Melatonin and Leishmania amazonensis Infection Altered miR-294, miR-30e, and miR-302d Impacting on Tnf, Mcp-1, and Nos2 Expression
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | FERNANDES, Juliane Cristina Ribeiro | |
dc.contributor.author | AOKI, Juliana Ide | |
dc.contributor.author | ACUNA, Stephanie Maia | |
dc.contributor.author | ZAMPIERI, Ricardo Andrade | |
dc.contributor.author | MARKUS, Regina P. | |
dc.contributor.author | FLOETER-WINTER, Lucile Maria | |
dc.contributor.author | MUXEL, Sandra Marcia | |
dc.date.accessioned | 2019-05-30T13:57:47Z | |
dc.date.available | 2019-05-30T13:57:47Z | |
dc.date.issued | 2019 | |
dc.description.abstract | Leishmaniases are neglected diseases that cause a large spectrum of clinical manifestations, from cutaneous to visceral lesions. The initial steps of the inflammatory response involve the phagocytosis of Leishmania and the parasite replication inside the macrophage phagolysosome. Melatonin, the darkness-signaling hormone, is involved in modulation of macrophage activation during infectious diseases, controlling the inflammatory response against parasites. In this work, we showed that exogenous melatonin treatment of BALB/c macrophages reduced Leishmania amazonensis infection and modulated host microRNA (miRNA) expression profile, as well as cytokine production such as IL-6, MCP-1/CCL2, and, RANTES/CCL9. The role of one of the regulated miRNA (miR-294-3p) in L. amazonensis BALB/c infection was confirmed with miRNA inhibition assays, which led to increased expression levels of Tnf and Mcp-1/Ccl2 and diminished infectivity. Additionally, melatonin treatment or miR-30e-5p and miR-302d-3p inhibition increased nitric oxide synthase 2 (Nos2) mRNA expression levels and nitric oxide (NO) production, altering the macrophage activation state and reducing infection. Altogether, these data demonstrated the impact of melatonin treatment on the miRNA profile of BALB/c macrophage infected with L. amazonensis defining the infection outcome. | eng |
dc.description.index | MEDLINE | eng |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [479399/2012-3, 307587/2014-2, 406351/2018-0] | |
dc.description.sponsorship | Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2012/15263-4, 2014/50717-1, 2016/19815-2, 2016/03273-6, 2017/201906-9, 2017/23519-2] | |
dc.identifier.citation | FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, v.9, article ID 60, 15p, 2019 | |
dc.identifier.doi | 10.3389/fcimb.2019.00060 | |
dc.identifier.issn | 2235-2988 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/32030 | |
dc.language.iso | eng | |
dc.publisher | FRONTIERS MEDIA SA | eng |
dc.relation.ispartof | Frontiers in Cellular and Infection Microbiology | |
dc.rights | openAccess | eng |
dc.rights.holder | Copyright FRONTIERS MEDIA SA | eng |
dc.subject | polyamine pathway | eng |
dc.subject | nitric oxide synthase | eng |
dc.subject | arginase 1 | eng |
dc.subject | interleukin | eng |
dc.subject | mRNA-miRNA interaction | eng |
dc.subject | melatonin and Leishmania | eng |
dc.subject.other | nitric-oxide synthase | eng |
dc.subject.other | gene-expression | eng |
dc.subject.other | mice lacking | eng |
dc.subject.other | macrophage activation | eng |
dc.subject.other | murine macrophages | eng |
dc.subject.other | immune-responses | eng |
dc.subject.other | stromal cells | eng |
dc.subject.other | micrornas | eng |
dc.subject.other | induction | eng |
dc.subject.other | survival | eng |
dc.subject.wos | Immunology | eng |
dc.subject.wos | Microbiology | eng |
dc.title | Melatonin and Leishmania amazonensis Infection Altered miR-294, miR-30e, and miR-302d Impacting on Tnf, Mcp-1, and Nos2 Expression | eng |
dc.type | article | eng |
dc.type.category | original article | eng |
dc.type.version | publishedVersion | eng |
dspace.entity.type | Publication | |
hcfmusp.author.external | AOKI, Juliana Ide:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.author.external | ACUNA, Stephanie Maia:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.author.external | ZAMPIERI, Ricardo Andrade:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.author.external | MARKUS, Regina P.:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.author.external | FLOETER-WINTER, Lucile Maria:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.author.external | MUXEL, Sandra Marcia:Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil | |
hcfmusp.citation.scopus | 30 | |
hcfmusp.contributor.author-fmusphc | JULIANE CRISTINA RIBEIRO FERNANDES | |
hcfmusp.description.articlenumber | 60 | |
hcfmusp.description.volume | 9 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 30949455 | |
hcfmusp.origem.scopus | 2-s2.0-85064318107 | |
hcfmusp.origem.wos | WOS:000461821300002 | |
hcfmusp.publisher.city | LAUSANNE | eng |
hcfmusp.publisher.country | SWITZERLAND | eng |
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