Use of organoids to study regenerative responses to intestinal damage

被引:19
作者
Blutt, Sarah E. [1 ]
Klein, Ophir D. [2 ,3 ,4 ,5 ]
Donowitz, Mark [6 ,7 ]
Shroyer, Noah [8 ,9 ,10 ]
Guha, Chandan [11 ]
Estes, Mary K. [1 ,8 ,9 ,10 ]
机构
[1] Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[2] Univ Calif San Francisco, Dept Orofacial Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Program Craniofacial Biol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
[6] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Med, Gastroenterol & Hepatol Div, Baltimore, MD 21205 USA
[8] Baylor Coll Med, Dept Med, Div Gastroenterol, Houston, TX 77030 USA
[9] Baylor Coll Med, Dept Med, Div Hepatol, Houston, TX 77030 USA
[10] Baylor Coll Med, Dept Med, Div Infect Dis, Houston, TX 77030 USA
[11] Albert Einstein, Dept Radiat Oncol, Bronx, NY USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2019年 / 317卷 / 06期
关键词
enteroids; intestinal stem cell; organoids; regeneration; ENTERICA SEROVAR TYPHIMURIUM; LABEL-RETAINING CELLS; STEM-CELLS; IN-VITRO; FUNCTIONALLY DISTINCT; SECRETORY PRECURSORS; CRYPT REGENERATION; MICROBIOTA; EXPANSION; COLON;
D O I
10.1152/ajpgi.00346.2018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Intestinal organoid cultures provide an in vitro model system for studying pathways and mechanisms involved in epithelial damage and repair. Derived from either embryonic or induced pluripotent stem cells or adult intestinal stem cells or tissues, these self-organizing, multicellular structures contain polarized mature cells that recapitulate both the physiology and heterogeneity of the intestinal epithelium. These cultures provide a cutting-edge technology for defining regenerative pathways that are induced following radiation or chemical damage, which directly target the cycling intestinal stem cell, or damage resulting from viral, bacterial, or parasitic infection of the epithelium. Novel signaling pathways or biological mechanisms identified from organoid studies that mediate regeneration of the epithelium following damage are likely to be important targets of preventive or therapeutic modalities to mitigate intestinal injury. The evolution of these cultures to include more components of the intestinal wall and the ability to genetically modify them are key components for defining the mechanisms that modulate epithelial regeneration.
引用
收藏
页码:G845 / G852
页数:8
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