- Open Access
SerpinA3N is a novel hypothalamic gene upregulated by a high-fat diet and leptin in mice
Genes & Nutritionvolume 13, Article number: 28 (2018)
Energy homeostasis is regulated by the hypothalamus but fails when animals are fed a high-fat diet (HFD), and leptin insensitivity and obesity develops. To elucidate the possible mechanisms underlying these effects, a microarray-based transcriptomics approach was used to identify novel genes regulated by HFD and leptin in the mouse hypothalamus.
Mouse global array data identified serpinA3N as a novel gene highly upregulated by both a HFD and leptin challenge. In situ hybridisation showed serpinA3N expression upregulation by HFD and leptin in all major hypothalamic nuclei in agreement with transcriptomic gene expression data. Immunohistochemistry and studies in the hypothalamic clonal neuronal cell line, mHypoE-N42 (N42), confirmed that alpha 1-antichymotrypsin (α1AC), the protein encoded by serpinA3, is localised to neurons and revealed that it is secreted into the media. SerpinA3N expression in N42 neurons is upregulated by palmitic acid and by leptin, together with IL-6 and TNFα, and all three genes are downregulated by the anti-inflammatory monounsaturated fat, oleic acid. Additionally, palmitate upregulation of serpinA3 in N42 neurons is blocked by the NFκB inhibitor, BAY11, and the upregulation of serpinA3N expression in the hypothalamus by HFD is blunted in IL-1 receptor 1 knockout (IL-1R1−/−) mice.
These data demonstrate that serpinA3 expression is implicated in nutritionally mediated hypothalamic inflammation.
Once considered problematic for only the Western, developed world, the burden of obesity today encompasses most countries , with shifts in global eating patterns causing detrimental changes in body weight and composition, associated diseases and decreased quality of life [2, 3]. The development of effective treatments for obesity has not been fruitful, with the continued futility of dieting methodologies for sustained weight loss, and gastric surgery being the only current long-term solution [4,5,6], putting health care systems under an enormous amount of pressure. In order for more effective, preventative measures to be put in place, it is crucial to understand the mechanisms that cause obesity. The overconsumption of energy-dense foods, particularly those high in long-chain saturated fat and sugar, appears to be a primary driving force behind the obesity epidemic . These foods have been shown to have a powerful effect on the hypothalamus in rodent models, resulting in inflammation and astrogliosis that is implicated in diet-induced obesity [8,9,10].
Energy balance, food intake and consequently body weight are effectively regulated by a well-defined and complex hypothalamic system. Briefly, two distinct types of neurons have been identified as important in energy balance regulation: orexigenic neurons expressing neuropeptide Y (NPY) and agouti-related peptide (AgRP) and anorexigenic neurons expressing proopiomelanocortin (POMC) and cocaine- and amphetamine-regulated transcript (CART). Both orexigenic and anorexigenic neurons express leptin receptors, highlighting the importance of this hormones in the system. Leptin acts on multiple levels in hypothalamic neurons, effecting gene transcription, post-translational processing as well as membrane polarisation to inhibit AgRP/NPY neurons while activating POMC/CART neurons, resulting in a stable body weight . In the obese state, the ability of leptin to regulate feeding behaviour as well as peripheral glucose homeostasis is diminished as a result of hypothalamic insensitivity to this hormone [12,13,14,15,16].
When animals are fed a high-fat diet (HFD), they ingest more energy than they expend, resulting in increased adiposity, and eventually obesity, suggesting that a HFD compromises the hypothalamic systems that regulate food intake. This has been confirmed in a number of rodent studies showing that a HFD induces inflammation in the hypothalamus activating microglia, astrocytes and neurons via a Toll-like receptor 4 (TLR4)-dependent mechanism [17,18,19] and the IKKβ/NFκB and JNK inflammatory pathways [20,21,22,23,24] resulting in leptin and insulin insensitivity. Blocking or inhibiting inflammation in the hypothalamus prevents leptin and insulin insensitivity and obesity induced by a HFD [22, 23, 25, 26].
In order to further explore the mechanisms linking HFD to hypothalamic dysfunction and leptin insensitivity, we carried out a microarray-based transcriptomics experiment to determine gene expression changes in response to a HFD as well as leptin challenge. One of the genes that was considerably upregulated by both leptin and HFD was serpinA3N, the gene encoding the anti-protease, alpha-1-antichymotrypsin (α1AC). In the periphery, α1AC is an acute phase protein produced by hepatocytes  and has been recently identified as a marker of reactive astrogliosis in the brain . Increased levels of α1AC in the brain are commonly associated with inflammatory conditions such as Alzheimer’s disease [29, 30].
