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MS 9535 Received 21 April 1999; accepted after revision 19 May 1999
The interior face of the stomach is lined by one of the most highly organized populations of epithelial cells in the body. These cells are responsible for the secretion of acid, pepsinogen and mucus into the lumen. Epithelial function is regulated by systems that match secretion to the presence of food in the lumen, that control the expression of genes associated with secretory function, and that determine the renewal of cells and the proportions of different cell types. In recent years the application of molecular cell physiological approaches, including transgenesis, has shed new light on the relevant endocrine and paracrine control systems. This review focuses on recent progress in understanding how endocrine cell signals, and in particular the gastrins, influence the organization and function of the acid-secreting epithelium.
Architecture of the corpus mucosa
The gastric epithelium is folded into glands, which are the distinctive feature of the gastric mucosa. In the body or corpus of the stomach, the major differentiated glandular cell types are parietal (or oxyntic) cells secreting HCl, zymogen (chief or peptic) cells secreting pepsinogen, and surface epithelial/mucus neck cells secreting mucus glycoprotein. Intrinsic factor is secreted by parietal cells in man, and by chief cells in mouse. The corpus epithelium also contains endocrine cells that regulate acid secretion through paracrine mechanisms, the most important being histamine-releasing enterochromaffin-like (ECL) cells and somatostatin-releasing D-cells. In the glands of the pyloric antral part of the stomach, parietal and ECL cells are absent, but there is an additional endocrine cell type - the gastrin (G) cell (Walsh, 1994). In the proximal stomach of some species, e.g. the rat, there is squamous (or non-glandular) epithelium, which is not considered here.
A single multipotent class of stem cell gives rise to the various differentiated cell types of the epithelium. Proliferative cells are located in the isthmus region of the gland. Some cells migrate upwards, becoming mucus-secreting surface epithelial cells and surviving 2-3 days; other cells within the proliferative zone differentiate into parietal, chief or ECL cells and subpopulations migrate towards the base of the gland, surviving 50-190 days. The proliferation and differentiation of epithelial cells are determined partly by interactions between different cell types (Karam, 1995). Mature parietal cells, in particular, seem to determine the fate of other epithelial cells. For example, parietal cells have been selectively lesioned in transgenic mice by using the promoter of the H+,K+-ATPase 
-subunit gene to direct expression to parietal cells of toxic agents such as diphtheria toxin, and herpes virus thymidine kinase - which generates a toxic product on treatment with the drug ganciclovir (Li et al. 1996; Canfield et al. 1996). The loss of parietal cells in these animals is also associated with loss of chief cells, even though the transgene is not expressed in zymogen cells, indicating interactions between these cells in determining their differentiation. In addition to these interactions, however, it is also clear that the pyloric antral hormone gastrin regulates not just acid secretion, but also the proliferation of gastric epithelial cells (Johnson, 1988; Ohning et al. 1996) and the relative numbers of different cell populations in the epithelium, thereby influencing secretory capacities (Koh et al. 1997; Friis-Hansen et al. 1998).
Antral-corpus interactions control acid secretion
The events leading to increased gastric acid secretion during digestion are initiated by cephalic stimuli that activate vagal efferent pathways. Thereafter, food in the stomach maintains acid secretion by activating both neural (local and vago-vagal) and endocrine reflexes. The endocrine systems of the corpus and antrum contribute in separate ways. Gastrin is the major output of the antral endocrine cell system and is a major stimulant of acid secretion. The G- and D-cells of the pyloric antral mucosa act in concert as transepithelial transducers monitoring luminal nutrients (protein and amino acids) and pH, respectively. Somatostatin is secreted from antral D-cells when luminal pH falls below 3·5; it acts by a paracrine mechanism to suppress G-cell function, thereby completing a negative feedback loop controlling acid secretion. A reduction in acid secretion, for example following the administration of proton pump inhibitors such as omeprazole, inhibits D-cells and so upregulates G-cells (Brand et al. 1988; Wu et al. 1990; Dimaline et al. 1991).
