Hypoxia reduces expression and function of system A amino acid transporters in cultured term human trophoblasts

Author:

Nelson D. M.1,Smith S. D.1,Furesz T. C.2,Sadovsky Y.13,Ganapathy V.4,Parvin C. A.5,Smith C. H.2

Affiliation:

1. Department of Obstetrics and Gynecology,

2. Department of Pediatrics and St. Louis Children's Hospital, and Departments of

3. Cell Biology and Physiology and

4. Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, Georgia 30912-2100

5. Pathology, Washington University School of Medicine, St. Louis, Missouri 63110-1094; and

Abstract

We tested the hypothesis that hypoxia diminishes the expression and transport of neutral amino acids by system A in full-term human trophoblasts. Cytotrophoblasts from normal human placentas were cultured in standard conditions of 20% O2 or in 1% and 3% O2 for 24 h before assay. Neutral amino acid transport for systems A, ASC, and L was assayed at 24 and 72 h by the cluster-tray technique. Hypoxia during the initial 24 h of culture reduced system A transport by 82% in 1% O2 and by 37% in 3% O2 ( P < 0.01) compared with standard conditions. Hypoxia during the latter 24 h of the 72 h in culture reduced system A transport by 55% in 1% O2 and by 20% in 3% O2 ( P < 0.05) compared with standard conditions at 72 h. Hypoxia (1% O2) also reduced total amino acid transport by 40% in the more differentiated syncytiotrophoblasts present at 72 h. Northern analysis of trophoblasts in standard conditions showed that subtypes of human amino acid transporter A (hATA1 and hATA2) were each expressed in cytotrophoblasts and syncytiotrophoblasts. Hypoxia decreased expression of hATA1 and hATA2 in both trophoblast phenotypes. We conclude that hypoxia downregulates system A transporter expression and activity in cultured human trophoblasts.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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