In the present study we identified, using transcriptomics, that the gene, serpinA3n, is highly expressed in the hypothalamus and is upregulated by leptin and HFD, a finding confirmed by semi-quantitative in situ hybridisation. Furthermore, we have shown that nutritional factors, as well as time on experiment, play a role in the hypothalamic nuclei-specific regulation of serpinA3N expression. As the expression of serpinA3N in the periphery has been reported to be dependent on inflammation and IL-1 stimulation [31,32,33,34], we tested the effect of HFD on hypothalamic serpinA3N expression in IL-1 receptor 1 knockout mice (IL-1R1−/−) and in the hypothalamic clonal neuronal cell line, mHypoE-N42 (N42) which we challenged with oleic and palmitic acid, the latter, with and without blocking the NFκB pathway. In IL-1R1−/− mice, HFD challenge failed to upregulate serpinA3N expression in contrast to wild-type mice and in N42 cells oleic acid downregulated serpinA3N while palmitate upregulated expression which was negated by inhibiting the NFκB pathway, confirming that HFD-induced expression is dependent on inflammation. Also, as increased serpinA3N expression in the brain has previously been identified as a marker of astrocyte activation , we examined α1AC immunoreactivity in the hypothalamus together with that of glial fibrillary acidic protein (GFAP), an astrocyte marker, ionised calcium binding adaptor molecule 1 (Iba1), a microglial marker, and NPY and AgRP, markers of neurons important in energy balance. Immunoreactive α1AC cells were larger and dissimilar to astrocytes and microglia having a distinctive neuronal shape and close associations with NPY and AgRP beaded fibres, also pointing to neuronal expression of serpinA3N. In addition, using Western blotting, the protein product of serpinA3N, α1AC, was detected in N42 neurons in much lower levels than that found in the media demonstrating that the protein is secreted. The expression of serpinA3N in and the secretion of α1AC from these cells confirmed neuronal expression of serpinA3N.
Transcriptomic data revealed the regulation of serpinA3N gene expression in total dissected hypothalamic tissue from mice maintained on a LFD or HFD for 1 or 4 weeks and either challenged with vehicle or leptin. A three-way ANOVA showed significant effects of HFD (P = 0.0007), leptin challenge (P = 2.55 × 10−6), and time on diet (P = 1.34 × 10−6). However, there was no interaction between these factors (Fig. 1). A full list of changed genes can be found at NCBI’s Gene Expression Omnibus and is accessible through GEO Series accession number GSE113943 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi).
Localisation of serpinA3N and α1AC in the hypothalamus
In situ hybridisation using a serpinA3N-specific riboprobe revealed specific labelling throughout the hypothalamus with particularly high levels of expression in the arcuate nuclei (ARC), ventromedial (VMH) and dorsomedial nuclei (DMH). The labelling extended out to the edges of the lateral hypothalamus (LH) (Fig. 2a). Immunoreactive α1AC in the ARC of the hypothalamus revealed a neuronal morphology (Fig. 2b–e). Dual staining using an anti-mouse α1AC antibody (brown) alongside blue anti-GFAP (astrocyte specific) and anti-Iba1 (microglia specific) staining showed smaller and distinctly different cell morphologies with closely associated but not overlapping staining (Fig. 2b, c). Staining with both anti-NPY and anti-AgRP (blue) showed beaded fibres closely associated with anti-α1AC-positive neurons (brown) (Fig. 2d, e).
Regulation of serpinA3N and expression by HFD and time
A robust increase in labelling was seen after just 1 week on a HFD. It was possible to distinguish distinct hypothalamic nuclei which expressed high levels of serpinA3N including the ARC, VMH, DMH, and LH (Fig. 3a, b). Quantification of hypothalamic nuclei including the ARC, VMH, DMH (Fig. 3c–e) and LH (not shown) confirmed the increase in serpinA3N gene expression by a HFD seen in transcriptomics studies. Expression in the ARC was significantly increased by around 50% after 4 weeks on the HFD compared to LFD control (Fig. 3c). In comparison, the level of gene expression in the VMH and DMH was increased by approximately 2.5 and 4 times after only 1 week, respectively. After 16 weeks on the HFD, the labelling in these nuclei had increased to approximately eight times of that seen in LFD fed mice at week 1 (Fig. 3d, e). Analysis of the gene expression data by two-way ANOVA confirmed that serpinA3N gene expression increased with time on the diet and there was no interaction between diet and time for the ARC and DMH but there was for the VMH (P < 0.05) indicating that the age of the animals may also lead to increases in serpinA3N gene expression in the ARC, VMH and DMH over the 16 weeks of the experiment (Fig. 3c–e).