The two main endocrine cell types of the corpus differ from antral endocrine cells in that they seem not to respond directly to luminal chemicals. Instead, they act as integrators of neurohumoral signals. Thus gastrin releases histamine from ECL cells, which in turn increases acid secretion by acting at parietal cell histamine-H2 receptors. Both parietal and ECL cells are inhibited by somatostatin released from corpus D-cells in response to a variety of neurohumoral agents, e.g. noradrenaline, vasoactive intestinal polypeptide (VIP), calcitonin gene-related peptide (CGRP) and cholecystokinin (CCK). The somatostatin receptor type 2 (SSTR2) is important in mediating these effects, since mice in which the SSTR2 gene has been deleted exhibit increased basal and stimulated acid secretion (Martinez et al. 1998).
Multiple gastrins and receptors
It used to be thought that the main active forms of gastrin were the COOH-terminally amidated gastrins of 34 and 17 amino acid residues (G34 and G17) first characterized over 25 years ago (Gregory & Tracy, 1964, 1972). Recent studies indicate that this is an oversimplification: there is an unexpected variety both in the identity of the active products generated from the gastrin precursor during biosynthesis, and in the responses to these peptides (Fig. 1A and B).
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A, schematic of the main products of preprogastrin processing. The signal sequence (green) of preprogastrin is cleaved in the endoplasmic reticulum and progastrin then passes through the Golgi complex to secretory vesicles where it is cleaved (dashed arrows) and the COOH-terminus amidated; processing enzymes are indicated in the boxes. B, the pathways of post-translational processing of rat preprogastrin as revealed by pulse-chase kinetic studies are shown together with a summary of the main biological properties of the various progastrin-derived peptides. C, putative mechanisms regulating progastrin processing are shown: selected cleavages are inhibited by raising intravesicular pH and by phosphorylation by physiological casein kinase. The inset shows the primary sequence of the cleavage/phosphorylation site in the single-letter notation. Cleavage sites (Arg57,58, Lys74,75, Arg94,95) are also identified in the single-letter notation. | ||
The gastrin family of peptides
The rate of clearance of G17 from the circulation is about five times that of G34 (Walsh et al. 1974). The release of G34 therefore leads to changes in plasma concentrations that are higher and more persistent compared with the secretion of equimolar amounts of G17. The COOH-terminal amide moiety of these peptides has long been thought to be essential for the stimulation of acid secretion and cell proliferation (Johnson, 1988; Walsh, 1994). This view has now been revised and extended with the observation that gastrins with COOH-terminal glycine (G-Gly), and intact progastrin, also stimulate proliferation (Seva et al. 1994; Wang et al. 1996; Koh et al. 1999). In addition, G-Gly increases expression of the parietal cell proton pump gene (Todisco et al. 1995), but neither G-Gly nor progastrin is an acid secretagogue on its own. Because G-Gly and progastrin are biosynthetic precursors of the amidated peptides, the control of progastrin processing allows the production of multiple, alternative, active products from a single precursor molecule (Dockray et al. 1996) (Fig. 1B).
Gastrin biosynthesis
Experiments using pulse-chase labelling protocols show that like other peptide hormones, the gastrin precursor, preprogastrin is translated at the endoplasmic reticulum (ER) where the signal peptide is rapidly removed (Varro & Dockray, 1993). Progastrin then progresses through the Golgi complex. In the trans-Golgi network (TGN), tyrosine-86 may be sulphated and serine-96 may be phosphorylated (Varro et al. 1994). The cleavage of progastrin at two pairs of Arg residues (positions 57 and 58, and 94 and 95) occurs relatively rapidly after exit from the TGN (t½ 
10 min) to secretory vesicles (Varro et al. 1995); further cleavage at a pair of Lys residues (positions 74 and 75) occurs more slowly (t½ 60 min). These cleavages are thought to be mediated by the prohormone convertases PC1/3 and PC2 (Macro et al. 1997) (Fig. 1A). The cleavage products terminate in a pair of COOH-terminal basic residues that are removed by carboxypeptidase E (CPE). A mis-sense mutation in the CPE gene in Cpefat/Cpefat mice leads to substantially reduced tissue concentrations of the amidated gastrins and an accumulation of processing intermediates terminating in -Arg-Arg (Udupi et al. 1997).
