| Literature DB >> 31310832 |
Thaise L Teixeira1, Patrícia Castilhos1, Cassiano C Rodrigues1, Aline A da Silva1, Rebecca Ts Brígido1, Samuel C Teixeira1, Bruna C Borges1, Marlus A Dos Santos1, Flávia A Martins1, Paulo César F Santos2, João Paulo S Servato3, M S Silva4, M J B da Silva5, M C Elias4, Claudio V da Silva6.
Abstract
P21 is a protein secreted by Trypanosoma cruzi (T. cruzi). Previous studies have shown a spectrum of biological activities performed by P21 such as induction of phagocytosis, leukocyte chemotaxis and inhibition of angiogenesis. However, the activity of P21 in T. cruzi infection remains unknown. Here, we reported the role of P21 in mice harboring late T. cruzi infection. Treatment with recombinant P21 protein (rP21) reduced parasite load and angiogenesis, and induced fibrosis in the cardiac tissue of infected mice. In addition, rP21 reduced the growth of epimastigotes, inhibited intracellular replication of amastigotes and modulated the parasite cell cycle. Our data suggest that P21 controls parasite replication in the host, supporting the survival of both parasite and host.Entities:
Keywords: Angiogenesis; Chagas disease; Fibrosis; Intracellular replication; Life cycle; P21 protein
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Year: 2019 PMID: 31310832 DOI: 10.1016/j.micpath.2019.103618
Source DB: PubMed Journal: Microb Pathog ISSN: 0882-4010 Impact factor: 3.738