{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T14:19:32Z","timestamp":1784557172922,"version":"3.55.0"},"reference-count":75,"publisher":"Bioscientifica","issue":"3","content-domain":{"domain":["joe.bioscientifica.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2017,3]]},"abstract":"<jats:p>\n                    Adults who were affected by intrauterine growth restriction (IUGR) suffer from reductions in muscle mass and insulin resistance, suggesting muscle growth may be restricted by molecular events that occur during fetal development. To explore the basis of restricted fetal muscle growth, we used a sheep model of progressive placental insufficiency-induced IUGR to assess myoblast proliferation within intact skeletal muscle\n                    <jats:italic>in vivo<\/jats:italic>\n                    and isolated myoblasts stimulated with insulin\n                    <jats:italic>in vitro<\/jats:italic>\n                    . Gastrocnemius and soleus muscle weights were reduced by 25% in IUGR fetuses compared to those in controls (CON). The ratio of PAX7+ nuclei (a marker of myoblasts) to total nuclei was maintained in IUGR muscle compared to CON, but the fraction of PAX7+ myoblasts that also expressed Ki-67 (a marker of cellular proliferation) was reduced by 23%. Despite reduced proliferation\n                    <jats:italic>in vivo<\/jats:italic>\n                    , fetal myoblasts isolated from IUGR biceps femoris and cultured in enriched media\n                    <jats:italic>in vitro<\/jats:italic>\n                    responded robustly to insulin in a dose- and time-dependent manner to increase proliferation. Similarly, insulin stimulation of IUGR myoblasts upregulated key cell cycle genes and DNA replication. There were no differences in the expression of myogenic regulatory transcription factors that drive commitment to muscle differentiation between CON and IUGR groups. These results demonstrate that the molecular machinery necessary for transcriptional control of proliferation remains intact in IUGR fetal myoblasts, indicating that\n                    <jats:italic>in vivo<\/jats:italic>\n                    factors such as reduced insulin and IGF1, hypoxia and\/or elevated counter-regulatory hormones may be inhibiting muscle growth in IUGR fetuses.\n                  <\/jats:p>","DOI":"10.1530\/joe-16-0123","type":"journal-article","created":{"date-parts":[[2017,1,4]],"date-time":"2017-01-04T21:10:45Z","timestamp":1483564245000},"page":"475-491","update-policy":"https:\/\/doi.org\/10.1530\/crossmarkpolicy-5","source":"Crossref","is-referenced-by-count":37,"title":["Myoblast replication is reduced in the IUGR fetus despite maintained proliferative capacity in vitro"],"prefix":"10.1530","volume":"232","author":[{"given":"Susan M","family":"Soto","sequence":"first","affiliation":[{"name":"1Department of PediatricsUniversity of Colorado School of 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