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Hypoxia and Transforming Growth Factor-ß1 Act Independently to Increase Extracellular Matrix Production by Placental Fibroblasts

Division of High Risk Pregnancy (C.-P.C.), and Departments of Obstetrics and Gynecology (C.P.-C., Y.-C.Y., T.-H.S.) and Medical Research (C.-P.C., Y.-C.Y., C.-Y.C.), Mackay Memorial Hospital, Taipei 104, Taiwan; Mackay Medicine, Nursing and Management College (C.-P.C., Y.-C.Y., T.-H.S.), Taipei 112, Taiwan; and Academic Unit of Obstetrics and Gynaecology, Medical School (J.D.A.), University of Manchester, Manchester M13 0JH, United Kingdom

Address all correspondence and requests for reprints to: John D. Aplin, Ph.D., Research Floor, St. Mary’s Hospital, Manchester M13 0JH, United Kingdom. E-mail: John.Aplin{at}man.ac.uk.

Villous fibrosis is associated with oxygen deprivation in placental pathology, but the signaling networks and growth factors involved in activating the relevant cellular repair mechanisms are largely unknown. TGF is a powerful enhancer of extracellular matrix (ECM) production and an important immune suppressor that has been linked with fibrosis in several tissues. Here, cell culture methods were used to investigate possible links between hypoxia, elevated TGFß1, and altered ECM production in placenta. Term placental fibroblasts were isolated and cultured under hypoxia (3% O₂) or in the presence of TGFß1, and the expression of fibronectin, collagen I, and collagen IV was examined using immunohistochemistry, ELISA of cell monolayers with associated ECM, and real-time RT-PCR. The effect of hypoxia on endogenous production of TGFß1–3 was also examined. Both TGFß1 and hypoxia increased fibronectin, collagen I, and collagen IV protein and mRNA in placental fibroblasts. However, TGFß1–3 production was not increased by culturing the cells under hypoxic conditions for 5 d. Thus, increased ECM expression under hypoxia was not mediated directly by increased TGFß. We conclude that ECM production can be stimulated independently by hypoxia and TGFß1.

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