Regulation of serpinA3N expression by leptin
To further investigate the regulation of serpinA3N by leptin, in situ hybridisation was carried out on both leptin-deficient mice (ob/ob) and mice lacking functional leptin receptors (db/db) and their lean littermates (Fig. 4a–d). Images from ob/ob, db/db and lean mice show a much lower level of serpinA3N gene expression in ob/ob and db/db mice (Fig. 4a, b). Quantification of labelling showed a difference of the order of seven to ten times lower levels of gene expression in db/db and ob/ob mice compared to their lean littermates (Fig. 4c, d).
Treatment of ob/ob mice with leptin (10 mg/ml injected IP) resulted in a time-dependent increase in serpinA3N expression with a 10-fold increase within 1 h and a 14-fold increase after 4 h (Fig. 4e). While leptin challenge in lean mice did not increase serpinA3N levels of expression above basal after 1 h, leptin challenge did increase levels of expression significantly after 4 h but only by approximately 70% (Fig. 4f) compared to the 14-fold increase seen in ob/ob mice 4 h after leptin challenge.
Regulation of serpinA3N expression by HFD in the absence of leptin
Transcriptomics data indicated that the effects of leptin and HFD were independent. To confirm this, ob/ob mice, lacking leptin, were fed either a LFD (10% of calories from fat), or a HFD (45% or 60% of calories from fat). The HFD led to a large increase in serpinA3N gene expression compared to the LFD in the nuclei expressing the gene. Quantification of labelling showed an increase of around 20–30 times in both the ARC and the VMH after 8 weeks on a HFD (Fig. 5a, b).
Regulation of serpinA3N expression by fasting and refeeding
In mice fasted for 24 h, serpinA3N expression increased throughout the hypothalamus. Expression increased by around 40% in the ARC and 200% in the VMH. Refeeding the mice for 24 h returned levels of expression to those seen in the fed animals (Fig. 6a, b).
Regulation of serpinA3N by HFD in IL-1R1 −/− mice
Feeding IL-1R1−/− mice, a HFD for 8 weeks appeared to increase serpinA3N by a relatively small amount in the ARC, VMH and DMH compared to the effects seen in wild-type mice. There was substantial variability in the response to the HFD which failed to reach statistical significance (Fig. 7a–c).
Regulation of SerpinA3N in N42 cultured hypothalamic neurons
Leptin challenge upregulated serpinA3N gene expression by twofold compared to vehicle-treated N42 neurons. IL-6 and TNFα were also upregulated. A similar effect was induced by 200 μM palmitic acid. In comparison, 200 μM oleic acid downregulated the gene expression of all three genes (Fig. 8a–c). The upregulation of serpinA3N, IL-6 and TNFα gene expression by palmitate was significantly reduced in the presence of the NFκB inhibitor, BAY11 (Fig. 8d–f).
α1AC secretion from N42 cultured neurons
SDS-PAGE gels of media from cultured N42 neurons showed the presence of several protein bands of different molecular weights but not in cell free media (Fig. 9). Using Western blotting, cell free media displayed extremely faint immunoreactive α1AC bands but culture media from N42 neurons showed two immunoreactive bands, the lower at 59 kDa corresponding to the molecular weight of α1AC (positive control). The band above may correspond to a different post-translationally modified form of the protein. The cell lysate in contrast showed only extremely faint immunoreactive bands including one at 59 kDa (Fig. 9).
Hypothalamic inflammation in response to a HFD in rodents is well-documented after both short- and long-term exposure to HFD [17,18,19, 35, 36]. In the present study transcriptomics data show that, a so far unreported gene, associated with inflammation in the periphery, serpinA3N, is strongly upregulated by HFD and leptin in the hypothalamus. An incidental finding is that serpinA3N is also upregulated by time on experiment which corresponds to the increasing age of the mice. Surprisingly, these effects were largely independent of one another indicating that while hypothalamic serpinA3N expression is regulated by a number of factors these appear to act via independent pathways.
