Caracterização biológica e molecular de tripomastigotas de Trypanosoma cruzi provenientes de células deficientes na proteína lisossomal LAMP

• Ano de defesa: 2021
• Autor(a) principal: Anny Carolline Silva Oliveira
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Minas Gerais; Brasil; ICB - DEPARTAMENTO DE MORFOLOGIA; Programa de Pós-Graduação em Biologia Celular; UFMG
• Palavras-chave em Português: Trypanosoma cruzi; Doença de Chagas; Proteínas LAMP; Invasão; Ambiente intracelular; Análise proteômica; TMT (tandem mass tags); Biologia celular; Tryoanosoma cruzi; Espaço intracelular; Glicoproteínas de membrana associadas ao lisossomo
• Link de acesso: http://hdl.handle.net/1843/51245

Trypanosoma cruzi invades non-professional phagocytic cells by subverting their membrane repair process, which is dependent on membrane injury and cell signaling, intracellular calcium increase and lysosome recruitment. Cells lacking Lysosome Associated Membrane Proteins 1 and 2 (LAMP-1 and LAMP-2) are less permissive to parasite invasion, however more prone to parasite intracellular multiplication. Several passages through a different intracellular environment can significantly change T. cruzi’s gene expression profile. Here, we evaluated whether one single passage through LAMP deficient (KO) or wild type (WT) fibroblasts could influence invasion ability of T. cruzi Y strain trypomastigotes in L6 myoblasts and WT fibroblasts. Parasites released from LAMP-2 KO cells (TcY-L2-/-) showed higher invasion, calcium signaling and membrane injury rates when compared to those released from WT (TcY-WT) or LAMP-1/2 KO cells (TcY-L1/2-/-) in L6 myoblasts. On the other hand, TcY-L1/2-/- showed higher invasion, calcium signaling and cell membrane injury rates compared to the others in WT fibroblasts. TcY-WT, on the other hand, although presented an intermediary invasion and calcium signaling rates in WT cells, induced lower levels of injury, reinforcing that protein signaling also have a significant contribution to parasite induced calcium signals. These results clearly show that parasites released from WT or LAMP KO cells are distinct from each other. Additionally, these parasites ability to invade the cell may be distinct depending with which cell type they interact with. Since these alterations most likely would reflect differences among parasite surface molecules, we also evaluated their subproteome. Few protein complexes, membrane and secreted proteins were found regulated, such as some members of MASP, mucins, trans-sialidases and gp63 proteins family, which may play an important role during parasite infection.