The products of proteolysis in G-cells are peptides of 18 and 35 residues with a COOH-terminal Gly residue (i.e. G17-Gly and G34-Gly). The COOH-terminal Gly-gastrins are converted to amidated gastrins by the action of the bifunctional enzyme peptidyl 
-amidating mono-oxygenase (PAM). The mono-oxygenase domain of PAM first converts the Gly residue to Gly-OH in a reaction requiring copper, ascorbate and molecular oxygen (Fig. 2). This intermediate is then converted by the lyase domain of PAM to the corresponding COOH-terminal amide (Eipper et al. 1993). In rat G-cells, amidation continues up to about 80 min after the arrival of progastrin in secretory vesicles and then stops, even though about 50 % of the substrate remains unconverted at this time (Varro et al. 1995). Kinetic studies suggest that in the rat the major intermediate, G34-Gly, is either converted via G34-GlyOH to G34, or alternatively cleaved to G17-Gly (Fig. 1B). The amidated peptide G34 may in turn be cleaved to G17, but the evidence suggests that G17-Gly is not normally converted to G17 (Varro et al. 1995).
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Internal pH is approximately 5·5 due to the activity of the vacuolar proton pump (vH+-ATPase), but proton extrusion via vesicular monoamine transporters (VMAT) may raise intragranular pH and inhibit cleavage. Biogenic amines transported by VMATs are generated from their precursors by aromatic amino acid decarboxylase (AADC). The bifunctional enzyme peptidyl | ||
Modulation of progastrin processing
Because the cleavage and amidation of progastrin-derived peptides occur in vesicles of the regulatory pathway of exocytosis, there is impaired post-translational processing in cells in which these vesicles are absent. In such cells, progastrin passes directly from the TGN to the cell surface via the constitutive route of secretion (Dockray et al. 1996). This is a feature of colon cancer cells, which often express the gastrin gene (Nemeth et al. 1993; Nakata et al. 1998). Progastrin and G-Gly produced in these cells may act as autocrine growth factors, since antisense inhibition of gastrin gene expression, or gastrin immunoneutralization, inhibits cell growth (Watson et al. 1996; Singh et al. 1996).
Several different mechanisms have now been identified which determine the post-translational processing of progastrin-derived peptides in endocrine cells (Fig. 1C). (a) A proportion of progastrin is normally phosphorylated at Ser-96 (Dockray et al. 1987). Phosphorylation appears to be mediated by a TGN-resident kinase which resembles physiological casein kinase; depletion of calcium stores inhibits kinase activity, suggesting a possible mechanism to modulate prohormone phosphorylation (Fig. 1C). Site-directed mutagenesis of either Ser-96 (to Ala), or of the kinase recognition site (Glu-98 to Ala), to abolish phosphorylation, increased cleavage at Arg-94/95, so that phosphorylation of Ser-96 has inhibitory effects on subsequent cleavage (Bishop et al. 1998). (b) In antral G-cells, there is regulated expression of the genes encoding the prohormone convertases PC1/3 and PC2, which mediate progastrin cleavage. Inhibition of acid secretion with proton pump inhibitors leads to upregulation of the mRNAs encoding PC1/3 and PC2, as well as gastrin. This is associated with rapid cleavage at Lys74/75, but not at Arg57/58 or Arg94/95 (Macro et al. 1996, 1997). (c) Endocrine cell secretory vesicles are thought to have an internal pH of about 5·5, and the prohormone convertases that act in these vesicles have acidic pH optima (Fig. 1C). Raising intravesicular pH inhibits cleavage of progastrin-derived peptides at Lys-74/75, but not Arg-57/58 or Arg-94/95 (Voronina et al. 1997). G-cell secretory granules express the vesicular monoamine transporter type 1 (VMAT1), which transports biogenic amines like dopamine and serotonin into secretory vesicles in exchange for two protons, and amine loading leads to inhibition of Lys-74/75 cleavage (Hussain et al. 1999). Dietary amines such as tyramine, which are membrane permeable in their uncharged form, also inhibit G34 cleavage, although this effect is not reversed by VMAT inhibitors. Together these observations suggest that dietary and biogenic amines modulate the cleavage of progastrin-derived peptides secondary to raising intragranular pH (Figs 1C and 2).
