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      Rates of myogenesis and myofiber numbers are reduced in late gestation IUGR fetal sheep

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          Abstract

          Intrauterine growth restricted (IUGR) fetuses are born with reduced skeletal muscle mass. We hypothesized that reduced rates of myogenesis would contribute to fewer and smaller myofibers in IUGR fetal hindlimb muscle compared to the normally growing fetus. We tested this hypothesis in IUGR fetal sheep with progressive placental insufficiency produced by exposing pregnant ewes to elevated ambient temperatures from 38 to 116 days gestation (dGA; term=147 dGA). Surgically catheterized control (CON, n=8) and IUGR (n=13) fetal sheep were injected with intravenous 5-bromo-2’-deoxyuridine (BrdU) prior to muscle collection (134 dGA). Rates of myogenesis, defined as the combined processes of myoblast proliferation, differentiation, and fusion into myofibers, were determined in biceps femoris (BF), tibialis anterior (TA), and flexor digitorum superficialis (FDS) muscles. Total myofiber number was determined for the entire cross-section of the FDS muscle. In IUGR fetuses, the number of BrdU + myonuclei per myofiber cross-section was lower in BF, TA, and FDS ( P<0.05), total myonuclear number per myofiber cross-section was lower in BF and FDS ( P<0.05), and total myofiber number was lower in FDS ( P<0.005) compared to CON. mRNA expression levels of cyclins, cyclin dependent protein kinases, and myogenic regulatory factors were lower ( P<0.05), and inhibitors of the cell cycle were higher ( P<0.05) in IUGR BF compared to CON. Markers of apoptosis were not different in IUGR BF muscle. These results show that in IUGR fetuses, reduced rates of myogenesis produce fewer numbers of myonuclei, which may limit hypertrophic myofiber growth. Fewer myofibers of smaller size contribute to smaller muscle mass in the IUGR fetus.

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          Author and article information

          Journal
          0375363
          4713
          J Endocrinol
          J. Endocrinol.
          The Journal of endocrinology
          0022-0795
          1479-6805
          11 December 2019
          19 December 2019
          19 December 2019
          19 December 2020
          : 244
          : 2
          : 339-352
          Affiliations
          [1 ]Department of Pediatrics, University of Colorado School of Medicine, Perinatal Research Center, Aurora, Colorado, USA.
          [2 ]Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, Colorado, USA.
          [3 ]Department of Molecular, Cellular and Developmental Biology and BioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado, USA.
          Author notes
          Corresponding author (and to whom reprint requests should be addressed): Laura D. Brown, MD, Perinatal Research Center, 13243 E 23 rd Avenue, MS F441, Aurora, CO 80045, Phone: 303-724-0106, Fax: 303-724-0898, Laura.Brown@ 123456ucdenver.edu
          Article
          PMC7192794 PMC7192794 7192794 nihpa1544962
          10.1530/JOE-19-0273
          7192794
          31751294
          535db9a5-bd1c-42a2-91da-3dd70c03921f
          History
          Categories
          Article

          fetal programming,myonuclear domain,myoblast,myogenesis,skeletal muscle

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