ABSTRACT
OBJECTIVE: We investigated the expression of heat shock protein 70 (Hsp70), nuclear factor of activated T cells 5 (NFAT5), and hypoxia-induced factor-1α (HIF-1α) in the placentas of normal and preeclamptic pregnancies and in human placental hypoxia models in vitro to examine the regulatory mechanisms of placental Hsp70 expression. METHODS: The expression levels of HIF-1α, NFAT5, and Hsp70 were examined in placental samples from 10 females with preeclampsia and 10 normotensive control patients and in human choriocarcinoma trophoblast cells treated with 1 mM CoCl2 by western blotting. Using models of placental hypoxia, pharmacological inhibition of HIF-1α with chetomin and shRNA knockdown and overexpression of NFAT5 were performed to investigate the roles of HIF-1α and NFAT5 in induction of Hsp70 by placental hypoxia. RESULTS: The levels of HIF-1α, NFAT5, and Hsp70 expression were significantly higher in the preeclamptic compared to normal placentas. In the placental hypoxia models, the expression of HIF-1α, NFAT5, and Hsp70 were significantly higher after 3, 6, and 12 h of 1 mM CoCl2 treatment, respectively. Pharmacological inhibition of HIF-1α suppressed the induction of NFAT5 and Hsp70 at the protein level. shRNA knockdown of NFAT5 suppressed the induction of Hsp70 protein and overexpression of NFAT5 stimulated the induction of Hsp70 mRNA and protein in models of human placental hypoxia in vitro. CONCLUSION: HIF-1α positively regulates the induction of NFAT5 and Hsp70 by placental hypoxia and NFAT5 stimulates transcription of Hsp70 in response to placental hypoxia in models of human placental hypoxia in vitro.
Subject(s)
HSP70 Heat-Shock Proteins/biosynthesis , Hypoxia/metabolism , Placenta/metabolism , Pre-Eclampsia/metabolism , Transcription Factors/biosynthesis , Cell Hypoxia , Cell Line, Tumor , Choriocarcinoma/metabolism , Cobalt , Disulfides/pharmacology , Female , Gene Knockdown Techniques , Humans , Hypoxia/chemically induced , Hypoxia-Inducible Factor 1, alpha Subunit/antagonists & inhibitors , Hypoxia-Inducible Factor 1, alpha Subunit/biosynthesis , In Vitro Techniques , Indole Alkaloids/pharmacology , Pregnancy , RNA, Small Interfering , Transcription Factors/geneticsABSTRACT
A simple and fast numerical method is developed capable of accurately determining the 3D rotational dynamics of a magnetic particle chain in an infinite fluid domain. The focus is to control the alternating breakup and reformation of the bead chain which we believe is essential to achieve effective fluid mixing at small scales. The numerical scheme makes use of magnetic dipole moments and extended forms of the Oseen-Burgers tensor to account for both the magnetic and hydrodynamic interactions between the particles. It is shown that the inclusion of hydrodynamic interaction between the particles is crucial to obtain a good description of the particle dynamics. Only a small error of deviation is observed when benchmarking the numerical scheme against a more computationally intensive method, the direct simulation method. The numerical results are compared with experiments and the simulated rotational dynamics correspond well with those obtained from video-microscopy experiments qualitatively and quantitatively. In addition, a dimensionless number (R(T)) is derived as the sole control parameter for the rotational bead chain dynamics. Numerically and experimentally, R(T)≈ 1 is the boundary between rigid "rod" and dynamic "breaking and reformation" behaviors.