How many receptors for gastrin-related peptides?
The amidated gastrins act at the gastrin/CCK-B receptor which is a member of the G-protein-coupled, seven transmembrane domain, receptor family. This receptor is expressed by gastric epithelial cells and by neurons in the central nervous system (Kopin et al. 1992; Wank et al. 1992a). It has similar affinities for gastrin and the structurally related brain-gut peptide, CCK; the latter is the main endogenous ligand in the CNS, and gastrin is considered to be the main peripheral ligand. In contrast, gastrins have low affinity, and CCK has high affinity, at the CCK-A receptor found on gall bladder and pancreas (Wank et al. 1992b). Activation of gastrin/CCK-B receptors increases Ca
in both ECL and parietal cells (Prinz et al. 1993, 1994; Hersey & Sachs, 1995). This is thought to be a major signalling pathway in parietal cells, but in ECL cells there is evidence that gastrin also stimulates the p42/44 MAP kinase pathway (Kinoshita et al. 1998). Unlike parietal cells, ECL cells (at least in rodents) retain the capacity to proliferate in response to gastrin, perhaps due to activation of the p42/44 MAP kinase pathway.
In addition to the gastrin/CCK-B receptor, there is evidence for at least two other putative receptors for progastrin-derived peptides. First, some colon cancer cell lines express a 78 kDa protein structurally related to fatty acid oxidation enzymes, which is reported to function as a receptor for both amidated and Gly-gastrins, but its physiological significance is uncertain (Baldwin, 1994). Second, pharmacological and binding studies in several cell lines indicate receptors that have high affinity for G-Gly (Seva et al. 1994; Singh et al. 1995; Hollande et al. 1997). The receptors in this class have not yet been cloned, and there remains some doubt as to their relative affinity for amidated gastrin. They are considered interesting, however, because they may mediate the trophic effects of progastrin derivatives in various gastrointestinal cancers.
Gastrin in genetically modified mice
The physiology of progastrin-derived peptides has recently been clarified by studies in which the gastrin gene is over-expressed in transgenic mice, or in which the gastrin (GAS-KO) or gastrin/CCK-B receptor (GAS/CCK-BR-KO) genes have been subjected to targeted deletion. In transgenic mice expressing the gastrin gene in pancreatic -cells (INS-GAS mice), the product is processed in a similar way to antral G-cells but synthesis and release are independent of the normal control mechanisms. In mice expressing the progastrin gene in the liver (H-GAS mice), the main product is intact progastrin (Wang et al. 1996). INS-GAS mice exhibit increased cell proliferation and thickness in both stomach and colon, whereas H-GAS mice exhibit increased growth of the colonic mucosa, but not of the stomach (Wang et al. 1996).
There are complementary gastric phenotypes in GAS-KO and GAS/CCK-BR-KO mice. In both cases, there are reduced numbers of parietal and ECL cells and reduced acid secretion (Nagata et al. 1996; Langhans et al. 1997; Koh et al. 1997; Friis-Hansen et al. 1998). Acid secretion in GAS-KO mice is refractory to acute administration of gastrin, acetylcholine and histamine (Friis-Hansen et al. 1998), suggesting that gastrin is required for the maturation of parietal cells. In keeping with this idea, infusion of G17 for 7 days induced acid secretion in GAS-KO mice.
