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Am J Physiol Endocrinol Metab 293: E1296-E1302, 2007. First published August 21, 2007; doi:10.1152/ajpendo.00331.2007
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Myostatin regulates glucose uptake in BeWo cells

Nisha Antony,1 John J. Bass,1 Christopher D. McMahon,2,3 and Murray D. Mitchell1,2

1Liggins Institute, University of Auckland; 2National Research Centre for Growth and Development, Auckland; and 3Functional Muscle Genomics, AgResearch Limited, Ruakura Agricultural Centre, Hamilton, New Zealand

Submitted 27 May 2007 ; accepted in final form 11 August 2007

Myostatin is a member of the transforming growth factor (TGF)-beta superfamily, known for its ability to inhibit muscle growth. It can also regulate metabolism and glucose uptake in a number of tissues. To determine the mechanism of myostatin's effect on glucose uptake, we evaluated its actions using choriocarcinoma cell lines that are widely used as models for placental cells. Protein and mRNA were determined using immunoblotting and RT-PCR/PCR, respectively. Glucose uptake was assessed by uptake of radiolabeled deoxyglucose in vitro. All choriocarcinoma cell lines tested i.e., BeWo, JEG, and Jar, are used as models of placental cells, and all expressed myostatin protein and mRNA. Treatment of BeWo cells with myostatin resulted in inhibition of glucose uptake in a concentration-dependent manner (P < 0.01). At all concentrations tested, follistatin, a functional inhibitor of myostatin, completely blocked the inhibitory effect of myostatin (40 nM) on glucose uptake by BeWo cells (0.4 nM, P < 0.05). Follistatin treatment alone also increased glucose uptake (0.4 and 4 nM, P < 0.001; 40 nM, P < 0.05). Because BeWo cells proliferated and greater cell densities were achieved, glucose uptake declined irrespective of treatment. Myostatin treatment of BeWo cells did not alter the levels of myostatin receptor, ActRII A/B proteins. The levels of glucose transport proteins also remained unaltered in BeWo cells with myostatin treatment. This study has shown that myostatin specifically inhibits glucose uptake into BeWo cells, suggesting that locally produced myostatin may control glucose metabolism within the placenta.

myostatin; BeWo; placenta; glucose uptake; glucose transporter; glucose transporter; activin receptor; activin type II receptor A; activin type II receptor B; cell line; deoxyglucose



Address for reprint requests and other correspondence: M. D. Mitchell, Liggins Institute, Univ. of Auckland, Private Bag 92019, Auckland, New Zealand (e-mail: m.mitchell{at}auckland.ac.nz)




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