It can be difficult to differentiate between the effects of a HFD and that of diet-induced obesity as the former rapidly leads to the latter. In the present study, the effects of obesity and a HFD are separated in obese ob/ob mice, which, though obese, normally have relatively low levels of hypothalamic serpinA3N gene expression, but when challenged with a HFD, the level of expression is rapidly upregulated demonstrating that the level of serpinA3N expression is regulated by a HFD rather than obesity per se. Also, the possibility that increased caloric intake rather than diet composition is responsible for the upregulation of serpinA3N cannot be ruled out completely in our animal studies. However, ob/ob mice are hyperphagic, but as noted above, they express relatively low levels of hypothalamic serpinA3N when not exposed to a HFD. Additionally, the pro-inflammatory long-chain saturated fat, palmitic acid, upregulates expression of serpinA3N in the clonal neuronal cell line N42, while oleic acid, an anti-inflammatory monounsaturated fatty acid, decreases gene expression indicating that fatty acids have a direct effect on serpinA3N expression in neurons, supporting the contention that serpinA3N expression responds to the increased long-chain saturated fat in the diet rather than to increased caloric intake.
In the periphery, α1AC, the protein encoded by serpinA3N, serves as an acute phase protein produced by the liver, in response to inflammation and binds to proteases, thus limiting inflammation-related damage [37, 38]. In the brain, α1AC has been shown to be associated with inflammation and elevated levels are found in Alzheimer’s disease, closely linked with amyloid plaques [38,39,40]. Other observed functions of peripheral α1AC include inhibition of oxygen uptake and superoxide generation in granulocytes , DNA binding independent of its anti-protease activity, regulation of its own gene expression, and inhibition of DNA polymerase and DNA primase activity [42, 43]. However, the target protein for, and the function of, α1AC in the hypothalamus remains to be identified.
In the present study, in situ hybridisation revealed a widespread localisation of serpinA3N expression throughout the hypothalamus in a pattern corresponding to major nuclei indicating that the expression is neuronal. This is further supported by immunohistochemistry where dual immunostaining for α1AC and both the astrocyte marker, GFAP, and the microglial marker Iba1 reveal no overlap in staining and immunopositive α1AC show a characteristic neuronal shape which is both larger and distinctly different from that of GFAP and Iba1 immunopositive cells. Dual staining with NPY and AgRP shows close associations between α1AC immunopositive fibres and NPY and AgRP beaded fibres. Also, in N42 clonal neurons in culture, which have been used previously to investigate hypothalamic control mechanisms , the expression of serpinA3N is upregulated by both leptin and palmitate in a manner consistent with that seen in the hypothalamus in response to leptin challenge and a HFD. Taking all of this evidence together, serpinA3N measured in the present study appears largely neuronal in origin. Nonetheless, in a previous genomic study involving two mouse models of brain injury (ischemic stroke and neuroinflammation), serpinA3N was identified as a marker of reactive astrogliosis , and as HFD has been shown to induce astrogliosis in mice [17, 45], then potentially, some of the increase in serpinA3N expression may be astrocytic. Thus, we cannot rule out that part of the increased gene expression seen may occur in astrocytes.
In the liver, increased levels of serpinA3N gene expression and subsequently increased levels of α1AC, like all acute phase proteins, are stimulated by inflammation, particularly by raised circulating levels of IL-6 and IL-1 type cytokines working via STAT3 activation and increased NFκB . In N42 neurons, both IL-6 and TNFα were upregulated in parallel with serpinA3N by leptin and palmitic acid, with palmitic acid stimulated gene expression inhibited by BAY11 blocking the NFκB pathway. These results together with the lack of HFD-induced serpinA3N upregulation in IL-1R1−/− mice clearly indicated that hypothalamic serpinA3N is involved in the inflammatory response as in the periphery.
Leptin stimulates the release of IL-1β in the hypothalamus  while a HFD does not appear to upregulate IL-1β in this brain area  but IL-1β does increase in the periphery in obesity  indicating a more complex relationship between HFD, IL-1β and serpinA3N upregulation. Circulating interleukins do not readily cross the blood-brain barrier but influence the brain via intermediate mechanisms . The source of the interleukins and the mechanisms underlying upregulation of serpinA3N expression by a HFD requires further investigation. While there is no significantly different upregulation of serpinA3N gene expression in IL-1R1−/− mice, there is an indication of a variable response to HFD which may be due to increases in circulating leptin levels in response to increasing adiposity and, thus, increasing leptin levels.
