Kloc Malgorzata, Kubiak Jacek Z, Li Xian C, Ghobrial Rafik M
1 The Houston Methodist Research Institute, Houston, TX. 2 CNRS/University Rennes1 UMR 6290, Institute of Genetics and Development of Rennes, Cell Cycle Group, Faculty of Medicine, 35-043 Rennes, France.
Transplantation. 2015 Apr;99(4):658-67. doi: 10.1097/TP.0000000000000648.
Chronic rejection of transplanted organs remains the main obstacle in the long-term success of organ transplantation. Thus, there is a persistent quest for development of antichronic rejection therapies and identification of novel molecular and cellular targets. One of the potential targets is the pericytes, the mural cells of microvessels, which regulate microvascular permeability, development, and maturation by controlling endothelial cell functions and regulating tissue fibrosis and inflammatory response. In this review, we discuss the potential of targeting pericytes in the development of microvasular dysfunction and the molecular pathways involved in regulation of pericyte activities for antichronic rejection intervention.
移植器官的慢性排斥反应仍然是器官移植长期成功的主要障碍。因此,人们一直在不断寻求开发抗慢性排斥反应的疗法,并寻找新的分子和细胞靶点。潜在靶点之一是周细胞,即微血管的壁细胞,它通过控制内皮细胞功能以及调节组织纤维化和炎症反应来调节微血管通透性、发育和成熟。在这篇综述中,我们讨论了针对周细胞在微血管功能障碍发展中的潜在作用以及参与调节周细胞活性以进行抗慢性排斥干预的分子途径。