| Literature DB >> 30917322 |
Olga N Karpus1, B Florien Westendorp2, Jacqueline L M Vermeulen2, Sander Meisner2, Jan Koster3, Vanesa Muncan2, Manon E Wildenberg2, Gijs R van den Brink4.
Abstract
Intestinal epithelial cells have a defined hierarchy with stem cells located at the bottom of the crypt and differentiated cells more at the top. Epithelial cell renewal and differentiation are strictly controlled by various regulatory signals provided by epithelial as well as surrounding cells. Although there is evidence that stromal cells contribute to the intestinal stem cell niche, their markers and the soluble signals they produce have been incompletely defined. Using a number of established stromal cell markers, we phenotypically and functionally examined fibroblast populations in the colon. CD90+ fibroblasts located in close proximity to stem cells in vivo support organoid growth in vitro and express crucial stem cell growth factors, such as Grem1, Wnt2b, and R-spondin3. Moreover, we found that CD90+ fibroblasts express a family of proteins-class 3 semaphorins (Sema3)-that are required for the supportive effect of CD90+ fibroblasts on organoid growth.Entities:
Keywords: CD90; Gli1; Nrp2; colon; fibroblast; intestine; niche; semaphorin; stem cell; stroma
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Year: 2019 PMID： 30917322 DOI： 10.1016/j.celrep.2019.02.101
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423