Article Text


Leptin secretion and leptin receptor in the human stomach


BACKGROUND AND AIM The circulating peptide leptin produced by fat cells acts on central receptors to control food intake and body weight homeostasis. Contrary to initial reports, leptin expression has also been detected in the human placenta, muscles, and recently, in rat gastric chief cells. Here we investigate the possible presence of leptin and leptin receptor in the human stomach.

METHODS Leptin and leptin receptor expression were assessed by immunohistochemistry, reverse transcriptase-polymerase chain reaction (RT-PCR), and western blot analysis on biopsy samples from 24 normal individuals. Fourteen (10 healthy volunteers and four patients with non-ulcer dyspepsia and normal gastric mucosa histology) were analysed for gastric secretions. Plasma and fundic mucosa leptin content was determined by radioimmunoassay.

RESULTS In fundic biopsies from normal individuals, immunoreactive leptin cells were found in the lower half of the fundic glands. mRNA encoding ob protein was detected in the corpus of the human stomach. The amount of fundic leptin was 10.4 (3.7) ng leptin/g mucosa, as determined by radioimmunoassay. Intravenous infusions of pentagastrin or secretin caused an increase in circulating leptin levels and leptin release into the gastric juice. The leptin receptor was present in the basolateral membranes of fundic and antral gastric cells. mRNA encoding Ob-RL was detected in both the corpus and antrum, consistent with a protein of ∼120 kDa detected by immunoblotting.

CONCLUSION These data provide the first evidence of the presence of leptin and leptin receptor proteins in the human stomach and suggest that gastric epithelial cells may be direct targets for leptin. Therefore, we conclude that leptin may have a physiological role in the human stomach, although much work is required to establish this.

  • leptin
  • leptin receptor
  • human stomach
  • gastrin
  • secretin

Statistics from

Leptin, the product of the obgene,1 is an adipocyte hormone which regulates energy homeostasis by informing the brain about fatty tissue mass.2-4 Injection of exogenous leptin intoob/ob mice inhibits food intake and reduces body weight via activation of specific brain receptors.5 6 Conversely, leptin deficiency in mice and humans causes obesity and may also cause diabetes syndromes, including hyperinsulinaemia.7 8 Recent reports have shown that leptin inhibits insulin secretion9 10 and stimulates glucose transport and turnover in hepatocytes.11 12Contrary to initial reports, leptin is not restricted to adipocytes. It has also been detected in the human placenta,13muscles,14 and rat gastric chief cells.15Detection of leptin in rat gastric epithelium prompted us to investigate the possible presence and role of leptin and its receptors in the human stomach.

Materials and methods


For immunocytochemical studies, 24 individuals were randomly selected from the files of our gastroenterology department (Bichat Hospital, Paris, France), these cases having been reported elsewhere.16 17 They included 15 healthy volunteers and nine patients with non-ulcer dyspepsia (n=24) who gave informed consent for upper endoscopy and gastric secretory tests.

Secretory studies available for 14 (10 healthy volunteers and four with non-ulcer dyspepsia) of the 24 subjects (mean age 45 years; range 24–60; five women, nine men) were analysed. At the time of the study all had normal endoscopy and normal gastric mucosa on histological examination. None was receiving antisecretory drugs and other drug treatments were stopped 48 hours before the secretion tests.


Biopsies were performed during endoscopic examination. At least four samples were collected from antral and fundic sites. Samples were fixed in Bouin's solution or buffered formalin for 24 hours, dehydrated, and embedded in paraffin. Sections (4 μm) were stained with haematoxylin-eosin-Safran to assess if the normal gastric mucosa was well oriented, and immunohistochemical staining was performed using the avidin biotin complex, diluted 1:100 (Kit ABC Vectastain; Vector Laboratories Burlington, California, USA), and diaminobenzidine to detect peroxidase activity. The antibodies used were: (a) a polyclonal antibody raised in rabbits against the carboxyl terminal fragment (137–156) of mouse leptin (A-20) and (b) a polyclonal antibody raised in goats against the C terminal fragment (1146–1165) of human leptin receptor (C-20) (Santa Cruz Biotechnology, California, USA). For leptin immunostaining, antileptin antibody was diluted 1:50 and sections were incubated for one hour at 37°C using a microwave method. For leptin receptor, antireceptor antibody was used at a dilution of 1:25 or 1:50 on tissue previously digested with 0.1% pepsin in 0.01 N HCl, pH 2.25, for eight minutes at room temperature to retrieve antigen. Then, incubation was performed overnight at 4°C. For controls, no immunostaining was observed in gastric tissues under the following conditions: (a) omission of the primary antibody, (b) for leptin receptor only, normal goat serum used in place of immune goat serum; (c) overnight prior incubation of the antileptin antibody with 40 μg of the homologous peptide per ml of diluted antiserum at 4°C; and (d) prior incubation of antireceptor antibody with 40 μg of homologous peptide per ml of diluted antiserum for 3–4 hours at room temperature.

