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.
| Original language | English (US) |
|---|---|
| Article number | 70 |
| Pages (from-to) | 1-16 |
| Number of pages | 16 |
| Journal | Biology |
| Volume | 10 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 20 2021 |
Keywords
- Actin
- Chronic rejection
- Circadian rhythm
- Macrophage
- Mouse
- ROCK
- Rac1
- Rat
- RhoA
- Timing
- Transplantation
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology
- General Immunology and Microbiology
- General Agricultural and Biological Sciences
Divisions
- Abdominal Transplant
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