It has been clear for many years that exogenous gastrin stimulates cell proliferation (Johnson, 1988). Moreover, immunoneutralization of gastrin in rats inhibits the increased gastric mucosal proliferation after feeding (Ohning et al. 1996) and, as already mentioned, the moderate hypergastrinaemia in INS-GAS mice is associated with increased gastric epithelial proliferation (Wang et al. 1996). It was therefore somewhat surprising to find that rates of gastric epithelial cell proliferation were similar in GAS-KO and wild-type mice fed ad libitum (Koh et al. 1997). There are, however, differences in the proportions of the different cell types: thus, while parietal and ECL cells are decreased in GAS-KO and GAS/CCK-BR-KO mice, the mucus-secreting neck and surface epithelial cells are increased. It seems, then, that gastrin influences cell kinetics in two ways: it is one of a variety of factors that increase proliferation, but in addition it plays a role in determining the differentiation of parietal and ECL cells from a precursor pool (Fig. 3A). Because parietal cells are terminally differentiated and do not divide, the regulatory action of gastrin in determining the numbers of these cells presumably includes events that lead to inhibition of cell division and stimulation of the expression of genes characteristic of parietal cells. Further work is now needed to define how gastrin might stimulate the proliferation of some epithelial cells while inhibiting proliferation and promoting differentiation of others.
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A, schematic representation of an acid-secreting gastric gland, showing the main classes of epithelial cell and sites of action of gastrin. Proliferation in the isthmus region followed by cell migration gives rise to mucus-secreting neck and surface cells (blue), and the main glandular cell types, i.e. parietal (green), chief (yellow) and enterochromaffin-like (ECL) cells (red). Gastrin stimulates proliferation and the differentiation of parietal and ECL cells; it also stimulates acid secretion from parietal cells, at least in part by increasing histamine synthesis and release in ECL cells. B, cellular interactions in the gastric epithelium. Gastrin stimulates histamine release from ECL cells which acts on parietal cells. Various neurohumoral agents (noradrenaline, cholecystokinin (CCK), vasoactive intestinal polypeptide (VIP) and calcitonin gene-related peptide (CGRP) stimulate somatostatin release from D-cells, which inhibits ECL and parietal cells. By an unknown mechanism, the latter also regulate chief cell numbers. C, remodelling of gastric glands with prolonged stimulation by gastrin. Hypergastrinaemia increases the expression of EGF family members such as heparin-binding EGF (HB-EGF), amphiregulin and transforming growth factor (TGF)- | ||
Enterochromaffin-like cells
Gastrin rapidly releases histamine from isolated enterochromaffin-like (ECL) cells (Prinz et al. 1993, 1994). In the perfused rat stomach, histamine secretion is decreased after 2-3 h of gastrin stimulation, presumably due to depletion of stores (Ronning et al. 1996). The maintenance of continued secretion over longer periods, and the replenishment of stores, therefore requires histamine synthesis. This is achieved by increased histidine decarboxylase activity (HDC), which converts histidine to histamine (Kahlson & Rosengren, 1971), probably secondary to regulation at both translational and transcriptional levels. Increased HDC mRNA abundance is detectable 0·5-2 h after raising plasma gastrin by refeeding in fasted rats (Dimaline & Sandvik., 1991; Dimaline et al. 1993b). Over several days, raised plasma gastrin concentrations lead to parallel increases in the abundance of mRNA species encoding HDC and vesicular monoamine transporter type 2 (VMAT2), which transports histamine from cytosol into secretory vesicles (Dimaline & Struthers, 1996), and chromogranin A (CGA), which is a major vesicle protein and a putative precursor for auto- or paracrine inhibitor peptides including pancreastatin (Dimaline et al. 1993a).
Gastrin stimulates HDC and CGA gene expression by different mechanisms. In the human gastric cancer cell line AGS-B (transfected with the gastrin/CCK-B receptor), gastrin increases expression of human HDC promoter- reporter constructs via a protein kinase C-mediated pathway acting at a novel enhancer-like response element +2 to +24 bases downstream of the transcriptional start site (Zhang et al. 1996). In contrast, stimulation of chromogranin A gene expression by gastrin in the same system is mediated by a cAMP response element (CRE) and phosphorylation of the CRE binding protein (CREB) (Hocker et al. 1998).
