Affiliation:
1. Laboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Universidade Federal de Pernambuco (UFPE), Avenida Prof. Moraes Rêgo 1235, Cidade Universitária, 50670-901 Recife, PE, Brazil
2. Laboratório de Glicoproteínas, Centro de Ciências Biológicas, Universidade Federal de Pernambuco (UFPE), Avenida Prof. Moraes Rêgo 1235, Cidade Universitária, 50670-901 Recife, PE, Brazil
Abstract
Cratylia mollislectin has already established cytokine induction in Th1 and Th2 pathways. Thereby, this study aimed to evaluate Cramoll 1, 4 in IL-6, IL-17A, IL-22, and IL-23 induction as well as analyze immunologic memory mechanism by reinducing lymphocyte stimulation. Initially we performed a screening in cultured splenocytes where Cramoll 1, 4 stimulated IL-6 production 5x more than ConA (P<0.05). The same behavior was observed with IL-22 where the increase was greater than 4x. Nevertheless, IL-17A induction was similar for both lectins. In PBMCs, the same splenocytes course was observed for IL-6 and IL-17A. Concerning the stimulation of IL-22 and IL-23 Cramoll 1, 4 was more efficient than ConA in cytokines stimulation mainly in IL-23 (P<0.01). Analyzing reinduced lymphocyte stimulation, IL-17A production was higher (P<0.001) when the first stimulus was realized with Cramoll 1, 4 at 1 μg/mL and the second at 5 μg/mL. IL-22 shows significant differences (P<0.01) at the same condition. Nevertheless, IL-23 revels the best response when the first stimuli was realized with Cramoll1, 4 at 100 ng/mL and the second with 5 μg/mL. We conclude that the Cramoll 1, 4 is able to induce IL-6, IL-17A, IL-22, and IL-23 cytokinesin vitrobetter than Concavalin A, besides immunologic memory generation, being a potential biotechnological tool in Th17 pathway studies.
Funder
Fundação de Amparo a Ciência and Tecnologia do Estado de Pernambuco (FACEPE)
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine
Cited by
12 articles.
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