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The Complement System, Aging, and Aging-Related Diseases

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Aug 12
PMID 35955822
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Abstract

The complement system is a part of the immune system and consists of multiple complement components with biological functions such as defense against pathogens and immunomodulation. The complement system has three activation pathways: the classical pathway, the lectin pathway, and the alternative pathway. Increasing evidence indicates that the complement system plays a role in aging. Complement plays a role in inflammatory processes, metabolism, apoptosis, mitochondrial function, and Wnt signaling pathways. In addition, the complement system plays a significant role in aging-related diseases, including Alzheimer's disease, age-related macular degeneration, and osteoarthritis. However, the effect of complement on aging and aging-related diseases is still unclear. Thus, a better understanding of the potential relationship between complement, aging, and aging-related diseases will provide molecular targets for treating aging, while focusing on the balance of complement in during treatment. Inhibition of a single component does not result in a good outcome. In this review, we discussed the research progress and effects of complement in aging and aging-related diseases.

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References
1.
Dodig S, cepelak I, Pavic I . Hallmarks of senescence and aging. Biochem Med (Zagreb). 2019; 29(3):030501. PMC: 6610675. DOI: 10.11613/BM.2019.030501. View

2.
Al-Sofiani M, Ganji S, Kalyani R . Body composition changes in diabetes and aging. J Diabetes Complications. 2019; 33(6):451-459. PMC: 6690191. DOI: 10.1016/j.jdiacomp.2019.03.007. View

3.
Franceschi C, Campisi J . Chronic inflammation (inflammaging) and its potential contribution to age-associated diseases. J Gerontol A Biol Sci Med Sci. 2014; 69 Suppl 1:S4-9. DOI: 10.1093/gerona/glu057. View

4.
Hoppel C, Lesnefsky E, Chen Q, Tandler B . Mitochondrial Dysfunction in Cardiovascular Aging. Adv Exp Med Biol. 2017; 982:451-464. DOI: 10.1007/978-3-319-55330-6_24. View

5.
Schafer N, Grassel S . Involvement of complement peptides C3a and C5a in osteoarthritis pathology. Peptides. 2022; 154:170815. DOI: 10.1016/j.peptides.2022.170815. View