Sections of fatty tissues were fixed in the same way and were used as positive controls for leptin immunostaining.


After an overnight fast, gastric juices were collected using a nasogastric tube as previously described.16 17 The stomach was first emptied for 15 minutes and then basal gastric juice was collected by gentle manual suction every 15 minutes for one hour. Pentagastrin (6 μg/kg/h) or secretin (3 IU/kg/h) was infused for one hour. Gastric juices and blood samples were collected every 15 minutes for determination of leptin. The volume of gastric juice was measured and the acid concentration was determined by titration. Mean integrated basal acid output and stimulated acid output in millimoles of [H+] per hour were calculated as the sum of the four 15 minute samples. The 15 minute samples were stored at −20°C until leptin assay by radioimmunoassay (RIA).


125I labelled human leptin (∼6×104cpm; Linco Research Inc, St Charles, Missouri, USA) was incubated with or without stimulated gastric juice (pH 1.8) for 30 minutes at 37°C and eluted at room temperature from a Sephadex G-100 gel filtration column with 25 mM phosphate buffered saline, pH 7.4, containing 0.01% sodium azide. Fractions (1 ml) were collected and the radioactivity of each sample was determined. The total amount of radioactivity eluted in the peak was calculated and per cent recovery determined.


Leptin was measured on fundic biopsy samples from five of the 14 individuals who underwent the secretion tests. Biopsy samples were weighed and homogenised in Krebs-Ringer-HEPES (1 mg wet weight per millilitre) with a glass Teflon homogeniser. The homogenates were centrifuged at 10 000 g for 10 minutes. The supernatants were used for leptin assays. Fundic, plasma, and gastric juice leptin contents were estimated using a human leptin RIA kit from Linco Research Inc.


Reverse transcription-polymerase chain reaction (RT-PCR) was performed with total RNA extracted using Trizol reagent (Gibco BRL, France) from human fundic biopsy samples. Firstly, strand cDNA was prepared from 4 μg of total RNA according to the manufacturer's procedure (Pharmacia Biotech, Saclay, Orsay, France) using murine reverse transcriptase. It was amplified by PCR using primers based on the human oband Ob-RL genes. The cDNA primers for the ob gene were1: f5′-CCTGACCTTATCCAAG ATGG-3′ and r5′-GAGTAGCCTGAAGC TTCCAG-3′, and for the Ob-Rb gene18 (huB219.1), f5′-GCCAACAACTGTGGTC TCTC-3′ and r5′-AGAGAAGCACTTGG TGACTG-3′. The sample was denatured at 95°C for three minutes. PCR was carried out for 40 cycles of one minute denaturation at 95°C, 30 seconds annealing at 62°C, and two minutes of extension at 72°C. Amplification was terminated by a final 10 minute extension step at 72°C. In controls, RT was omitted to demonstrate that PCR amplification was not due to contamination with genomic DNA. Electrophoresis in a 1% agarose gel and ethidium bromide staining were used to verify the PCR products. The expected 224 bp and 246 bp were detected for the ob gene and for Ob-Rb, respectively.


Samples from fundic and antral biopsies, and from the entire rat brain (positive control) were weighed and immediately frozen in liquid nitrogen and stored at −80°C. They were homogenised at 4°C in RIPA buffer containing 0.1 mg/ml PMSF, 100 μM benzamidine, and 100 mM Na3VO4 as protease inhibitors. They were resolved on 7.5% SDS-PAGE gel electrophoresis after loading 20–40 μg of total protein. Protein bands were transferred to nitrocellulose sheets and probed with polyclonal antileptin receptor antibody C-20 or K-20 (Santa Cruz Biotechnology). The specificity of the immunoreactive bands was verified by preincubating the antibodies overnight with 40 μg of their homologous peptide. The immune complex was revealed by an enhanced chemiluminescence detection system (Amersham, France).


A gastrin RIA (Gammadab, New York, USA) with a polyclonal antibody directed against the COOH terminal fragment of G-17 and G-34 was used. Serum gastrin levels were determined before and one hour after the pentagastrin or secretin infusion tests.


Results are expressed as mean (SEM) or median (range) for individuals, or the mean value in each test period was used for statistical comparisons. Acid and leptin secretions under basal conditions were compared with those during pentagastrin and secretin stimulation using the Mann-Whitney U test with significance at p<0.05.



