Epithelial stem cell repertoire in the gut: clues to the origin of cell lineages, proliferative units and cancer

Gastrointestinal stem cells are shown to be pluripotential and to give rise to all cell lineages in the epithelium. After damage, gut stem cells produce reparative cell lineages that produce a wide range of peptides with important actions on cell proliferation and migration, and promote regeneration and healing. Increase in stem cell number is considered to induce crypt fission, and lead to increases in the number of crypts, even in the adult; it is also the mode of spread of mutated clones in the colorectal mucosa. Stem cell repertoire is defined by both intrinsic programming of the stem cell itself, but signalling from the mesenchyme is also vitally important for defining both stem cell progeny and proliferation. Carcinogenesis in the colon occurs through sequential mutations, possibly occurring in a single cell. A case is made for this being the stem cell, but recent studies indicate that several stem cells may need to be so involved, since early lesions appear to be polyclonal in derivation.

[1]  P. Masson Carcinoids (Argentaffin-Cell Tumors) and Nerve Hyperplasia of the Appendicular Mucosa. , 1928, The American journal of pathology.

[2]  H. Tesluk,et al.  Brunner-type glands in regional enteritis. , 1955, Gastroenterology.

[3]  F. Lee PYLORIC METAPLASIA IN THE SMALL INTESTINE. , 1964, The Journal of pathology and bacteriology.

[4]  M. Lyon Lack of evidence that inactivation of the mouse X-chromosome is incomplete. , 1966, Genetical research.

[5]  A. Pearse Common cytochemical properties of cells producing polypeptide hormones, with particular reference to calcitonin and the thyroid C cells , 1966, Veterinary Record.

[6]  A. Pearse 5-Hydroxytryptophan Uptake by Dog Thyroid ‘C’ Cells, and its Possible Significance in Polypeptide Hormone Production , 1966, Nature.

[7]  E. Beutler,et al.  Value of genetic variants of glucose-6-phosphate dehydrogenase in tracing the origin of malignant tumors. , 1967, The New England journal of medicine.

[8]  S. Gartler,et al.  Clonal origin of chronic myelocytic leukemia in man. , 1967, Proceedings of the National Academy of Sciences of the United States of America.

[9]  A. Pearse,et al.  THE CYTOCHEMISTRY AND ULTRASTRUCTURE OF POLYPEPTIDE HORMONE-PRODUCING CELLS OF THE APUD SERIES AND THE EMBRYOLOGIC, PHYSIOLOGIC AND PATHOLOGIC IMPLICATIONS OF THE CONCEPT , 1969, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[10]  C. Lelièvre,et al.  Démonstration de l'origine neurale des cellules à calcitonine du corps ultimobranchial chez l'embryon de poulet. , 1970 .

[11]  H. Withers,et al.  Microcolony survival assay for cells of mouse intestinal mucosa exposed to radiation. , 1970, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[12]  H. Suzuki,et al.  Differentiation of Immature Mucous Cells into Parietal, Argyrophil, and Chief Cells in Stomach Grafts , 1970, Science.

[13]  E. Fisher,et al.  Histogenetic Relationship Between Carcinoids and Mucin-secreting Carcinomas of Colon as Revealed by Heterotransplantation , 1970, British Journal of Cancer.

[14]  N. L. Le Douarin,et al.  The migration of neural crest cells to the wall of the digestive tract in avian embryo. , 1973, Journal of embryology and experimental morphology.

[15]  A. Andrew Further evidence that enterochromaffin cells are not derived from the neural crest. , 1974, Journal of embryology and experimental morphology.

[16]  C. P. Leblond,et al.  Origin, differentiation and renewal of the four main epithelial cell types in the mouse small intestine. V. Unitarian Theory of the origin of the four epithelial cell types. , 1974, The American journal of anatomy.

[17]  A. Knudson Heredity and human cancer. , 1974, The American journal of pathology.

[18]  A. Cairnie,et al.  FISSION OF CRYPTS IN THE SMALL INTESTINE OF THE IRRADIATED MOUSE , 1975, Cell and tissue kinetics.

[19]  P. Fialkow Clonal origin of human tumors. , 1976, Biochimica et biophysica acta.

[20]  J. Hirsch,et al.  Adipose tissue cellularity in human obesity. , 1976, Clinics in endocrinology and metabolism.

[21]  G. Mcdonald,et al.  Mucinous carcinoid tumour of the appendix containing paneth cells , 1977, Irish journal of medical science.

[22]  C. Potten,et al.  Stem cells and tissue homeostasis , 1978 .

