Fator de necrose tumoral-alfa modula a migração celular trofoblástica via diminuição da expressão de aquaporina 3 em tecido placentário

Detalhes bibliográficos
Ano de defesa: 2020
Autor(a) principal: Passos Junior, Rinaldo Rodrigues dos
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Mato Grosso
Brasil
Instituto de Ciências Biológicas e da Saúde (ICBS) – Araguaia
UFMT CUA - Araguaia
Programa de Pós-Graduação em Imunologia e Parasitologia Básicas e Aplicadas
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://ri.ufmt.br/handle/1/5041
Resumo: Placentas from pre-eclamptic women display augmented tumor necrosis factor-alpha (TNF-α) levels simultaneously with reduced expression of aquaporin 3 (AQP3). However, whether TNF- α modulates AQP3 expression remains to be elucidated. We hypothesize that elevated levels of TNF-α, observed during hypertensive pregnancy, reduces AQP3 expression and negatively impact on trophoblastic cell migration. Spontaneously hypertensive rats (SHR) and Wistar (12- 14 wk) were divided into hypertensive and normotensive groups, respectively. In a third group, SHRs were treated with a TNF-α antagonist, etanercept (0.8 mg/kg, i.p.). Systolic blood pressure (SBP) was measured, and animals mated. Placentas were collected at 21 days of pregnancy. TNF-α (0, 5, 10 and 20 ng/mL,16 hours) was incubated with human placental explants, from normotensive pregnancies. Swan 71 cells were incubated with TNF-α (10 ng/mL) and subjected to the wound healing assay. AQP3 expression was assessed by western blot and TNF-α levels by ELISA. SBP (mmHg) was elevated in the hypertensive group, and etanercept treatment reduced this parameter. Placental TNF-α levels (pg/mL) were higher in the hypertensive group. AQP3 expression was reduced in the hypertensive group, and etanercept treatment reversed this parameter. Explants submitted to TNF-α exposition displayed reduced expression of AQP3. Trophoblastic cells incubated with TNF-α showed decreased cell migration and reduced AQP3 expression. Altogether, these data demonstrate that TNF-α negatively modulates AQP3 in placental tissue, impacting cell migration, and its relationship in a pregnancy affected by hypertensive conditions.