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Published on: July 6, 2016
Cyclophilin A: a key player for etiological agent infection
Yating Liao1, Dan Luo1, Kailan Peng1
1Institute of Pathogenic Biology, Hengyang Medical College, University of South China, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, No. 28, West Changsheng Road, Hengyang City, 421001, Hunan Province, People's Republic of China.
Insights
Cyclophilin A (CypA) is crucial in viral, bacterial, and parasitic infections. CypA inhibitors show promise as host-targeting drugs against various infections and related diseases.
Area of Science:
- Immunology
- Virology
- Microbiology
- Pathology
Background:
- Cyclophilin A (CypA) is an abundant immunophilin involved in numerous cellular processes.
- CypA acts as an intracellular receptor for cyclosporine A and plays roles in various diseases.
- This review highlights CypA's multifaceted roles in infections caused by diverse etiological agents.
Purpose of the Study:
- To review the pivotal roles of Cyclophilin A (CypA) in infections.
- To explore CypA's interactions with viral, bacterial, and parasitic agents.
- To discuss the potential of CypA inhibitors as host-targeting therapeutic agents.
Main Methods:
- Literature review of studies on Cyclophilin A (CypA) and its involvement in infections.
- Analysis of CypA's interactions with viral proteins, bacterial toxins, and host cell structures.
- Summary of current research on CypA inhibitors as potential antiviral and anti-infective agents.
Main Results:
- CypA influences viral replication, often depending on host cell type and viral species.
- CypA is implicated in bacterial infections by regulating actin cytoskeleton, toxin translocation, and pathogen adhesion.
- CypA also impacts parasitic infections and host immune regulation.
Conclusions:
- CypA is a significant factor in the life cycle and pathogenesis of various infectious agents.
- CypA inhibitors demonstrate broad-spectrum antiviral activity and potential to overcome drug resistance.
- CypA inhibitors represent a promising host-targeting strategy for treating multiple infections and associated human diseases.
Abstract:
Cyclophilin A (CypA), a key member of the immunophilin family, is the most abundantly expressed isozyme of the 18 known human cyclophilins. Besides acting as an intracellular receptor for cyclosporine A, CypA plays a vital role in microorganismal infections, cardiovascular diseases, liver diseases, kidney diseases, neurodegeneration, cancer, rheumatoid arthritis, periodontitis, sepsis, asthma, and aging. This review focuses on the pivotal roles of CypA in the infection of etiological agents, which manifests mainly in promoting or inhibiting viral replication based on the host cell type and viral species. CypA can interact with viral proteins and thus regulate the replication cycle of the virus. CypA is involved in pathogenic bacterial infections by regulating the formation of host actin skeleton or membrane translocation of bacterial toxins, or mediated the adhesion of Mycoplasma genitalium during the infection processes by acting as a cellular receptor of M. genitalium. CypA also plays a critical role in infection or the life cycle of certain parasites or host immune regulation. Moreover, we summarized the current understanding of CypA inhibitors acting as host-targeting antiviral agents, thus opening an avenue for the treatment of multiple viral infections due to their broad antiviral effects and ability to effectively prevent drug resistance. Therefore, the antiviral effect of CypA has the potential to promote CypA inhibitors as host-targeting drugs to CypA-involved etiological agent infections and human diseases. KEY POINTS: • CypA is involved in the replication and infection of several viruses, pathogenic bacteria, mycoplasma, and parasites. • CypA inhibitors are in a strong position to inhibit the infection of viruses, bacterial, and mycoplasma.
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