[23]  O. Kobori,et al.  Neuroendocrine cells in serially passaged rat stomach cancers induced by MNNG , 1979, International journal of cancer.

[24]  L. Lajtha,et al.  A comparison of cell replacement in bone marrow, testis and three regions of surface epithelium. , 1979, Biochimica et biophysica acta.

[25]  A. Maskens,et al.  KINETICS OF TISSUE PROLIFERATION IN COLORECTAL MUCOSA DURING POST‐NATAL GROWTH , 1981, Cell and tissue kinetics.

[26]  P. Isaacson Crypt cell carcinoma of the appendix (so‐called adenocarcinoid tumor) , 1981, The American journal of surgical pathology.

[27]  L. Kostović-Knežević,et al.  Morphogenetic behaviour of the rat embryonic ectoderm as a renal homograft. , 1981, Journal of embryology and experimental morphology.

[28]  W. F. Cox,et al.  The endodermal origin of the endocrine cells of an adenocarcinoma of the colon of the rat , 1982, Cancer.

[29]  N. Wright,et al.  The kinetics of villus cell populations in the mouse small intestine , 1982, Cell and tissue kinetics.

[30]  S. Hamilton,et al.  Multiclonal origin of polyps in Gardner syndrome. , 1983, Science.

[31]  N. Wright,et al.  Intravenous but not intragastric urogastrone-EGF is trophic to the intestine of parenterally fed rats , 1984, Regulatory Peptides.

[32]  Books ReviewedBook Review1983 YEAR BOOK of Urology, Jay Y. Gillenwater, Stuart S. Howards (Eds.), Year Book Medical Publishers, Inc, Chicago and London (1984), $39.95 , 1984 .

[33]  P. Alexander Do cancers arise from a single transformed cell or is monoclonality of tumours a late event in carcinogenesis? , 1985, British Journal of Cancer.

[34]  H. Rubin Cancer as a dynamic developmental disorder. , 1985, Cancer research.

[35]  M. Dunnill,et al.  Human lung tumours: a correlation of antigenic profile with histological type , 1985, Histopathology.

[36]  B. Ponder,et al.  Derivation of mouse intestinal crypts from single progenitor cells , 1985, Nature.

[37]  B. Ponder,et al.  Direct examination of the clonality of carcinogen-induced colonic epithelial dysplasia in chimeric mice. , 1986, Journal of the National Cancer Institute.

[38]  H. Hauri,et al.  Fetal gut mesenchyme induces differentiation of cultured intestinal endodermal and crypt cells. , 1986, Developmental biology.

[39]  M. Kedinger,et al.  Importance of a fibroblastic support for in vitro differentiation of intestinal endodermal cells and for their response to glucocorticoids. , 1987, Cell differentiation.

[40]  B. Vogelstein,et al.  Clonal analysis of human colorectal tumors. , 1987, Science.

[41]  H Cheng,et al.  The crypt cycle. Crypt and villus production in the adult intestinal epithelium. , 1987, Biophysical journal.

[42]  B. Ponder,et al.  Development of the pattern of cell renewal in the crypt-villus unit of chimaeric mouse small intestine. , 1988, Development.

[43]  S. Kirkland Clonal origin of columnar, mucous, and endocrine cell lineages in human colorectal epithelium , 1988, Cancer.

[44]  R. Scothorne The borderland of embryology and pathology in the gut epithelium , 1988, Histopathology.

[45]  G. Williams,et al.  Demonstration of somatic mutation and colonic crypt clonality by X-linked enzyme histochemistry , 1988, Nature.

[46]  F. Bosman Endocrine cells in non‐endocrine tumours , 1989, The Journal of pathology.

[47]  C. Fuller,et al.  Crypt restricted heterogeneity of goblet cell mucus glycoprotein in histologically normal human colonic mucosa: a potential marker of somatic mutation. , 1990, British Journal of Cancer.

[48]  N. Wright,et al.  Ulceration induces a novel epidermal growth factor-secreting cell lineage in human gastrointestinal mucosa. , 1990, Digestion.

[49]  M. Surani,et al.  Gastric endocrine cells share a clonal origin with other gut cell lineages. , 1990, Development.

[50]  P. Chambon,et al.  Epidermal growth factor (EGF/URO) induces expression of regulatory peptides in damaged human gastrointestinal tissues , 1990, The Journal of pathology.

[51]  D. Winton,et al.  Stem-cell organization in mouse small intestine , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[52]  G. Schmidt,et al.  On the clonal origin of tumours--lessons from studies of intestinal epithelium. , 1990, BioEssays : news and reviews in molecular, cellular and developmental biology.

