scholarly journals Amino Acid (System A) Transporter Activity in Microvillous Membrane Vesicles from the Placentas of Appropriate and Small for Gestational Age Babies

1993 ◽  
Vol 34 (5) ◽  
pp. 661-665 ◽  
Author(s):  
Dhushy Maiiendran ◽  
Paul Donnai ◽  
Jocelyn D Glazier ◽  
Stephen W D'souza ◽  
Robert D H Boyd ◽  
...  
2012 ◽  
Vol 302 (2) ◽  
pp. E233-E242 ◽  
Author(s):  
Christina E. Hayward ◽  
Susan L. Greenwood ◽  
Colin P. Sibley ◽  
Philip N. Baker ◽  
John R. G. Challis ◽  
...  

Teenagers have an increased risk of delivering small-for-gestational-age (SGA) infants. Young maternal age and continued skeletal growth have been implicated as causal factors. In growing adolescent sheep, impaired placental development and nutrient transfer cause reduced birth weight. In human pregnancies, SGA is associated with reduced placental amino acid transport. Maternal growth has no effect on placental morphology or cell turnover, but growing teenagers have higher birth weight:placental weight ratios than nongrowing teenagers. We hypothesized that placental nutrient transporter activity would be affected by maternal age and/or growth status. Placentas from teenagers and adults were collected. Teenagers were defined as growing or nongrowing based on knee height measurements. System A amino acid transporter activity was quantified as sodium-dependent uptake of [14C]methylaminoisobutyric acid into placental fragments. Teenagers had lower placental system A activity than adults ( P < 0.05). In adults, placental system A activity was lower in SGA infants than appropriate-for-gestational-age (AGA) infants ( P < 0.05). In teenagers, AGA and SGA infants had lower placental system A activity than AGA infants born to adults ( P < 0.05). Placental system A activity was higher in growing teenagers than in nongrowing teenagers ( P < 0.001). Placental mRNA expression of system A transporter isoforms SLC38A1 and -2 was lower in teenagers than in adults ( P < 0.05) but did not differ between growing and nongrowing teenagers. There was no difference in transporter protein expression/localization between cohorts. Teenagers have inherently reduced placental transport, which may underlie their susceptibility to delivering SGA infants. Growing teenagers appear to overcome this susceptibility by stimulating the activity, but not expression, of system A transporters.


Placenta ◽  
2008 ◽  
Vol 29 (10) ◽  
pp. 879-882 ◽  
Author(s):  
E. Shibata ◽  
C.A. Hubel ◽  
R.W. Powers ◽  
F. von Versen-Hoeynck ◽  
H. Gammill ◽  
...  

2005 ◽  
Vol 24 (1) ◽  
pp. 65-74 ◽  
Author(s):  
Amanda Malina ◽  
Ashi Daftary ◽  
William Crombleholme ◽  
Nina Markovic ◽  
James M. Roberts

1988 ◽  
Vol 158 (1) ◽  
pp. 120-126 ◽  
Author(s):  
Irene Cetin ◽  
Anna M. Marconi ◽  
Patrizia Bozzetti ◽  
Lucia P. Sereni ◽  
Carlo Corbetta ◽  
...  

1991 ◽  
Vol 278 (1) ◽  
pp. 105-111 ◽  
Author(s):  
S Y Low ◽  
P M Taylor ◽  
A Ahmed ◽  
C I Pogson ◽  
M J Rennie

We investigated the effects of glutamine and histidine analogues on glutamine transport processes in membrane vesicles prepared from rat liver (sinusoidal membrane) and skeletal muscle (sarcolemma). L-[14C]Glutamine is transported in these membranes predominantly by Systems N/Nm (liver and muscle respectively), and to a lesser extent by Systems A and L (e.g. about 60, 20 and 20% of total flux respectively via Systems N, A and L at 0.05 mM-glutamine in liver membrane vesicles). The glutamine anti-metabolites 6-diazo-5-oxo-L-norleucine and acivicin were relatively poor inhibitors of glutamine uptake into liver membrane vesicles (less than 25% inhibition at 20-fold excess) and appeared primarily to inhibit System A activity (i.e. N-methylaminoisobutyric acid-inhibitable glutamine uptake). In similar experiments azaserine (also a glutamine anti-metabolite) inhibited approx. 50% of glutamine uptake, apparently by inhibition of System A and also of System L (i.e. 2-amino-2-carboxybicyclo[2,2,1]heptane-inhibitable glutamine uptake). Glutamate gamma-hydroxamate, aspartate beta-hydroxamate, histidine and N'-methylhistidine were all strong inhibitors of glutamine uptake into liver membrane vesicles (greater than 65% inhibition at 20-fold excess), but neither homoglutamine nor N'-methylhistidine produced inhibition. L-Glutamate-gamma-hydroxamate was shown to be a competitive inhibitor of glutamine transport via System N (Ki approximately 0.6 mM). Glutamine uptake in sarcolemmal vesicles showed a similar general pattern of inhibition as in liver membrane vesicles. The results highlight limits on the substrate tolerance of System N; we suggest that the presence of both an L-alpha-amino acid group and a nitrogen group with a delocalized lone-pair of electrons (amide or pyrrole type), separated by a specific intramolecular distance (C2-C4 chain equivalent), is important for substrate recognition by this transporter.


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