts or by ZMP-2, which is suggested to degrade such cytotoxic products

It was surprising to note that the reductions of thermotolerance caused by the knockdown of zmp-2 were completely dependent on the presence of the foxo transcription factor DAF-16, which has been described to transcriptionally trigger several stress response mechanisms in association with longevity (McColl et al. 2010). On the other hand, we have previously demonstrated that the prevention of nuclear DAF-16 localization by VIT-6 is associated with defence mechanisms against a nematode pathogen (Fischer et al. 2013) demonstrating that enhanced resistance, as achieved, e.g. by the prevention of faulty water homoeostasis (Evans et al. 2008), can also derive from the absence of transcriptional activity of DAF-16. Here, however, it is not that the absence of DAF-16 transcriptional activity provides stress resistance but that its nuclear localization is found to be associated with the survival reductions caused by zmp-2 RNAi. That indeed the zmp-2 RNAi effects on thermotolerance are mediated through transcriptional activity of DAF-16 is further stressed by the fact that the knockdown of its transcriptional co-activators sir-2.1, ftt-2 and par-5 (Berdichevsky et al. 2006; Berdichevsky and Guarente 2006) prevented the reduced thermotolerance as caused by zmp-2 RNAi in an identical manner as daf-16 RNAi.

Besides the insulin signalling pathway with its key factor DAF-16, the steroid signalling pathway including its key components DAF-9, a cytochrome P450-dependent enzyme forming dafachronic acids, and the nuclear hormone receptor DAF-12, recognizing dafachronic acids as ligands, has been shown to exert significant effects on lifespan and survival (Rottiers et al. 2006; Gerisch et al. 2001). Also in this regard, the picture is not completely clear, given that dafachronic acid supplementation shortened the lifespan of long-lived daf-9 mutants and abolished their stress resistance, whereas they extended the lifespan of germ-line ablated daf-9 mutants, demonstrating that the steroid signalling pathway may regulate C. elegans lifespan according to signalling state (Gerisch et al. 2007). In the present study, we demonstrate that both DAF-9 and DAF-12 are involved in the protection against the toxicity mediated by zmp-2 RNAi (Fig. 7). Strains mutant for either daf-9 or daf-12 were hypersensitive to zmp-2 RNAi. Moreover, in these strains, daf-16 RNAi no longer provided any protection from zmp-2 RNAi, demonstrating that both factors act downstream from DAF-16 and are inhibited by the foxo transcription factor (Fig. 7).

Since cholesterol, however, provides the substrate for steroid signalling, it has to be assumed that a minimal supply of sterols is mandatory in order to enable DAF-9 to generate ligands for DAF-12 and to compensate for the detrimental effects of zmp-2 RNAi (Fig. 7). This hypothesis is substantiated by the results obtained in wild-type nematodes which were fed low cholesterol concentrations because they did not respond with an extended survival when vit-6 was knocked down in zmp-2 RNAi exposed nematodes. Also the daf-16 RNAi-mediated resistance to the reductions of survival by zmp-2 RNAi proved to be dependent on an adequate minimal cholesterol supply since double RNAi for zmp-2 and vit-6 reduced the survival of daf-16 mutants dramatically.

In conclusion, we provide evidence that ZMP-2 in C. elegans prevents the accumulation of oxidized lipoproteins containing VIT-6 which are absorbed into the nematodes by receptor-mediated endocytosis. A lack of ZMP-2 activity leads to the absorption of toxic adducts which then trigger DAF-16 to inhibit DAF-9 and DAF-12 and lead to diminished thermotolerance.

Declarations

Conflict of interest

None.