In all specimens of normal human gastric mucosa, leptin immunoreactive cells were detected in the fundic epithelium. They were concentrated in the lower half of the glands at a site similar to that of chief cells, as shown in rats (fig 1A). Leptin immunostaining was also strong in the canaliculi of the parietal cells (fig 1B). The staining was leptin specific as it disappeared if the antibody was adsorbed onto the antigen fragment before use (fig 1C). No leptin immunoreactive cells were detected in the antrum (not shown). RIA determinations for fundic biopsies showed a mean of 10.4 (3.7) ng leptin/g mucosa for five subjects (table 1).

Figure 1

Leptin immunostaining in normal human fundic mucosa (Bouin's fixed, paraffin embedded tissue sections). (A) Leptin immunoreactive cells are present in the lower half of the fundic epithelial glands. (B) High magnification of leptin containing cells: leptin immunostaining was visible in the canaliculi of the parietal cells (arrows). (C) Serial section of the same region: no immunoreactivity after adsorption of the antiserum with 40 μg/ml of leptin fragment (137–156).

Table 1

Characteristics of the 14 healthy individuals in the gastric secretion studies


Leptin was detected in gastric juice at basal concentrations of 0.2–0.6 ng/ml (mean 0.3 (0.04) ng/ml). Basal leptin output was 25.2 (5.2) ng/h (table 1). Secretin infusion increased circulating plasma leptin levels by 28%, which paralleled the increase in leptin output in gastric juice, reaching a mean value of 1165.8 (130.1) ng/h. Intravenous infusion of pentagastrin also significantly increased leptin output in gastric juice to a mean of 91.7 (14.3) ng/h (fig 2A). This was accompanied by a 25% increase in circulating plasma leptin (1.8 (0.5) v 2.4 (0.3) ng/ml; p<0.05). The secretin induced increase in leptin output in gastric juice was markedly higher than that induced by pentagastrin infusion (1165.8 (130.1) v 91.7 (14.3) ng/h; p<0.001) (fig 2B). Secretin inhibited acid secretion but circulating gastrin levels were unaffected (data not shown).

Figure 2

Effect of secretin on leptin secretion into the gastric juice and blood (A), and individual integrated gastric leptin outputs (B) after pentagastrin or secretin infusion in humans. The solid line represents the median value in each group. Median (range) values are: control 18.8 (10.7–61.2) ng/h; pentagastrin 107 (39–150) ng/h; and secretin 1009 (940–1640) ng/h.


Figure 3 shows a representative elution profile for Sephadex G-100 gel filtration of 125I leptin incubated for 30 minutes with or without stimulated gastric juice (pH 1.8). 125I labelled human leptin eluted in one peak and showed no apparent dissociation because 80% was recovered from gel filtration. Leptin was incubated with gastric juice and subjected to gel filtration. One peak was eluted in the bed volume suggesting that leptin was not associated with macromolecules or proteolytically degraded.

Figure 3

Sephadex G-100 elution profiles after incubation of125I labelled human leptin with or without pentagastrin stimulated gastric juice (pH 1.8) for 30 minutes at 37°C. A typical experiment is shown; the three experiments performed show a single peak under both sets of conditions.


Leptin receptors were detected in fundic and antral epithelial cells (fig 4). Staining was more intense in superficial and pit cells than in glandular cells. It was restricted to the basolateral membrane and, in the fundic mucosa, to parietal cells, with a stronger signal on sections of the microcanaliculi in some but not all parietal cells. Prior immunoadsorption of the antibody with the corresponding antigen resulted in a reduction in or total abolition of immunostaining of the membrane and parietal cells, except for the microcanaliculi where it was only slightly decreased. However, there was no staining if the primary antibody was omitted, and very weak diffuse background staining throughout the tissue with no particular staining of the microcanaliculi if the corresponding normal serum was used rather than primary antiserum.

Figure 4

Leptin receptor immunostaining in normal human gastric mucosa. Tissues sections were fixed in Bouin's solution and embedded in paraffin. Nuclei were counterstained with Mayer's haemalum. (A) Fundic mucosa and (C) antral mucosa. Immunostaining was detected in superficial and pit epithelial mucous cells in the two mucosae and in fundic parietal cells; (B) and (D) are adjacent sections. The signal is much weaker and even absent if the antibody is adsorbed with the antigen. (E) Detail of immunostaining located on the lateral and particularly the basal (arrows) membranes in superficial and crypt mucous cells. (F) Detail of parietal cells; a strong signal is visible in sections of microcanaliculi.


Finally, mRNA encoding ob protein was detected only in the corpus while mRNA encoding Ob-RL was detected both in the corpus and antrum of the human stomach (fig 5A). Western blot analysis of total protein with two independent antibodies for leptin receptor showed an immunoreactive band with a predicted size of ∼120 kDa in the corpus and antrum (fig 5B).

