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Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep

IGF-1 is a critical fetal growth-promoting hormone. Experimental infusion of an IGF-1 analog, human recombinant LR3 IGF-1, into late gestation fetal sheep increased fetal organ growth and skeletal muscle myoblast proliferation. However, LR3 IGF-1 has a low affinity for IGF binding proteins (IGFBP),...

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Autores principales: Stremming, J, White, A, Donthi, A, Batt, DG, Hetrick, B, Chang, EI, Wesolowski, SR, Seefeldt, MB, McCurdy, CE, Rozance, PJ, Brown, LD
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452821/
https://www.ncbi.nlm.nih.gov/pubmed/36091374
http://dx.doi.org/10.3389/fphys.2022.954948
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author Stremming, J
White, A
Donthi, A
Batt, DG
Hetrick, B
Chang, EI
Wesolowski, SR
Seefeldt, MB
McCurdy, CE
Rozance, PJ
Brown, LD
author_facet Stremming, J
White, A
Donthi, A
Batt, DG
Hetrick, B
Chang, EI
Wesolowski, SR
Seefeldt, MB
McCurdy, CE
Rozance, PJ
Brown, LD
author_sort Stremming, J
collection PubMed
description IGF-1 is a critical fetal growth-promoting hormone. Experimental infusion of an IGF-1 analog, human recombinant LR3 IGF-1, into late gestation fetal sheep increased fetal organ growth and skeletal muscle myoblast proliferation. However, LR3 IGF-1 has a low affinity for IGF binding proteins (IGFBP), thus reducing physiologic regulation of IGF-1 bioavailability. The peptide sequences for LR3 IGF-1 and sheep IGF-1 also differ. To overcome these limitations with LR3 IGF-1, we developed an ovine (sheep) specific recombinant IGF-1 (oIGF-1) and tested its effect on growth in fetal sheep. First, we measured in vitro myoblast proliferation in response to oIGF-1. Second, we examined anabolic signaling pathways from serial skeletal muscle biopsies in fetal sheep that received oIGF-1 or saline infusion for 2 hours. Finally, we measured the effect of fetal oIGF-1 infusion versus saline infusion (SAL) for 1 week on fetal body and organ growth, in vivo myoblast proliferation, skeletal muscle fractional protein synthetic rate, IGFBP expression in skeletal muscle and liver, and IGF-1 signaling pathways in skeletal muscle. Using this approach, we showed that oIGF-1 stimulated myoblast proliferation in vitro. When infused for 1 week, oIGF-1 increased organ growth of the heart, kidney, spleen, and adrenal glands and stimulated skeletal myoblast proliferation compared to SAL without increasing muscle fractional synthetic rate or hindlimb muscle mass. Hepatic and muscular gene expression of IGFBPs one to three was similar between oIGF-1 and SAL. We conclude that oIGF-1 promotes tissue and organ-specific growth in the normal sheep fetus.
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spelling pubmed-94528212022-09-09 Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep Stremming, J White, A Donthi, A Batt, DG Hetrick, B Chang, EI Wesolowski, SR Seefeldt, MB McCurdy, CE Rozance, PJ Brown, LD Front Physiol Physiology IGF-1 is a critical fetal growth-promoting hormone. Experimental infusion of an IGF-1 analog, human recombinant LR3 IGF-1, into late gestation fetal sheep increased fetal organ growth and skeletal muscle myoblast proliferation. However, LR3 IGF-1 has a low affinity for IGF binding proteins (IGFBP), thus reducing physiologic regulation of IGF-1 bioavailability. The peptide sequences for LR3 IGF-1 and sheep IGF-1 also differ. To overcome these limitations with LR3 IGF-1, we developed an ovine (sheep) specific recombinant IGF-1 (oIGF-1) and tested its effect on growth in fetal sheep. First, we measured in vitro myoblast proliferation in response to oIGF-1. Second, we examined anabolic signaling pathways from serial skeletal muscle biopsies in fetal sheep that received oIGF-1 or saline infusion for 2 hours. Finally, we measured the effect of fetal oIGF-1 infusion versus saline infusion (SAL) for 1 week on fetal body and organ growth, in vivo myoblast proliferation, skeletal muscle fractional protein synthetic rate, IGFBP expression in skeletal muscle and liver, and IGF-1 signaling pathways in skeletal muscle. Using this approach, we showed that oIGF-1 stimulated myoblast proliferation in vitro. When infused for 1 week, oIGF-1 increased organ growth of the heart, kidney, spleen, and adrenal glands and stimulated skeletal myoblast proliferation compared to SAL without increasing muscle fractional synthetic rate or hindlimb muscle mass. Hepatic and muscular gene expression of IGFBPs one to three was similar between oIGF-1 and SAL. We conclude that oIGF-1 promotes tissue and organ-specific growth in the normal sheep fetus. Frontiers Media S.A. 2022-08-25 /pmc/articles/PMC9452821/ /pubmed/36091374 http://dx.doi.org/10.3389/fphys.2022.954948 Text en Copyright © 2022 Stremming, White, Donthi, Batt, Hetrick, Chang, Wesolowski, Seefeldt, McCurdy, Rozance and Brown. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Stremming, J
White, A
Donthi, A
Batt, DG
Hetrick, B
Chang, EI
Wesolowski, SR
Seefeldt, MB
McCurdy, CE
Rozance, PJ
Brown, LD
Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title_full Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title_fullStr Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title_full_unstemmed Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title_short Sheep recombinant IGF-1 promotes organ-specific growth in fetal sheep
title_sort sheep recombinant igf-1 promotes organ-specific growth in fetal sheep
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452821/
https://www.ncbi.nlm.nih.gov/pubmed/36091374
http://dx.doi.org/10.3389/fphys.2022.954948
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