While in the absence of leptin, signalling levels of serpinA3N expression in the hypothalamus are low and leptin challenge upregulates serpinA3N expression, the localisation and pattern of leptin-stimulated expression differs from that induced by a HFD. Leptin-induced serpinA3N expression increases mainly in the ARC, VMH and throughout the hypothalamus up to the borders of the LH with no clear demarcation of hypothalamic nuclei other than the ARC and VMH. The role of leptin in the stimulation of serpinA3N expression on a HFD, however, appears to be relatively small as a HFD upregulates serpinA3N gene expression to a much greater degree in ob/ob mice, in the absence of leptin, compared to lean mice in the presence of leptin. The reasons for this are not clear, but counterintuitively, it may be that the presence of leptin is somehow protective against the induction of serpinA3N gene expression by a HFD. Leptin receptors are present on both neurons and astrocytes and leptin may be upregulating serpinA3N in either or both these cell types , with the upregulation of serpinA3N in N42 hypothalamic neurons confirming the neuronal regulation of serpinA3N by leptin. Nonetheless, circulating leptin levels do not appear to be a major regulator of serpinA3N gene expression in the fasting and refed states as the regulation or serpinA3N occurs in opposition to circulating leptin levels, with fasting, which causes leptin levels to drop, increasing serpinA3N gene expression, while refeeding, which increases circulating leptin levels , results in decreased serpinA3N gene expression. However, this may be explained by the stimulation of serpinA3N gene expression by the increased levels of circulating free fatty acids which occur during fasting .
Leptin insensitivity, induced by a HFD, is well documented . While this concept was not specifically tested in the present study, the transcriptomics data which combined leptin challenge on a LFD and HFD indicated that the effect of diet was separate from that of leptin challenge and that there was no interaction between the two indicating that upregulation of serpinA3N gene expression by leptin is unaffected by HFD; however, this remains to be specifically tested.
Increased time on experiment or age of the mice also appears to be a factor in the upregulation of serpinA3N gene expression in the ARC, VMH and DMH of the hypothalamus. Although the effects of extreme ageing were not investigated in the present study, the mice were older at the end of both the transcriptomics and the in situ hybridisation studies on HFD than at the beginning and both showed a clear effect on serpinA3N gene expression with time despite being measured by different approaches. The mice exposed to the HFD for the longest period of time varied in age between 12 weeks at the beginning of the study and 28 weeks at the end on the study. Twelve weeks of age corresponds to a young mature adult, and 28 weeks corresponds to early middle age with mice showing some signs of age-related changes . Ageing has also been reported to induce inflammation in the hypothalamus via the IKKβ/NFκB pathway. Indeed, hypothalamic inflammatory changes have shown to control systemic ageing demonstrating the importance of this phenomenon to the health of the whole organism .
We have shown the upregulation of a novel hypothalamic gene, serpinA3N, by HFD and leptin. Increasing age and fasting also resulted in an upregulation although to a lesser extent. The upregulation of serpinA3N expression by leptin and palmitic acid was confirmed in N42 neurones in culture along with the upregulation of IL-6 and TNFα, two classical markers of inflammation. Blocking the NFκB inflammatory pathway by BAY11 not only prevented the upregulation of IL-6 and TNFα, but also that of serpinA3N. The protein product of serpinA3N, α1AC, is found in the media from cultured N42 neurons but is difficult to visualise within the cell lysate indicating that α1AC is a secreted protein in the hypothalamus as it is in the periphery.
These data strongly support the contention that serpinA3N expression is a marker of inflammation in the hypothalamus regulated by nutritional status and leptin and indicate a potential role for α1AC in hypothalamic inflammation and the regulation of energy balance.
All experiments were carried out according to the institutional and national guidelines of the European Convention of Vertebrate Animals Used for Experimentation, under European Council Directive 86/609/EEC dated November 1986. For the transcriptomics studies, male, 16-week-old, C57BL/6J mice were obtained from Charles River laboratories (Maastricht, The Netherlands) and housed in pairs in the light- and temperature-controlled animal facility of Wageningen University (12:12-h light/dark cycle at 22 °C). Mice were maintained for 1 or 4 weeks on either a HFD (45% kCal from fat) or LFD (10% kCal from fat) (Research Diet Services BV, Wijk bij Duurstede, The Netherlands) modelled on (D12451 and D12450B respectively Research Diets, NJ, USA). (Please see https://researchdiets.com/opensource-diets/dio-series-diets for diet composition details). For this study, palm oil was used in place of lard. They were then challenged with three intraperitoneal (IP) injections of murine leptin (2 mg/kg body weight) (R&D Systems, Abingdon, UK) or carrier at 24, 15 and approximately 3 h prior to killing in the early morning (n = 10). This experiment was part of the NuGO Proof of Principle studies as previously described .
