| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
RESEARCH |
1 Maternal-Fetal Physiology, Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, UK, 2 Animal Breeding and Development, Scottish Agricultural College, Aberdeen AB21 9YA, UK and 3 College of Life Science and Medicine, University of Aberdeen, Aberdeen AB25 2ZD, UK
Correspondence should be addressed to H J McArdle; Email: H.McArdle{at}rowett.ac.uk
Trans-placental transport of amino acids is vital for the developing fetus. Using the BeWo cell line as a placental model, we investigated the effect of restricting amino acid availability on amino acid transport system type A. BeWo cells were cultured either in amino acid-depleted (without non-essential amino acids) or control media for 1, 3, 5 or 6 h. System A function was analysed using
(methyl-amino)isobutyric acid (MeAIB) transcellular transport studies. Transporter (sodium coupled neutral amino acid transporter (SNAT1/2)) expression was analysed at mRNA and protein level by Northern and Western blotting respectively. Localisation was carried out using immunocytochemistry. MeAIB transcellular transport was significantly (P < 0.05) increased by incubation of the cells in amino acid-depleted medium for 1 h, and longer incubation times caused further increases in the rate of transfer. However, the initial response was not accompanied by an increase in SNAT2 mRNA; this occurred only after 3 h and further increased for the rest of the 6-h incubation. Similarly, it took several hours for a significant increase in SNAT2 protein expression. In contrast, relocalisation of existing SNAT2 transporters occurred within 30 min of amino acid restriction and continued throughout the 6-h incubation. When the cells were incubated in medium with even lower amino acid levels (without non-essential plus 0.5 x essential amino acids), SNAT2 mRNA levels showed further significant (P < 0.0001) up-regulation. However, incubation of cells in depleted medium for 6 h caused a significant (P = 0.014) decrease in the expression of SNAT1 mRNA. System L type amino acid transporter 2 (LAT2) expression was not changed by amino acid restriction, indicating that the responses seen in the system A transporters were not a general cell response. These data have shown that placental cells adapt in vitro to nutritional stress and have identified the physiological, biochemical and genomic mechanisms involved.
This article has been cited by other articles:
![]() |
M. Snook Parrott, F. von Versen-Hoeynck, R. B. Ness, N. Markovic, and J. M. Roberts System A Amino Acid Transporter Activity in Term Placenta Is Substrate Specific and Inversely Related to Amino Acid Concentration Reproductive Sciences, October 1, 2007; 14(7): 687 - 693. [Abstract] [PDF] |
||||
![]() |
J. J. Eckert, F. D. Houghton, J. A. Hawkhead, A. H. Balen, H. J. Leese, H. M. Picton, I. T. Cameron, and T. P. Fleming Human embryos developing in vitro are susceptible to impaired epithelial junction biogenesis correlating with abnormal metabolic activity Hum. Reprod., August 1, 2007; 22(8): 2214 - 2224. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Jansson, J. Pettersson, A. Haafiz, A. Ericsson, I. Palmberg, M. Tranberg, V. Ganapathy, T. L. Powell, and T. Jansson Down-regulation of placental transport of amino acids precedes the development of intrauterine growth restriction in rats fed a low protein diet J. Physiol., November 1, 2006; 576(3): 935 - 946. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |