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LRCH1 suppresses migration of CD4(+) T cells and refers to disease activity in ulcerative colitis

Background: Ulcerative colitis (UC) is a chronically remittent and progressive inflammatory disorder. LRCH1 is reported to be involved in the immune-regulation of several diseases. However, the exact roles of LRCH1 in UC are still obscure. Materials and Methods: LRCH1 expression was analyzed in the...

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Detalles Bibliográficos
Autores principales: Wang, Yibo, Zhang, Hairong, He, Heng, Ai, Kuankuan, Yu, Wei, Xiao, Xiao, Qin, Yufen, Zhang, Lingming, Xiong, Huabao, Zhou, Guangxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085219/
https://www.ncbi.nlm.nih.gov/pubmed/32210709
http://dx.doi.org/10.7150/ijms.39106
Descripción
Sumario:Background: Ulcerative colitis (UC) is a chronically remittent and progressive inflammatory disorder. LRCH1 is reported to be involved in the immune-regulation of several diseases. However, the exact roles of LRCH1 in UC are still obscure. Materials and Methods: LRCH1 expression was analyzed in the inflamed mucosa and peripheral blood mononuclear cells (PBMCs) from patients with UC by quantitative RT-PCR and immunohistochemistry. Peripheral blood CD4(+) T cells were transfected with lentivirus-expressing LRCH1 (LV-LRCH1) or LV-sh-LRCH1, and cytokine expression was determined by using flow cytometry, quantitative RT-PCR and ELISA. Transfected CD4(+) T cells were harvested to examine the capacity of chemotaxis using Transwell plate. Results: LRCH1 expression was highly decreased in colonic mucosa and PBMCs from patients with A-UC, and negatively correlated with disease activity. Up or down regulation of LRCH1 did not affect the differentiation of CD4(+) T cells, and the related cytokines expression. Moreover, LRCH1 inhibited migratory capacity of CD4(+) T cells toward CXCL12 by PKCα. Conclusion: LRCH1 plays an important role in the pathogenesis of UC, possibly through modulating the migration of CD4(+) T cells. Therefore, targeting LRCH1 might serve as a novel therapeutic approach in the management of UC.