Coordinated expression of TNFα- and VEGF-mediated signaling components by placental macrophages in early and late pregnancy
Autor: | S.A. Selkov, O.V. Pavlov, A.V. Selutin, D. A. Niauri |
---|---|
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Adult Lipopolysaccharides Vascular Endothelial Growth Factor A medicine.medical_specialty medicine.medical_treatment Placenta Pregnancy Trimester Third Population Biology Receptors Tumor Necrosis Factor 03 medical and health sciences Young Adult 0302 clinical medicine Immune system Cell surface receptor Pregnancy Internal medicine medicine Humans Receptor education education.field_of_study 030219 obstetrics & reproductive medicine Tumor Necrosis Factor-alpha Macrophages Obstetrics and Gynecology Trophoblast Pregnancy Trimester First 030104 developmental biology medicine.anatomical_structure Cytokine Endocrinology Receptors Vascular Endothelial Growth Factor Reproductive Medicine Tumor necrosis factor alpha Female Developmental Biology Signal Transduction |
Zdroj: | Placenta. 42 |
ISSN: | 1532-3102 |
Popis: | Introduction Mononuclear phagocytes are thought to significantly contribute to cytokine regulation at the maternal-foetal interface, but the role of placental macrophages has been poorly investigated. TNFα and VEGF were demonstrated to have regulatory effects on basic structures of the placenta, particularly the trophoblast and blood vessels. The aims of this study were to determine the expression of TNFα, VEGF and related receptors in placental macrophages, and how does the participation of placental macrophages alter with gestational age in TNFα- and VEGF-mediated signaling. Methods Macrophages were isolated from placental villous tissue from normal pregnancies at either 9–12 or 38–40 weeks gestation. Cell surface receptors (TNFR1, TNFR2, VEGFR1, and VEGFR2) and intracellular TNFα and VEGF were quantified by flow cytometry after antibody staining. Basal and stimulated secretion of both cytokines and soluble TNF receptors was quantified by cytometric bead arrays. Secreted VEGFR1 was measured by ELISA. Results The expression of TNFR1 and VEGFR1 was remarkably variable and did not change from first to third trimester. There was minimal basal TNFα production in the placental macrophages, but nearly all cells in the population produced VEGF. TNFα and VEGF secretion increased with gestational age accompanied by decreased secretion of the antagonists sTNFR1 and sVEGFR. Macrophages isolated from early term placentas were less effective in responding to bacterial endotoxin. Lipopolysaccharide induced increases in the secretion of TNFα, TNFR1, TNFR2, and VEGFR1 but did not affect the production of VEGF. In late pregnancy, a significant correlation was observed between TNFR1 and VEGFR1. Discussion The progression of pregnancy is accompanied by the concerted increase in TNFα and VEGF secretion and decrease in the production of their soluble receptors, but the expression of cell surface receptors does not depend on gestational age. The observed patterns of basal and stimulated expression of TNFα and VEGF may reflect the dual immune and morphogenetic roles of placental macrophages in gestation. Compatible patterns of TNFR1 and VEGFR1 expression suggest common regulatory pathways for these receptors. |
Databáze: | OpenAIRE |
Externí odkaz: |