To further investigate the regulation of serpinA3N gene expression on a HFD, male C57BL/6J mice (Harlan, Bicester, UK), aged 12 weeks, were singly housed on grid floors and fed either a HFD (60% kCal from fat) or a LFD (10% kCal from fat) (D12452 and D12450B respectively, Research Diets, NJ, USA—see web site above for detailed dietary breakdown), ad libitum for 3 days, 1, 4, 8, 12 or 16 weeks and killed either by exsanguination or by perfusion fixation (1 week) with 4% paraformaldehyde in phosphate buffered saline (PBS) under terminal anaesthesia (n = 6). To further investigate the upregulation of serpinA3N by leptin, male mice on the C57BL/6J background either leptin deficient (ob/ob) or lacking functional leptin receptors (db/db) and their lean littermates (Harlan, Bicester, UK) were killed for in situ hybridisation (n = 6). Leptin-deficient ob/ob mice and lean littermates (n = 6) were also challenged with vehicle or leptin by intraperitoneal (IP) injection (2 mg/kg body weight) and killed either 1 or 4 h later as detailed above. Food intake in response to leptin was not measured at this time because any changes were deemed to be impractical to measure with any accuracy due to the fact that leptin challenge was carried out over such a short period of time during the light period when food intake is already low. To confirm the upregulation of serpinA3N expression by HFD is independent from that of leptin, ob/ob mice were fed either a LFD 10% kCal from fat or a HFD either 45% or 60% kCal from fat in the form of lard (diets detailed above) for 8 weeks prior to killing by exsanguination.
To test the effect of nutritional status on hypothalamic serpinA3N gene expression, C57BL/6J mice were fasted for 24 h or fed ad libitum on standard mouse diet prior to killing. Refed animals were allowed access to food ad libitum for a period of 24 h after fasting (n = 8).
To test the possibility that inflammation plays a role in the effect of HFD on the expression of serpinA3N, mice from IL-1R1−/− breeding pairs, on C57BL/6J background, purchased from Jackson laboratories were bred at University College Dublin (UCD) for 6–10 generations under specific pathogen-free conditions. Male IL-1R1−/− mice were then fed HFD, 45% kCal or LFD, 10% kCal from fat for 12 weeks prior to killing (D12451 and D12450B respectively, Research Diets, NJ, USA). In this study, palm oil was used instead of lard (n = 9 HFD and n = 5 chow).
Hypothalami were dissected and snap-frozen in liquid nitrogen and stored at − 80 °C until RNA extraction. Total RNA was extracted using TRIzol reagent (Invitrogen, Carlsbad, CA), and the mRNA purified with RNeasy Mini Kit (Qiagen, Venlo, The Netherlands) with 1% β-mercapto ethanol and treated with DNAse. The mRNA integrity was checked on an Agilent 2100 Bioanalyzer (Agilent Technologies, Amsterdam, The Netherlands) (average RIN 9.2), and individual RNA samples (4 μg per animal) were labelled and hybridised on a Affymetrix NuGO mouse array as described previously .
In situ hybridisation
The riboprobe for serpinA3N, accession no. BC013651, was derived using the forward primer 5′CTACGCGGGCAAGAGGA3′ and the reverse primer 5′AAGGGGGCAATTTCAGTTT3′. The size of the amplified insert was 543 bp. Automated sequencing was performed to verify the probe sequence.
Messenger RNA levels were quantified by in situ hybridisation, on 20-μm thick coronal hypothalamic cryo-sections, using techniques described in detail elsewhere . Briefly, slides were fixed in 4% (w/v) paraformaldehyde in 0.1 mol/l PBS for 20 min at room temperature, washed in PBS, incubated in 0.1 mmol/l triethanolamine for 2 min and acetylated in 0.1 mmol/l triethanolamine and 0.25% (v/v) acetic anhydride for 10 min. Sections were dehydrated in ethanol and dried under vacuum before hybridisation with riboprobes at 106 cpm/ml for 18 h at 58 °C. After hybridisation, sections were desalted through a series of washes in standard saline citrate (SSC) to a final stringency of 0.1× SSC at 60 °C for 30 min, treated with RNase A and dehydrated in ethanol. Slides were apposed to Biomax MR (Sigma-Aldrich, UK) together with [14C] micro-scale standards (Amersham International, Amersham, UK) at room temperature for varying lengths of time depending on the probes used to ensure that the optical density of areas to be measured fall within the linear region of the standard curve.
