Distinct SOX9 levels differentially mark stem/progenitor populations and enteroendocrine cells of the small intestine epithelium

被引:180
作者
Formeister, Eric J. [1 ]
Sionas, Ayn L. [1 ]
Lorance, David K. [1 ]
Barkley, Carey L. [1 ]
Lee, Ginny H. [1 ]
Magness, Scott T. [1 ]
机构
[1] Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27599 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2009年 / 296卷 / 05期
基金
美国国家卫生研究院;
关键词
intestinal epithelial development; stem cell; progenitor cell; MOUSE SMALL INTESTINE; STEM-CELL; TRANSCRIPTION FACTORS; CAMPOMELIC DYSPLASIA; ENDOCRINE-CELLS; BETA-CATENIN; PANETH CELLS; MUCOUS CELLS; RENEWAL; ORIGIN;
D O I
10.1152/ajpgi.00004.2009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Formeister EJ, Sionas AL, Lorance DK, Barkley CL, Lee GH, Magness ST. Distinct SOX9 levels differentially mark stem/progenitor populations and enteroendocrine cells of the small intestine epithelium. Am J Physiol Gastrointest Liver Physiol 296: G1108-G1118, 2009. First published February 19, 2009; doi:10.1152/ajpgi.00004.2009.-SOX transcription factors have the capacity to modulate stem/progenitor cell proliferation and differentiation in a dose-dependent manner. SOX9 is expressed in the small intestine epithelial stem cell zone. Therefore, we hypothesized that differential levels of SOX9 may exist, influencing proliferation and/or differentiation of the small intestine epithelium. Sox9 expression levels in the small intestine were investigated using a Sox9 enhanced green fluorescent protein (Sox9(EGFP)) transgenic mouse. Sox9(EGFP) levels correlate with endogenous SOX9 levels, which are expressed at two steady-state levels, termed Sox9(EGFPLO) and Sox9(EGFPHI). Crypt-based columnar cells are Sox9(EGFPLO) and demonstrate enriched expression of the stem cell marker, Lgr5. Sox9(EGFPHI) cells express chromogranin A and substance P but do not express Ki67 and neurogenin3, indicating that Sox9(EGFPHI) cells are postmitotic enteroendocrine cells. Overexpression of SOX9 in a crypt cell line stopped proliferation and induced morphological changes. These data support a bimodal role for SOX9 in the intestinal epithelium, where low SOX9 expression supports proliferative capacity, and high SOX9 expression suppresses proliferation.
引用
收藏
页码:G1108 / G1118
页数:11
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