Figure 5

Leptin and leptin receptor expression in the human stomach. (A) Reverse transcription-polymerase chain reaction (RT-PCR) analysis of mRNA: lane 1, marker ladders; lane 2, leptin mRNA in fundic epithelium; lane 3, leptin receptor mRNA; lane 4, reverse transcriptase omission. Expected sizes for PCR products: 224 bp for leptin and 246 bp for human leptin receptor. (B) Western blot of leptin receptor with antibodies K-20 and C-20 in fundic (F) and antral (A) extracted total proteins from human gastric biopsies and from rat brain (Br) as a positive control. A representative immunoblot with antibody K-20 is shown. One leptin receptor immunoreactive band with a molecular size of about 120 kDa was detected.


We have shown that leptin and its receptor are present in the human gastric mucosa and provide the first evidence that leptin is a stomach derived protein in humans. In addition, leptin mRNA was found and leptin containing cells were restricted to the lower half of the fundic glands at a site similar to that of the pepsinogen secreting chief cells, as previously found in rats.15 In contrast with the results obtained in rat gastric mucosa, we detected additional immunoreactivity on the parietal cell canaliculi that was abolished by immunoadsorption. This suggests simple accumulation of luminally secreted leptin in the acidic compartment of the parietal cell or alternatively, binding of leptin to receptors on parietal cell microcanaliculi.

The amount of gastric leptin determined by RIA was twice that reported for rats. Gastric leptin is simultaneously released into the blood and gastric juice by pentagastrin and secretin. These data are consistent with results in rats showing that cholecystokinin (CCK) causes a significant decrease in fundic leptin content. Secretin stimulation of gastric leptin output is not dependent on gastric acid secretion. Indeed, secretin inhibited acid secretion consistently in previous reports in rats,19 dogs,20 and humans21 but had no effect on circulating gastrin levels. Thus this effect is probably a direct effect of secretin on gastric chief cells, consistent with the presence of secretin receptors on these cells and the efficacy of secretin for stimulating pepsinogen secretion.22 23

The leptin receptor was detected on the basolateral membranes of epithelial fundic and antral cells. However, an additional signal was detected on sections of the parietal cell canaliculi in the fundic mucosa. The reason for this is unclear. Prior immunoadsorption of the antibody with the corresponding antigen abolished basolateral staining thereby supporting its specificity. Staining of parietal cell canaliculi was not completely abolished by antigen adsorption, even if other controls were negative. Therefore, whether the leptin receptor is really present on the apical membrane invagination of the parietal cells requires further investigation.

Several isoforms of the leptin receptor generated by alternative mRNA splicing have been previously reported.5 6 One short form was detected in almost all tissues whereas the longest form, Ob-Rb, was found to be highly expressed in the hypothalamus6 and also in some peripheral tissues.18 24 25 26 In this study, a protein of approximately 120 kDa was detected by immunoblotting in both the normal corpus and antral gastric mucosa of humans. This protein is the same size as the ∼120 kDa protein detected in pancreatic islets transfected with Ob-Rb cDNA to overproduce wild-type Ob-Rb.27 It is also consistent with previous studies showing that there are multiple mRNA splicing variants for the leptin receptor in the stomach.28 In total, our findings clearly support the conclusion that human stomach expresses the longest form of the leptin receptor (Ob-Rb).

It is thought that only the Ob-Rb receptor, which contains the box1 and box3 motifs, activates the JAK/STAT cascade, mediating the biological effects of leptin.29-32 Therefore, our findings suggest that human gastric epithelial cells are direct targets for gastric leptin. It is not known if activation of these putative targets involves luminal, endocrine, or paracrine pathways. However, the presence of the receptors on the basolateral side suggests an endocrine and/or paracrine pathway but further investigations are required to resolve this issue.

In terms of physiological function, gastric leptin may be involved in the short term control of satiety, acting in synergy with CCK via vagal afferent fibres in rat.33 Demonstration in this study that leptin receptors are present on gastric epithelial cells in humans suggests that leptin may have an additional action on these cells which are responsible for control of their secretory function. Alternatively, leptin secreted into the gastric juice, if not degraded, may reach the intestine, having biological effects on food digestion and absorption, as recently suggested by the effects of leptin on intestinal cells.34

In summary, we have demonstrated that in the human stomach, leptin is produced by the pepsinogen secreting chief cells of the fundic mucosa. We have also provided evidence that gastric epithelial cells bear the functional leptin receptor. Thus gastric epithelial cells may be physiological targets for gastric leptin. Our findings may open a new field of investigations into the actions of leptin.


We thank Michel Saadoun and Isabelle Prevost for technical support.


View Abstract


  • Abbreviations used in this paper:
    reverse transcription-polymerase chain reaction

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