Authors’ Affiliations

(1)
Molecular Nutrition Research, Interdisciplinary Research Centre, Justus-Liebig-University of Giessen

References

  1. Altincicek B, Fischer M, Lüersen K, Boll M, Wenzel U, Vilcinskas A (2010) Role of matrix metalloproteinase ZMP-2 in pathogen resistance and development in Caenorhabditis elegans. Dev Comp Immunol 34:1160–1169PubMedView ArticleGoogle Scholar
  2. Badimon L, Storey RF, Vilahur G (2011) Update on lipids, inflammation and atherothrombosis. Thromb Haemost 105:S34–S42PubMedView ArticleGoogle Scholar
  3. Baker ME (1988) Is vitellogenin an ancestor of apolipoprotein B-100 of human lowdensity lipoprotein and human lipoprotein lipase? Biochem J 255:1057–1060PubMed CentralPubMedGoogle Scholar
  4. Berdichevsky A, Guarente L (2006) A stress response pathway involving sirtuins, forkheads and 14-3-3 proteins. Cell Cycle 5:2588–2591PubMedView ArticleGoogle Scholar
  5. Berdichevsky A, Viswanathan M, Horvitz HR, Guarente L (2006) C. elegans SIR-2.1 interacts with 14-3-3 proteins to activate DAF-16 and extend lifespan. Cell 125:1165–1177PubMedView ArticleGoogle Scholar
  6. Branicky R, Desjardins D, Liu JL, Hekimi S (2010) Lipid transport and signaling in Caenorhabditis elegans. Dev Dyn 239:1365–1377PubMedGoogle Scholar
  7. Brenner S (1974) The genetics of Caenorhabditis elegans. Genet Dev 77:71–94Google Scholar
  8. Chitwood DJ, Lusby WR (1991) Metabolism of plant sterols by nematodes. Lipids 26:619–627PubMedView ArticleGoogle Scholar
  9. Degli Esposti M (2002) Measuring mitochondrial reactive oxygen species. Methods 26:335–340PubMedView ArticleGoogle Scholar
  10. Evans EA, Kawli T, Tan MW (2008) Pseudomonas aeruginosa suppresses host immunity by activating the DAF-2 insulin-like signaling pathway in Caenorhabditis elegans. PLoS Pathog 4:1000175View ArticleGoogle Scholar
  11. Fischer M, Regitz C, Kahl M, Werthebach M, Boll M, Wenzel U (2012) Phytoestrogens genistein and daidzein affect immunity in the nematode Caenorhabditis elegans via alterations of vitellogenin expression. Mol Nutr Food Res 56:957–965PubMedView ArticleGoogle Scholar
  12. Fischer M, Regitz C, Kull R, Boll M, Wenzel U (2013) Vitellogenins increase stress resistance of Caenorhabditis elegans after Photorhabdus luminescens infection depending on the steroid-signaling pathway. Microbes Infect 15:569–578PubMedView ArticleGoogle Scholar
  13. Gerisch B, Weitzel C, Kober-Eisermann C, Rottiers V, Antebi A (2001) A hormonal signaling pathway influencing C. elegans metabolism, reproductive development, and life span. Dev Cell 1:841–851PubMedView ArticleGoogle Scholar
  14. Gerisch B, Rottiers V, Li D, Motola DL, Cummins CL, Lehrach H, Mangelsdorf DJ, Antebi A (2007) A bile acid-like steroid modulates Caenorhabditis elegans lifespan through nuclear receptor signaling. Proc Natl Acad Sci 104:5014–5019PubMed CentralPubMedView ArticleGoogle Scholar
  15. Gill MS, Olsen A, Sampayo JN, Lithgow GJ (2003) An automated high-throughput assay for survival of the nematode Caenorhabditis elegans. Free Radic Biol Med 35:558–565PubMedView ArticleGoogle Scholar
  16. Grant B, Hirsh D (1999) Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte. Mol Biol Cell 10:4311–4326PubMed CentralPubMedView ArticleGoogle Scholar
  17. Hernández-Pérez M, Mahalingam M (2012) Matrix metalloproteinases in health and disease: insights from dermatopathology. Am J Dermatopathol 34:565–579PubMedView ArticleGoogle Scholar
  18. Kamath RS, Martinez-Campos M, Zipperlen P, Fraser AG, Ahringer J (2001) Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans. Genome Biol 2:RESEARCH0002Google Scholar