Autoradiographs were scanned on a Umax Power Look II (UMAX Data Systems, Fremont, CA, USA). Integrated optical densities (IOD) of specific nuclei were quantified with reference to a mouse brain atlas  using the Image Pro-plus system (Media Cybernetics, Silver Springs, MD, USA). IOD was converted to nCi/g using [14C] microscale standard curves for measures of total gene expression.
Frozen sections (20 μm) were first incubated with goat anti-mouse serpinA3N (R&D Systems cat. no. AF4709) at a dilution of 1:1000 overnight at 4 °C then incubated for 30 min at room temperature with biotinylated anti-goat IgG (Vector Labs cat. no. PK-6105) according to the manufacturer’s instructions followed by ABC reagent (Vector Labs cat. no. PK-6105) and stained with 3,3′-diaminobenzidine (DAB) substrate solution (brown) (Vector Labs cat. no. SK-4100). Sections were then thoroughly washed and incubated with either chicken anti-GFAP (Millipore, UK cat. no. AB5541), rabbit anti-IbA1 (Wako cat. no. 019-19741), rabbit anti-NPY (ThermoFisher Scientific cat. no. PA5-19568) or rabbit anti-AgRP (Phoenix Pharmaceuticals cat. no. H-003-57) at a dilution of 1:300 overnight at 4 °C and then at room temperature for 30 min with either goat anti-chicken IgG (Vector Labs cat. no. BA-9010) at a dilution of 1:200 followed by Vectastain Elite ABC kit (goat IgG) (Vector Labs cat. no. PK-6105) or directly with the Vectastain Elite ABC kit (goat IgG) and stained with Vector SG (blue) (Vector Labs cat. no. SK-4700). Control sections omitted the primary antibodies.
Neuronal culture and reagents
To investigate the regulation of serpinA3N gene expression specifically in neurons, the embryonic immortalised hypothalamic cell line, N42, was used (Cellution Biosystems Inc., Ontario, Canada. Please see https://www.cedarlanelabs.com/Products/Detail/CLU122 for a comprehensive list of all genes expressed by these cells including the leptin receptor). These cells have been previously shown to provide a good model for hypothalamic neuron gene expression studies .
Cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies, Paisley, UK) supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin (Life Technologies) maintained at 37 °C under 5% CO2. Neurons were grown in 60-mm plates (n = 6) to 90% confluence then challenged with either 50 nM leptin (R&D Systems, Abingdon, UK), 200 μM palmitic acid or 200 μM oleic acid conjugated to fatty acid-free bovine serum albumin (BSA) (Sigma-Aldrich, UK), or the appropriate vehicle as a control. For leptin, this was a mixture of 12 μM HCl and 6 μM NaOH and for fatty acids 50 μM fatty acid-free BSA. To inhibit the NFkB pathway, N42 neurons were treated with 50 μM BSA or 200 μM palmitate in the presence and absence of 25 μM of the NFkB inhibitor BAY 11-7082 (Cayman Chemical, UK). All solutions were filter sterilised prior to use. For all treatments, medium was removed after 6 h.
After the challenge, the medium was removed and cells were lysed using RLT lysis buffer (RNeasy Mini Kit Qiagen, Venlo, The Netherlands). Cell lysates were then collected and RNA extracted using an RNeasy Mini Kit (Qiagen) following the manufacturer’s instructions. RNA integrity was assessed by an Agilent 2100 Bioanalyzer (Agilent Technologies, Amsterdam, The Netherlands). One microgram of total RNA was reverse transcribed to generate cDNA using Superscript II reverse transcriptase (Life Technologies, CA, USA). Real-time PCR was carried out using Taqman Fast Universal PCR master mix (Applied Biosystems, USA) according to manufacturer’s instructions using the following Taqman assays: B2M (Mm00437762_m1), serpinA3N (Mm00776439_m1), IL-6 (Mm00446190_m1) and TNFα (Mm00443258_m1). Each reaction used 1 μL of cDNA template.