Gastrin and ECL cell growth
Some ECL cells are produced in the absence of gastrin, e.g. in GAS-KO and GAS/CCK-BR-KO mice, but gastrin is nevertheless an important regulator of ECL cell number. In hypergastrinaemia there is ECL cell hyperplasia and in extreme cases, the development of ECL cell carcinoid tumours (Bordi et al. 1995). Hyperplasia of ECL cells is detectable in rats within 9 days of hypergastrinaemia due to treatment with omeprazole (Tielemans et al. 1989), and is reported in patients receiving omeprazole for up to 5 years (Lamberts et al. 1993). The development of ECL cell carcinoid tumours occurs after 12-18 months in rats with hypergastrinaemia due to continuous administration of certain H2-receptor antagonists or proton pump inhibitors (Bordi et al. 1995). These tumours also occur spontaneously in the African rodent Mastomys, in which three species-specific point mutations in the gastrin/CCK-B receptor lead to its constitutive activation (Schaffer et al. 1998).
Patients with pernicious anaemia typically have hypergastrinaemia secondary to achlorhydria due to the loss of parietal cells. Approximately 5 % of these patients develop ECL cell carcinoid tumours, which often resolve after surgical resection of the antrum to lower plasma gastrin levels (Bordi et al. 1995; Higham et al. 1998). ECL cell carcinoid tumours also occur in up to 30 % of patients with hypergastrinaemia due to a gastrin-producing tumour as part of the multiple endocrine neoplasia type 1 syndrome (MEN1) (Debelenko et al. 1997). Mutations of the menin gene account for MEN1 syndrome and the protein is thought to act as a tumour suppressor; however the nature of the physiological relationship between menin and gastrin remains unclear (Chandrasekharappa et al. 1997).
A second putative tumour suppressor for ECL cell carcinoids has recently been identified; mutations of the gene encoding Reg1- have been found in several ECL cell carcinoid tumours (Higham et al. 1999). Reg1- is normally expressed in pancreas and is upregulated during differentiation of islet -cells. Recent studies indicate it is also a growth factor for gastric mucus cells (Fukui et al. 1998). In rat, it is expressed in ECL cells, in man in ECL and chief cells, and in both species its expression is increased with hypergastrinaemia (Asahara et al. 1996; Higham et al. 1999). In some ECL cell carcinoid tumours there is a mutation of the initiator methionine which disrupts the signal peptide and prevents sequestration into the secretory pathway. Together these observations are consistent with the idea that Reg1- might be an autocrine inhibitor of ECL cell growth and a stimulant of mucus cell growth, and might therefore mediate the effects of gastrin in modelling the gastric epithelium (Fig. 3C).
Parietal cell function
The question of whether gastrin stimulates acid secretion by acting directly on parietal cells or indirectly via histamine release from ECL cells (Fig. 3B) has attracted intense debate over many years (Black & Shankley, 1987). Gastrin receptors are expressed by parietal cells, gastrin modestly increases aminopyrine accumulation in isolated parietal cells (equivalent to acid secretion), and this is enhanced by histamine (Soll et al. 1984). However, quantitative pharmacological studies suggest that in the intact mucosa in vivo the predominant action of gastrin on acid secretion is secondary to histamine release (Black & Shankley, 1987). Aside from the importance of the acute effect of gastrin on parietal cells for acid secretion, the observations in GAS-KO mice cited above indicate that gastrin may act over longer periods to sensitize parietal cells to other acid secretagogues (Friis-Hansen et al. 1998).
Acid secretion and parietal cell growth and differentiation
The stimulation of acid secretion depends on the translocation into an apical canalicular system of the H+,K+-ATPase (Forte & Yao, 1996). The proton pump is subsequently retrieved into tubulovesicles on cessation of stimulation. Retrieval of the H+,K+-ATPase -subunit depends on a cytoplasmic tyrosine-based endocytosis signal. The expression in transgenic mice of a mutated version of this sequence, which inhibits retrieval, leads to chronic acid hypersecretion, the development of peptic ulcers and an increased thickness of the mucosa (Courtois-Coutry et al. 1997). Intracellular pH is controlled in part by Na+-H+ exchanger type 2 (NHE2) in the basolateral membrane. This isoform is stimulated at an extracellular alkaline pH and so is expected to be active during acid secretion when bicarbonate is released at the basolateral membrane via Cl--HCO3- exchange. In mice in which the NHE2 gene has been disrupted in exon 2, there are reduced numbers of parietal cells and zymogen cells (Schultheis et al. 1998). Thus, the homeostatic mechanisms that maintain parietal cell function during and after stimulation of acid secretion also have consequences over longer periods for maintaining parietal cell numbers and therefore epithelial organization more generally.
