Identification of a putative intestinal stem cell and early lineage marker; Musashi-1

被引:398
作者
Potten, CS
Booth, C
Tudor, GL
Booth, D
Brady, G
Hurley, P
Ashton, G
Clarke, R
Sakakibara, S
Okano, H
机构
[1] EpiStem Ltd, Manchester M13 9XX, Lancs, England
[2] Christie Hosp NHS Trust, Paterson Inst Canc Res, Epithelial Biol Dept, Manchester M20 4BX, Lancs, England
[3] Christie Hosp NHS Trust, Paterson Inst Canc Res, Dept Histol, Manchester M20 4BX, Lancs, England
[4] Christie Hosp NHS Trust, Paterson Inst Canc Res, Dept Clin Res, Manchester M20 4BX, Lancs, England
[5] Osaka Univ, Dept Neuroanat, Biomed Res Ctr, Suita, Osaka 565, Japan
[6] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Minoto Ku, Tokyo 1050011, Japan
[7] Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, Tokyo 1608582, Japan
[8] Paterson Inst Canc Res, Canc Res Campaign, Manchester, Lancs, England
关键词
stem cells; small intestine; clonogenic cells; Musashi-1; stem cell marker;
D O I
10.1046/j.1432-0436.2003.700603.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There are few reliable markers for adult stem cells and none for those of the intestinal epithelium. Previously, indirect experimental approaches have predicted stem cell position and numbers. The Musashi-1 (Msi-1) gene encodes an RNA binding protein associated with asymmetric divisions in neural progenitor cells. Two-day-old, adult, and 4.5 h, 1-, 2-, 4- and 12-day postirradiation samples of 1313171 mouse small intestine, together with some samples of mouse colon were stained with a rat monoclonal antibody to Musashi-1 (14 H-1). Min ( + / -) mice with small intestinal adenomas of varying sizes were also analysed. Samples of human small and large bowel were also studied but the antibody staining was weak. Musashi-1 expression was observed using immunohistochemistry in neonatal, adult, and regenerating crypts with a staining pattern consistent with the predicted number and distribution of early lineage cells including the functional stein cells in these situations. Early dysplastic crypts and adenomas were also strongly Musashi-1 positive. In situ hybridization studies showed similar expression patterns for the Musashi mRNA and real-time quantitative RT-PCR showed dramatically more Msi-1 mRNA expression in Min tumours compared with adjacent normal tissue. These observations suggest that Musashi-1 is a marker of stem and early lineage progenitor cells in murine intestinal tissue.
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页码:28 / 41
页数:14
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