| Literature DB >> 28210941 |
Fengge Zhu1, Xueyuan Bai2, Xiangmei Chen3.
Abstract
Fibrosis is defined as an excessive deposition of extracellular matrix (ECM), which leads to the destruction of organ structure and impairment of organ function. Fibrosis occurs not only in kidney but also in lung, liver, heart, and skin. Common pathways of fibrosis are thought to exist. Renal interstitial fibrosis is a complex process that involves multiple molecular signaling and multiple cellular components, in which B cells appear to be one of the emerging important players. B cells may affect fibrosis through cytokine production and through interaction with other cells including fibroblasts, macrophages and T cells. This review summarizes recent research findings of B cells in fibrosis and provides an insight of how the future therapeutics of fibrosis could be developed from a B-cell point of view.Entities:
Keywords: B cell; B lymphocyte; Inflammation; Renal interstitial fibrosis
Year: 2017 PMID: 28210941 PMCID: PMC5559395 DOI: 10.1007/s12079-017-0382-x
Source DB: PubMed Journal: J Cell Commun Signal ISSN: 1873-9601 Impact factor: 5.782