N42 neurons were grown as described earlier. The cell culture medium was collected and protein concentrated using an Amicon Ultra-0.5 Centrifugal Filter (10 K device, Millipore, UK). For lysate preparation, cells were scraped into 1 ml of PBS and pelleted by centrifugation; 1 ml of M-PER mammalian protein extraction reagent (Thermo scientific) was added to the cell pellet before sonication using a Sanyo Soniprep 1500 to ensure complete cell lysis. Protein concentrations were determined using the Pierce 660 nm protein assay reagent (Thermo Scientific). Samples were then diluted 3:1 with 4× Laemmli sample buffer (Bio-Rad, UK) with 2-mercaptoethanol (9:1 ratio) and boiled for 10 min, and 2 μg of protein was loaded on the gels. For media in which no cells were cultured, used as a control, an amount equivalent to 5 μL of concentrated media was loaded and as a positive control 12.5 ng of recombinant mouse serpin α1AC protein (R&D Systems). Proteins were separated on 10% mini-PROTEANTGX Precast Gels (Bio-Rad) and transferred to a PVDF Membrane (Bio-Rad) before immuno-detection using goat anti-mouse serpinA3N (R&D Systems) and peroxidase-linked secondary antibody (Donkey polyclonal antibody to goat IgG (HRP), abcam, UK). Chemiluminescent signal on the blots was detected using a Fujifilm LAS-3000 Imager after incubation with Clarity Western ECL substrate kit (Bio-Rad) using the manufacturer’s recommended protocol. Additional gels were run in parallel and stained with Colloidal Coomassie Blue (Safe Stain) (Severn Biotech Ltd) in order to visualise total protein present in cell media and lysates.
Data are presented as mean ± SEM and were analysed using GenStat (GenStat, Eighth Edition (2005), VSN International Ltd., Oxford). In the case of experiments testing the influence of a single factor, a one-way ANOVA was performed. Where two or three factors were compared in a single experiment, a two- or three-way ANOVA followed by post hoc Student’s t tests based on the LSD were performed. In this case, the ANOVA results are expressed in the figure legend and the results of the Student t test are represented on the graph. P < 0.05 was considered statistically significant.
Analysis of variance
Bovine serum albumin
Cocaine- and amphetamine-regulated transcript
- db/db :
Diabetic obese mice with a spontaneous non-functional mutation in the leptin receptor
Dulbecco’s modified Eagle’s medium
Dorsomedial nuclei of the hypothalamus
Glial fibrillary acidic protein
Ionised calcium binding adaptor molecule 1
Inhibitor of nuclear factor kappa-B kinase subunit β
- IL-1R1 −/− :
Interleukin-1 receptor knockout mice
Integrated optical density
c-Jun amino-terminal kinase
Least significant difference
mHypoE-N42 hypothalamic neuronal cell line
Nuclear factor kappa-light-chain-enhancer of activated B cells
- ob/ob :
Obese mice with a spontaneous mutation in the gene which produces leptin
Standard error of the mean
Standard saline citrate
Toll-like receptor 4
- TNFα :
Tumor necrosis factor alpha
University College Dublin
Ventromedial nuclei of the hypothalamus
World Health Organisation. Obesity and overweight. Fact sheet No311. 2014.
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LMW, CG, ACM, EB, AM, BdR, MVB, MM and C-DM were supported by a project grant from NuGO; LMW, AM and FHM were supported by a project support grant from the British Society for Neuroendocrinology; DS was supported by a SULSA studentship; FHM was supported by a EASTBIO DTP BBSRC studentship; LMW, CG, ACM, EB, BdR, C-DM, FMC, PN, JED and NH were funded by the Scottish Government’s Rural and Environment Science and Analytical Services Division (RESAS).
AT and KC were funded by the German Ministry of Research and Education (Ref. No: 0315087).
HMR was supported by the Irish Department of Agriculture, Food and Marine ImmunoMet Programme (14/F/828). FCM and HMR were supported by Science Foundation Ireland Principal Investigator Programme (11/PI/1119).
RN and CD were supported by grants from Ministerio de Economia y Competitividad (CD: BFU2011-29102; RN: BFU2012-35255), Xunta de Galicia (RN: EM 2012/039 and 2012-CP069). Centro de Investigación Biomédica en Red (CIBER) de Fisiopatología de la Obesidad y Nutrición (CIBERobn). CIBERobn is an initiative of the Instituto de Salud Carlos III (ISCIII) of Spain which is supported by FEDER funds. The research leading to these results has also received funding from the European Community’s Seventh Framework Programme under the following grants: no 245009: NeuroFAST to CD and ERC StG-2011-OBESITY53-281408 to RN.
Availability of data and materials
The transcriptomic data discussed in this publication have been deposited in NCBI’s Gene Expression Omnibus  and are accessible through GEO Series accession number GSE113943 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE113943) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi).
The authors declare that they have no competing interests.
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