[53]  M. Loeffler,et al.  Stem cells: attributes, cycles, spirals, pitfalls and uncertainties. Lessons for and from the crypt. , 1990, Development.

[54]  N. Wright,et al.  Induction of a novel epidermal growth factor-secreting cell lineage by mucosal ulceration in human gastrointestinal stem cells , 1990, Nature.

[55]  N. Wright,et al.  Effects of urogastrone-epidermal growth factor on intestinal brush border enzymes and mitotic activity. , 1991, Gut.

[56]  Patricia L. Blount,et al.  Distribution of aneuploid cell populations in ulcerative colitis with dysplasia or cancer. , 1991, Gastroenterology.

[57]  G. Stamp,et al.  Lysozyme gene expression in inflammatory bowel disease. , 1992, Gastroenterology.

[58]  J. Gordon,et al.  Use of fetal intestinal isografts from normal and transgenic mice to study the programming of positional information along the duodenal-to-colonic axis. , 1992, The Journal of biological chemistry.

[59]  J. Gordon,et al.  The Min (multiple intestinal neoplasia) mutation: its effect on gut epithelial cell differentiation and interaction with a modifier system , 1992, The Journal of cell biology.

[60]  G. Williams,et al.  A stem cell niche theory of intestinal crypt maintenance based on a study of somatic mutation in colonic mucosa. , 1992, The American journal of pathology.

[61]  D. Ahnen Abnormal DNA content as a biomarker of large bowel cancer risk and prognosis , 1992, Journal of cellular biochemistry. Supplement.

[62]  J. Hendry,et al.  The clonogen content of murine intestinal crypts: dependence on radiation dose used in its determination. , 1992, Radiation research.

[63]  D. Ahnen,et al.  Proliferating cell nuclear antigen expression in normal, preneoplastic, and neoplastic colonic epithelium of the rat. , 1992, Gastroenterology.

[64]  K. Fleming,et al.  A nude mouse xenograft model of fetal intestine development and differentiation. , 1992, Development.

[65]  D. Rubin Spatial analysis of transcriptional activation in fetal rat jejunal and ileal gut epithelium. , 1992, The American journal of physiology.

[66]  E G Luebeck,et al.  Multistage carcinogenesis: population-based model for colon cancer. , 1992, Journal of the National Cancer Institute.

[67]  P. Rabinovitch,et al.  Neoplastic progression in ulcerative colitis: histology, DNA content, and loss of a p53 allele. , 1992, Gastroenterology.

[68]  C. P. Leblond,et al.  Dynamics of epithelial cells in the corpus of the mouse stomach. I. Identification of proliferative cell types and pinpointing of the stem cell , 1993, The Anatomical record.

[69]  M. Loeffler,et al.  Somatic mutation, monoclonality and stochastic models of stem cell organization in the intestinal crypt. , 1993, Journal of theoretical biology.

[70]  R. Poulsom,et al.  hP1.B, a human P-domain peptide homologous with rat intestinal trefoil factor, is expressed also in the ulcer-associated cell lineage and the uterus. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[71]  G. Stamp,et al.  Trefoil peptide gene expression in gastrointestinal epithelial cells in inflammatory bowel disease. , 1993, Gastroenterology.

[72]  M. Tatematsu,et al.  Clonal analysis of glandular stomach carcinogenesis in C3H/HeN<==>BALB/c chimeric mice treated with N-methyl-N-nitrosourea. , 1994, Cancer letters.

[73]  S. Kirkland,et al.  Endocrine and mucous differentiation by a cloned human rectal adenocarcinoma cell line (HRA-19) in vitro: inhibition by TGF-beta 1. , 1994, Journal of cell science.

[74]  D. Ahnen,et al.  The kinetic organization of the ulcer-associated cell lineage (UACL): delineation of a novel putative stem-cell region. , 1994, Epithelial cell biology.

[75]  J. Gordon,et al.  Use of isografts to study proliferation and differentiation programs of mouse stomach epithelia. , 1994, The American journal of physiology.

[76]  Geraint T. Williams,et al.  Human colonic stem cell mutation frequency with and without irradiation , 1994, The Journal of pathology.

[77]  P. Chambon,et al.  The ulceration‐associated cell lineage (UACL) reiterates the Brunner's gland differentiation programme but acquires the proliferative organization of the gastric gland , 1994, The Journal of pathology.

[78]  J. Jass,et al.  Colorectal mucin histochemistry in health and disease: A critical review , 1994, Pathology international.

[79]  N. Wright,et al.  Crypt fission in the small intestine and colon. A mechanism for the emergence of G6PD locus-mutated crypts after treatment with mutagens. , 1995, The American journal of pathology.

