| Literature DB >> 33498417 |
Malgorzata Kloc1,2,3, Ahmed Uosef1,2, Martha Villagran4,5, Robert Zdanowski6, Jacek Z Kubiak7,8, Jarek Wosik4,5, Rafik M Ghobrial1,2.
Abstract
The small GTPase RhoA, and its down-stream effector ROCK kinase, and the interacting Rac1and and mTORC2 pathways, are the principal regulators of the actin cytoskeleton and actin-related functions in all eukaryotic cells, including the immune cells. As such, they also regulate the phenotypes and functions of macrophages in the immune response and beyond. Here, we review the results of our and other's studies on the role of the actin and RhoA pathway in shaping the macrophage functions in general and macrophage immune response during the development of chronic (long term) rejection of allografts in the rodent cardiac transplantation model. We focus on the importance of timing of the macrophage functions in chronic rejection and how the circadian rhythm may affect the anti-chronic rejection therapies.Entities:
Keywords: ROCK; Rac1; RhoA; actin; chronic rejection; circadian rhythm; macrophage; mouse; rat; timing; transplantation
Year: 2021 PMID: 33498417 DOI: 10.3390/biology10020070
Source DB: PubMed Journal: Biology (Basel) ISSN: 2079-7737