Clonal origin of columnar, mucous, and endocrine cell lineages in human colorectal epithelium
- PMID: 2449944
- DOI: 10.1002/1097-0142(19880401)61:7<1359::aid-cncr2820610714>3.0.co;2-0
Clonal origin of columnar, mucous, and endocrine cell lineages in human colorectal epithelium
Abstract
Human colorectal epithelium is composed mainly of columnar, mucous and endocrine cells; origin of these cell lineages from a multi-potential stem cell at the base of the crypt (the Unitarian hypothesis) has been proposed but not yet demonstrated. Gut endocrine cells have variously been considered of neural crest or endodermal origin, but conclusive evidence, particularly in humans, is lacking. It has been shown that in mouse gastrointestinal tract, a single progenitor cell gives rise to both columnar and mucous cells, but it has yet to be demonstrated that such a progenitor cell can also give rise to endocrine cells. Here, a single human rectal adenocarcinoma cell has been shown to differentiate into columnar, mucous and endocrine cells; therefore all epithelial lineages are of clonal origin. Additionally, these results show that human colorectal enteroendocrine cells, at least in neoplastic epithelium, have an endodermal origin.
Similar articles
-
Endocrine and mucous differentiation by a cloned human rectal adenocarcinoma cell line (HRA-19) in vitro: inhibition by TGF-beta 1.J Cell Sci. 1994 Apr;107 ( Pt 4):1041-6. doi: 10.1242/jcs.107.4.1041. J Cell Sci. 1994. PMID: 8056828
-
The endodermal origin of the endocrine cells of an adenocarcinoma of the colon of the rat.Cancer. 1982 Oct 15;50(8):1530-8. doi: 10.1002/1097-0142(19821015)50:8<1530::aid-cncr2820500813>3.0.co;2-9. Cancer. 1982. PMID: 7116287
-
The stem-cell zone of the small intestinal epithelium. III. Evidence from columnar, enteroendocrine, and mucous cells in the adult mouse.Am J Anat. 1981 Jan;160(1):77-91. doi: 10.1002/aja.1001600107. Am J Anat. 1981. PMID: 7211718
-
Investigating the fixation and spread of mutations in the gastrointestinal epithelium.Future Oncol. 2008 Dec;4(6):825-39. doi: 10.2217/14796694.4.6.825. Future Oncol. 2008. PMID: 19086849 Review.
-
Differentiation pathways and histogenetic aspects of normal and abnormal prostatic growth: a stem cell model.Prostate. 1996 Feb;28(2):98-106. doi: 10.1002/(SICI)1097-0045(199602)28:2<98::AID-PROS4>3.0.CO;2-J. Prostate. 1996. PMID: 8604398 Review.
Cited by
-
c-myc antisense oligonucleotides inhibit the colony-forming capacity of Colo 320 colonic carcinoma cells.J Clin Invest. 1992 May;89(5):1523-7. doi: 10.1172/JCI115744. J Clin Invest. 1992. PMID: 1569190 Free PMC article.
-
Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implications for neuroendocrine cell survival.J Clin Invest. 1997 Jun 15;99(12):2979-91. doi: 10.1172/JCI119493. J Clin Invest. 1997. PMID: 9185522 Free PMC article.
-
The prevalence and clinical significance of chromogranin A and secretogranin II immunoreactivity in colorectal adenocarcinomas.Virchows Arch. 1995;426(6):587-92. doi: 10.1007/BF00192113. Virchows Arch. 1995. PMID: 7655739
-
Neuroendocrine cells in the normal, hyperplastic and neoplastic prostate.Urol Res. 1995;22(6):333-41. doi: 10.1007/BF00296871. Urol Res. 1995. PMID: 7740652 Review.
-
Development of colonic and pancreatic endocrine tumours in mice expressing a glucagon-SV40 T antigen transgene.Virchows Arch. 1996 Mar;427(6):595-606. doi: 10.1007/BF00202891. Virchows Arch. 1996. PMID: 8605571
Publication types
MeSH terms
LinkOut - more resources
Research Materials