[80]  J. Heddle,et al.  The induction of dominant somatic mutations at the Dlb-1 locus. , 1995, Mutation research.

[81]  M. Bjerknes The crypt cycle and the asymptotic dynamics of the proportion of differently sized mutant crypt clones in the mouse intestine , 1995, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[82]  R. Hargest,et al.  Expression of the APC gene after transfection into a colonic cancer cell line. , 1995, Gut.

[83]  R. Poulsom,et al.  Trefoil peptides , 1999, Bailliere's clinical gastroenterology.

[84]  M. Kaminishi,et al.  Clonal analysis of isolated single fundic and pyloric gland of stomach using X-linked polymorphism. , 1996, Biochemical and biophysical research communications.

[85]  M. Bjerknes Expansion of mutant stem cell populations in the human colon. , 1996, Journal of theoretical biology.

[86]  W. Bodmer,et al.  Polyclonal Origin of Colonic Adenomas in an XO/XY Patient with FAP , 1996, Science.

[87]  R. Nusse,et al.  Wnt signaling: a common theme in animal development. , 1997, Genes & development.

[88]  H. Edlund,et al.  Sonic hedgehog directs specialised mesoderm differentiation in the intestine and pancreas , 1997, Current Biology.

[89]  N. Wright 10 – Stem cell repertoire in the intestine* , 1997 .

[90]  K. Kaestner,et al.  The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestinal proliferation and differentiation. , 1997, Genes & development.

[91]  S. Gallinger,et al.  APC mutation and the crypt cycle in murine and human intestine. , 1997, The American journal of pathology.

[92]  W. Dove,et al.  Localized gene action controlling intestinal neoplasia in mice. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[93]  U. Paulus,et al.  Clonality and life cycles of intestinal crypts explained by a state dependent stochastic model of epithelial stem cell organization. , 1997, Journal of Theoretical Biology.

[94]  T. Noda,et al.  Rapid colorectal adenoma formation initiated by conditional targeting of the Apc gene. , 1997, Science.

[95]  J. Wilson,et al.  Making space for intestinal gene therapy. , 1997, Gastroenterology.

[96]  A. Merritt,et al.  Polyclonal structure of intestinal adenomas in ApcMin/+ mice with concomitant loss of Apc+ from all tumor lineages. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[97]  L. Aaltonen,et al.  Tracing cell fates in human colorectal tumors from somatic microsatellite mutations: evidence of adenomas with stem cell architecture. , 1998, The American journal of pathology.

[98]  N. de Wind,et al.  Mouse models for hereditary nonpolyposis colorectal cancer. , 1998, Cancer research.

[99]  J. Gordon,et al.  Effects of Forced Expression of an NH2-terminal Truncated β-Catenin on Mouse Intestinal Epithelial Homeostasis , 1998, The Journal of cell biology.

[100]  Hans Clevers,et al.  Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4 , 1998, Nature Genetics.

[101]  H Clevers,et al.  Two Members of the Tcf Family Implicated in Wnt/β-Catenin Signaling during Embryogenesis in the Mouse , 1998, Molecular and Cellular Biology.

[102]  B. B. Rawdon,et al.  The origin of gut and pancreatic neuroendocrine (APUD) cells—the last word? , 1998, The Journal of pathology.

[103]  W. Bodmer,et al.  APC in the regulation of intestinal crypt fission , 1998, The Journal of pathology.

[104]  H. Esumi,et al.  Lineage and clonal development of gastric glands. , 1998, Developmental biology.

[105]  A. Sparks,et al.  Identification of c-MYC as a target of the APC pathway. , 1998, Science.

[106]  THE ORIGIN OF GUT AND PANCREATIC NEUROENDOCRINE (APUD) CELLS , 1999 .

[107]  N. Wright Letter from Waldum et al. commenting on the editorial by Andrew et al and responses , 1999, The Journal of pathology.

[108]  R. Playford,et al.  Reprogramming of intestinal differentiation and intercalary regeneration in Cdx2 mutant mice. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[109]  H Cheng,et al.  Clonal analysis of mouse intestinal epithelial progenitors. , 1999, Gastroenterology.

[110]  H. Krokan,et al.  Re. Editorial entitled ‘The origin of gut and pancreatic neuroendocrine (APUD) cells—the last word?’ , 1999, The Journal of pathology.

[111]  N. Wright,et al.  Field cancerization, clonality, and epithelial stem cells: the spread of mutated clones in epithelial sheets , 1999, The Journal of pathology.

[112]  M. Seldin,et al.  Colonic hamartoma development by anomalous duplication in Cdx2 knockout mice. , 1999, Cancer research.