Corpus epithelial organization is likely to be influenced by reflex changes in G-cell function, e.g. hypergastrinaemia secondary to decreased parietal cell function, and interlinked changes in the production of soluble growth factors. Thus, gastrin stimulates the production of members of the epidermal growth factor (EGF) family, notably transforming growth factor (TGF)-, amphiregulin and heparin-binding EGF (HB-EGF) (Murayama et al. 1995; Tsutsui et al. 1997; Miyazaki et al. 1999). Overexpression of TGF- in transgenic mice produces a phenotype that resembles the human condition of Menetrier's disease, characterized by an increased growth of the gastric mucosa and an expansion of the mucus cell population of the gastric pit, but also by the inhibition of acid secretion, a decrease in mature parietal and chief cells and in the expression of the H+,K+-ATPase and pepsinogen (Takagi et al. 1992; Sharp et al. 1995). Direct evidence linking endogenous gastrin to the control of EGF-related peptides in the stomach is provided by the observation that the moderate hypergastrinaemia in INS-GAS mice initially (for the first 3 months) leads to increased acid secretion and parietal cell numbers, but in older INS-GAS mice (after 12 months) there is a progressive depression of acid secretion, loss of parietal cells, increased expression of EGF-family growth factors, and increased expansion of the surface epithelial cell population, which eventually progresses to an invasive gastric carcinoma (Wang et al. 1999). This sequence of events is accelerated by infection with Helicobacter. The loss of parietal cells with prolonged hypergastrinaemia resembles the human condition of atrophic gastritis. It is widely appreciated that reduced acid secretion due to the loss of parietal cells leads in turn to increased plasma gastrin secondary to depression of the acid-inhibitory control mechanisms working on G-cells. In INS-GAS mice, however, moderate hypergastrinaemia precedes the development of atrophic gastritis. At first sight, it would seem to be paradoxical to suggest a causal relationship between elevated plasma gastrin and atrophic gastritis, given the actions of gastrin in increasing parietal cell numbers. It is, however, compatible with the idea that while gastrin initially stimulates parietal cells, with prolonged stimulation there is an upregulation of members of the EGF family of growth factors. The latter provide a local mechanism restraining acid secretion and decreasing parietal cell numbers, while stimulating the growth of surface epithelial cells (Fig. 3C).
Overview and implications
The products of the G-cell act as transepithelial transducers, responsible both for the acute control of gastric secretion and for maintaining the organization of the acid-secreting epithelium. Thus the proliferation and relative proportions of different epithelial cell types are determined by gastrin either directly, or indirectly via locally produced auto- and paracrine growth regulators. There is now a growing recognition that these mechanisms are a component in the pathology of the upper gastrointestinal tract, particularly in conditions involving Helicobacter pylori. Most patients with H. pylori are asymptomatic, but some develop duodenal ulcers and others gastric cancer. Infection with H. pylori is associated with modestly elevated plasma gastrin concentrations (Levi et al. 1989). In part this is likely to be secondary to decreased somatostatin synthesis, since there is reduced somatostatin mRNA abundance in H. pylori infection, which is thought to be attributable to the release of inflammatory mediators such as tumour necrosis factor (TNF)- that inhibit antral D-cell function (Calam et al. 1997). The elevated plasma gastrin stimulates acid secretion, which is a feature of the infection in patients with duodenal ulcers. In other patients, however, moderately elevated plasma gastrin is accompanied by decreased acid secretion, which leads to infection of the corpus and the development of atrophic gastritis, which predisposes to gastric cancer (El-Omar et al. 1997). The results now emerging from physiological studies of the control of gastric epithelial cell function should facilitate an understanding of the mechanisms responsible for major upper gastrointestinal tract diseases.
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Corresponding author
G. J. Dockray: Physiological Laboratory, University of Liverpool, Crown Street, Liverpool L69 3BX, UK.
Email: g.j.dockray{at}liverpool.ac.uk
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