Guanylin and uroguanylin are produced by mouse intestinal epithelial cells of columnar and secretory lineage

Guanylin (GN) and uroguanylin (UGN), through activation of guanylyl cyclase C (GCC), serve to control intestinal fluid homeostasis. Both peptides are produced in the intestinal epithelium, but their cellular origin has not been fully charted. Using quantitative PCR and an improved in situ hybridization technique (RNAscope), we have assessed the expression of GN (Guca2a), UGN (Guca2b), and GCC (Gucy2c) in mouse intestine. In the crypts of Lieberkühn, expression of Guca2a and Guca2b was restricted to cells of secretory lineage, at the crypt’s base, and to a region above, previously identified as a common origin of cellular differentiation. In this compartment, comparatively uniform levels of Guca2a and Guca2b expression were observed throughout the length of the gut. In contrast, Guca2a and Guca2b expression in the villus–surface region was more variable, and reflected the distinct, but overlapping expression pattern observed previously. Accordingly, in jejunum and ileum, Guca2a and Guca2b were abundantly expressed by enterocytes, whereas in colon only Guca2a transcript was found in the surface region. In duodenum, only low levels of Guca2b transcript were observed in columnar cells, and Guca2a expression was restricted entirely to cells of the secretory lineage. Gucy2c was shown to be expressed relatively uniformly along the rostrocaudal and crypt–villus axes and was also found in the duodenal glands. Our study reveals novel aspects of the cellular localization of the GCC signaling axis that, apart from its role in the regulation of fluid balance, link it to pH regulation, cell cycle control, and host defense.

[1]  T. Phillips Both crypt and villus intestinal goblet cells secrete mucin in response to cholinergic stimulation. , 1992, The American journal of physiology.

[2]  D. Goeddel,et al.  Precursor structure, expression, and tissue distribution of human guanylin. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  S. Eber,et al.  Distribution of heat-stable enterotoxin/guanylin receptors in the intestinal tract of man and other mammals. , 1994, Journal of anatomy.

[4]  D. Grube,et al.  Enterochromaffin cells of the digestive system: cellular source of guanylin, a guanylate cyclase-activating peptide. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. Currie,et al.  Immunohistochemical localization of guanylin in the rat small intestine and colon. , 1995, Biochemical and biophysical research communications.

[6]  M. F. Goy,et al.  Guanylin, an endogenous ligand for C-type guanylate cyclase, is produced by goblet cells in the rat intestine. , 1995, Gastroenterology.

[7]  M. Gregor,et al.  Guanylin strongly stimulates rat duodenal HCO3- secretion: proposed mechanism and comparison with other secretagogues. , 1996, Gastroenterology.

[8]  M. Nakazato,et al.  Tissue distribution and plasma concentration of human guanylin. , 1996, Internal medicine.

[9]  M. F. Goy,et al.  Uroguanylin is expressed by enterochromaffin cells in the rat gastrointestinal tract. , 1997, Gastroenterology.

[10]  M. Cohen,et al.  Uroguanylin and guanylin: distinct but overlapping patterns of messenger RNA expression in mouse intestine. , 1997, Gastroenterology.

[11]  N. Joo,et al.  Regulation of intestinal Cl- and[Formula: see text] secretion by uroguanylin. , 1998, American journal of physiology. Gastrointestinal and liver physiology.

[12]  B. Atshaves,et al.  Cellular differentiation and I-FABP protein expression modulate fatty acid uptake and diffusion. , 1998, The American journal of physiology.

[13]  N. Joo,et al.  Regulation of intestinal Cl- and[Formula: see text] secretion by uroguanylin. , 1998, American journal of physiology. Gastrointestinal and liver physiology.

[14]  M. Kuhn,et al.  Regulated, side-directed secretion of proguanylin from isolated rat colonic mucosa. , 1999, Endocrinology.

[15]  M. F. Goy,et al.  Expression of GC-C, a receptor-guanylate cyclase, and its endogenous ligands uroguanylin and guanylin along the rostrocaudal axis of the intestine. , 2000, Endocrinology.

[16]  M. Cohen,et al.  Increases in guanylin and uroguanylin in a mouse model of osmotic diarrhea are guanylate cyclase C-independent. , 2001, Gastroenterology.

[17]  J. Klempnauer,et al.  Guanylin in the human pancreas: a novel luminocrine regulatory pathway of electrolyte secretion via cGMP and CFTR in the ductal system , 2001, Histochemistry and Cell Biology.

[18]  Y. Cetin,et al.  The Electrolyte/Fluid Secretion Stimulatory Peptides Guanylin and Uroguanylin and Their Common Functional Coupling Proteins in the Rat Pancreas: A Correlative Study of Expression and Cell-Specific Localization , 2002, Pancreas.

[19]  D. Witte,et al.  Targeted inactivation of the mouse guanylin gene results in altered dynamics of colonic epithelial proliferation. , 2002, The American journal of pathology.

[20]  L. Gawenis,et al.  cAMP inhibition of murine intestinal Na/H exchange requires CFTR-mediated cell shrinkage of villus epithelium. , 2003, Gastroenterology.

[21]  J. Lorenz,et al.  Uroguanylin knockout mice have increased blood pressure and impaired natriuretic response to enteral NaCl load. , 2003, The Journal of clinical investigation.

