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The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals

AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene a...

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Autores principales: Høyer, Katrine L., Høgild, Morten L., List, Edward O., Lee, Kevin Y., Kissinger, Emily, Sharma, Rita, Erik Magnusson, Nils, Puri, Vishwajeet, Kopchick, John J., Jørgensen, Jens O. L., Jessen, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029434/
https://www.ncbi.nlm.nih.gov/pubmed/32073221
http://dx.doi.org/10.14814/phy2.14373
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author Høyer, Katrine L.
Høgild, Morten L.
List, Edward O.
Lee, Kevin Y.
Kissinger, Emily
Sharma, Rita
Erik Magnusson, Nils
Puri, Vishwajeet
Kopchick, John J.
Jørgensen, Jens O. L.
Jessen, Niels
author_facet Høyer, Katrine L.
Høgild, Morten L.
List, Edward O.
Lee, Kevin Y.
Kissinger, Emily
Sharma, Rita
Erik Magnusson, Nils
Puri, Vishwajeet
Kopchick, John J.
Jørgensen, Jens O. L.
Jessen, Niels
author_sort Høyer, Katrine L.
collection PubMed
description AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30–120 min. Human data were corroborated in adipose‐specific GH receptor knockout (FaGHRKO) mice versus wild‐type mice. Expression of candidate genes identified in the array were investigated in 3T3‐L1 adipocytes. RESULTS: GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild‐type mice, but not in FaGHRKO mice. The array identified 53 GH‐regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin‐dependent antilipolytic signal, upregulation of PTEN that inhibits insulin‐dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3‐L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2. CONCLUSION: (a) GH directly stimulates AT lipolysis in a GHR‐dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined.
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spelling pubmed-70294342020-02-19 The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals Høyer, Katrine L. Høgild, Morten L. List, Edward O. Lee, Kevin Y. Kissinger, Emily Sharma, Rita Erik Magnusson, Nils Puri, Vishwajeet Kopchick, John J. Jørgensen, Jens O. L. Jessen, Niels Physiol Rep Original Research AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30–120 min. Human data were corroborated in adipose‐specific GH receptor knockout (FaGHRKO) mice versus wild‐type mice. Expression of candidate genes identified in the array were investigated in 3T3‐L1 adipocytes. RESULTS: GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild‐type mice, but not in FaGHRKO mice. The array identified 53 GH‐regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin‐dependent antilipolytic signal, upregulation of PTEN that inhibits insulin‐dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3‐L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2. CONCLUSION: (a) GH directly stimulates AT lipolysis in a GHR‐dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined. John Wiley and Sons Inc. 2020-02-19 /pmc/articles/PMC7029434/ /pubmed/32073221 http://dx.doi.org/10.14814/phy2.14373 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Høyer, Katrine L.
Høgild, Morten L.
List, Edward O.
Lee, Kevin Y.
Kissinger, Emily
Sharma, Rita
Erik Magnusson, Nils
Puri, Vishwajeet
Kopchick, John J.
Jørgensen, Jens O. L.
Jessen, Niels
The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title_full The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title_fullStr The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title_full_unstemmed The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title_short The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
title_sort acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029434/
https://www.ncbi.nlm.nih.gov/pubmed/32073221
http://dx.doi.org/10.14814/phy2.14373
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