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Intestinal Lymphatic Endothelial Cells Produce R-Spondin3

The R-Spondin (R-Spo) family regulates WNT signaling and stimulates the proliferation and differentiation of intestinal stem cells (ISCs). R-Spo plays a critical role in maintaining intestinal homeostasis, but endogenous producers of R-Spo in the intestine remain to be investigated. We found that R-...

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Detalles Bibliográficos
Autores principales: Ogasawara, Reiki, Hashimoto, Daigo, Kimura, Shunsuke, Hayase, Eiko, Ara, Takahide, Takahashi, Shuichiro, Ohigashi, Hiroyuki, Yoshioka, Kosuke, Tateno, Takahiro, Yokoyama, Emi, Ebata, Ko, Kondo, Takeshi, Sugita, Junichi, Onozawa, Masahiro, Iwanaga, Toshihiko, Teshima, Takanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048029/
https://www.ncbi.nlm.nih.gov/pubmed/30013036
http://dx.doi.org/10.1038/s41598-018-29100-7
Descripción
Sumario:The R-Spondin (R-Spo) family regulates WNT signaling and stimulates the proliferation and differentiation of intestinal stem cells (ISCs). R-Spo plays a critical role in maintaining intestinal homeostasis, but endogenous producers of R-Spo in the intestine remain to be investigated. We found that R-Spo3 was the major R-Spo family member produced in the intestine and it was predominantly produced by CD45(−)CD90(+)CD31(+) lymphatic endothelial cells (LECs) in the lamina propria of the intestinal mucosa. Transcriptome analysis demonstrated that LECs highly expressed R-Spo receptor, Lgr5, suggesting an autocrine stimulatory loop in LECs. LECs were significantly reduced in number, and their R-Spo3 production was impaired in intestinal graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation. The impaired production of R-Spo3 in the intestine may be a novel mechanism of delayed tissue repair and defective mucosal defense in intestinal GVHD. We demonstrate a novel role of intestinal LECs in producing R-Spondin3 to maintain intestinal homeostasis.