[22]  W. Colledge,et al.  Calcium-activated chloride conductance is not increased in pancreatic duct cells of CF mice , 1995, Pflügers Archiv.

[23]  A. Vaandrager Structure and function of the heat-stable enterotoxin receptor/guanylyl cyclase C , 2004, Molecular and Cellular Biochemistry.

[24]  K. Barrett,et al.  A role for guanylate cyclase C in acid-stimulated duodenal mucosal bicarbonate secretion. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[25]  Kozo Nakamura,et al.  Cyclic GMP-dependent protein kinase II is a molecular switch from proliferation to hypertrophic differentiation of chondrocytes. , 2004, Genes & development.

[26]  W. Krause,et al.  Autoradiographic demonstration of specific binding sites for E. coli enterotoxin in various epithelia of the North American opossum , 1990, Cell and Tissue Research.

[27]  L. Hooper,et al.  Symbiotic Bacteria Direct Expression of an Intestinal Bactericidal Lectin , 2006, Science.

[28]  L. Olds,et al.  Spatio-temporal patterns of intestine-specific transcription factor expression during postnatal mouse gut development. , 2006, Gene expression patterns : GEP.

[29]  S. Waldman,et al.  Homeostatic control of the crypt-villus axis by the bacterial enterotoxin receptor guanylyl cyclase C restricts the proliferating compartment in intestine. , 2007, The American journal of pathology.

[30]  Hans Clevers,et al.  SOX9 is required for the differentiation of paneth cells in the intestinal epithelium. , 2006, Gastroenterology.

[31]  G. Flemström,et al.  Duodenal bicarbonate secretion in rats: stimulation by intra‐arterial and luminal guanylin and uroguanylin , 2007, Acta physiologica.

[32]  J. Palazzo,et al.  Guanylyl cyclase C suppresses intestinal tumorigenesis by restricting proliferation and maintaining genomic integrity. , 2007, Gastroenterology.

[33]  M. Manns,et al.  CFTR and its key role in in vivo resting and luminal acid‐induced duodenal HCO3− secretion , 2008, Acta physiologica.

[34]  P. Quinton,et al.  Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion. , 2009, The Journal of clinical investigation.

[35]  W. Weiss,et al.  Cyclic GMP-dependent protein kinase II inhibits cell proliferation, Sox9 expression and Akt phosphorylation in human glioma cell lines , 2009, Oncogene.

[36]  R. Margolskee,et al.  Release of endogenous opioids from duodenal enteroendocrine cells requires Trpm5. , 2009, Gastroenterology.

[37]  Yanfang Guan,et al.  Loss of Guanylyl Cyclase C (GCC) Signaling Leads to Dysfunctional Intestinal Barrier , 2011, PloS one.

[38]  Minmin Luo,et al.  Role for the Membrane Receptor Guanylyl Cyclase-C in Attention Deficiency and Hyperactive Behavior , 2011, Science.

[39]  Hans Clevers,et al.  Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts , 2011, Nature.

[40]  S. Waldman,et al.  A uroguanylin-GUCY2C endocrine axis regulates feeding in mice. , 2011, The Journal of clinical investigation.

[41]  M. Johansson,et al.  Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype , 2012, The Journal of experimental medicine.

[42]  J. Flanagan,et al.  RNAscope: a novel in situ RNA analysis platform for formalin-fixed, paraffin-embedded tissues. , 2012, The Journal of molecular diagnostics : JMD.

[43]  S. Quake,et al.  Identification of a cKit(+) colonic crypt base secretory cell that supports Lgr5(+) stem cells in mice. , 2012, Gastroenterology.

[44]  Rivka Ofir,et al.  Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C. , 2012, American journal of human genetics.

[45]  S. Levy,et al.  Familial diarrhea syndrome caused by an activating GUCY2C mutation. , 2012, The New England journal of medicine.

[46]  T. Freeman,et al.  Identification of Novel Genes Selectively Expressed in the Follicle-Associated Epithelium from the Meta-Analysis of Transcriptomics Data from Multiple Mouse Cell and Tissue Populations , 2012, DNA research : an international journal for rapid publication of reports on genes and genomes.

[47]  F. Hofmann,et al.  Type 2 cGMP-dependent protein kinase regulates proliferation and differentiation in the colonic mucosa. , 2012, American journal of physiology. Gastrointestinal and liver physiology.

[48]  E. Mann,et al.  Guanylate cyclase C limits systemic dissemination of a murine enteric pathogen , 2013, BMC Gastroenterology.

[49]  Thomas D. Schmittgen,et al.  RNA isolation from mouse pancreas: a ribonuclease-rich tissue. , 2014, Journal of visualized experiments : JoVE.

[50]  J. Kaunitz,et al.  Duodenal luminal nutrient sensing. , 2014, Current opinion in pharmacology.

[51]  A. Franke,et al.  Congenital secretory diarrhoea caused by activating germline mutations in GUCY2C , 2015, Gut.

[52]  Olga Kovbasnjuk,et al.  Human Enteroids as a Model of Upper Small Intestinal Ion Transport Physiology and Pathophysiology. , 2016, Gastroenterology.