  19. Lehner B, Tischler J, Fraser AG (2006) RNAi screens in Caenorhabditis elegans in a 96-well liquid format and their application to the systematic identification of genetic interactions. Nat Protoc 1:1617–1620PubMedView ArticleGoogle Scholar
  20. Lund AK, Lucero J, Harman M, Madden MC, McDonald JD, Seagrave JC, Campen MJ (2011) The oxidized low-density lipoprotein receptor mediates vascular effects of inhaled vehicle emissions. Am J Respir Crit Care Med 184:82–91PubMed CentralPubMedView ArticleGoogle Scholar
  21. Matyash V, Geier C, Henske A, Mukherjee S, Hirsh D, Thiele C, Grant B, Maxfield FR, Kurzchalia TV (2001) Distribution and transport of cholesterol in Caenorhabditis elegans. Mol Biol Cell 12:1725–1736PubMed CentralPubMedView ArticleGoogle Scholar
  22. McColl G, Rogers AN, Alavez S, Hubbard AE, Melov S, Link CD, Bush AI, Kapahi P, Lithgow GJ (2010) Insulin-like signaling determines survival during stress via posttranscriptional mechanisms in C. elegans. Cell Metab 12:260–272PubMed CentralPubMedView ArticleGoogle Scholar
  23. Mocchegiani E, Malavolta M, Costarelli L, Giacconi R, Piacenza F, Lattanzio F, Basso A (2013) Is there a possible single mediator in modulating neuroendocrine-thymus interaction in ageing? Curr Aging Sci 6:99–107PubMedView ArticleGoogle Scholar
  24. Mohanty JG, Jaffe JS, Schulman ES, Raible DG (1997) A highly sensitive fluorescent micro-assay of H2O2 release from activated human leukocytes using a dihydroxyphenoxazine derivative. J Immunol Methods 202:133–141PubMedView ArticleGoogle Scholar
  25. Nakamura A, Yasuda K, Adachi H, Sakurai Y, Ishii N, Goto S (1999) Vitellogenin-6 Is a Major Carbonylated Protein in Aged Nematode, Caenorhabditis elegans. Biochem Biophys Res Commun 264:580–583PubMedView ArticleGoogle Scholar
  26. Page-McCaw A, Ewald AJ, Werb Z (2007) Matrix metalloproteinases and the regulation of tissue remodelling. Nat Rev Mol Cell Biol 8:221–233PubMed CentralPubMedView ArticleGoogle Scholar
  27. Pfaffl MW (2001) A new mathematical model for relative quantification in real-time T-PCR. Nucleic Acids Res 92:2002–2007Google Scholar
  28. Poli G, Biasi F, Leonarduzzi G (2013) Oxysterols in the pathogenesis of major chronic diseases. Redox Biol 1:125–130PubMed CentralPubMedView ArticleGoogle Scholar
  29. Rottiers V, Motola DL, Gerisch B, Cummins CL, Nishiwaki K, Mangelsdorf DJ, Antebi A (2006) Hormonal control of C. elegans dauer formation and life span by a Rieske-like oxygenase. Dev Cell 10:473–482PubMedView ArticleGoogle Scholar
  30. Shin MH, Moon YJ, Seo JE, Lee Y, Kim KH, Chung JH (2008) Reactive oxygen species produced by NADPH oxidase, xanthine oxidase, and mitochondrial electron transport system mediate heat shock-induced MMP-1 and MMP-9 expression. Free Radic Biol Med 44:635–645PubMedView ArticleGoogle Scholar
  31. Siefert SA, Sarkar R (2012) Matrix metalloproteinases in vascular physiology and disease. Vascular 20:210–216PubMedView ArticleGoogle Scholar
  32. Timmons L, Court DL, Fire A (2001) Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans. Gene 263:103–112PubMedView ArticleGoogle Scholar
  33. Vu TH, Werb Z (2000) Matrix metalloproteinases: effectors of development and normal physiology. Genes Dev 14:2123–2133PubMedView ArticleGoogle Scholar
  34. Wada K, Sato H, Kinoh H, Kajita M, Yamamoto H, Seiki M (1998) Cloning of three Caenorhabditis elegans genes potentially encoding novel matrix metalloproteinases. Gene 211:57–62PubMedView ArticleGoogle Scholar

Copyright

© Springer-Verlag Berlin Heidelberg 2014

Advertisement