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GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue
INTRODUCTION: Adipokines are proteins that are secreted by the adipose tissue. Although they are associated with obesity-related metabolic disorders, most studies have focused on adipokines expressed by visceral adipose tissue (VAT). This study aimed to identify the adipokine potentially derived fro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390302/ https://www.ncbi.nlm.nih.gov/pubmed/37529611 http://dx.doi.org/10.3389/fendo.2023.1159515 |
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author | Song, Mi Kyung Kim, Ji Eun Kim, Jung Tae Kang, Yea Eun Han, Sun Jong Kim, Seok Hwan Kim, Hyun Jin Ku, Bon Jeong Lee, Ju Hee |
author_facet | Song, Mi Kyung Kim, Ji Eun Kim, Jung Tae Kang, Yea Eun Han, Sun Jong Kim, Seok Hwan Kim, Hyun Jin Ku, Bon Jeong Lee, Ju Hee |
author_sort | Song, Mi Kyung |
collection | PubMed |
description | INTRODUCTION: Adipokines are proteins that are secreted by the adipose tissue. Although they are associated with obesity-related metabolic disorders, most studies have focused on adipokines expressed by visceral adipose tissue (VAT). This study aimed to identify the adipokine potentially derived from subcutaneous adipose tissue (SAT) and its clinical significance. METHODS: Samples of SAT and VAT were obtained from six adult male patients who underwent laparoscopic surgery for benign gall bladder disease. Differentially expressed genes were analyzed by subjecting the samples to RNA sequencing. The serum concentration of selected proteins according to body mass index (BMI) was analyzed in 58 individuals. RESULTS: GDF10 showed significantly higher expression in the SAT, as per RNA sequencing (fold change = 5.8, adjusted P value = 0.009). Genes related to insulin response, glucose homeostasis, lipid homeostasis, and fatty acid metabolism were suppressed when GDF10 expression was high in SAT, as per genotype-tissue expression data. The serum GDF10 concentration was higher in participants with BMI ≥ 25 kg/m(2) (n = 35, 2674 ± 441 pg/mL) than in those with BMI < 25 kg/m(2) (n = 23, 2339 ± 639 pg/mL; P = 0.022). There was a positive correlation between BMI and serum GDF10 concentration (r = 0.308, P = 0.019). CONCLUSIONS: GDF10 expression was higher in SAT than in VAT. Serum GDF10 concentration was high in patients with obesity. Therefore, GDF10 could be a SAT-derived protein related to obesity. |
format | Online Article Text |
id | pubmed-10390302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103903022023-08-01 GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue Song, Mi Kyung Kim, Ji Eun Kim, Jung Tae Kang, Yea Eun Han, Sun Jong Kim, Seok Hwan Kim, Hyun Jin Ku, Bon Jeong Lee, Ju Hee Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: Adipokines are proteins that are secreted by the adipose tissue. Although they are associated with obesity-related metabolic disorders, most studies have focused on adipokines expressed by visceral adipose tissue (VAT). This study aimed to identify the adipokine potentially derived from subcutaneous adipose tissue (SAT) and its clinical significance. METHODS: Samples of SAT and VAT were obtained from six adult male patients who underwent laparoscopic surgery for benign gall bladder disease. Differentially expressed genes were analyzed by subjecting the samples to RNA sequencing. The serum concentration of selected proteins according to body mass index (BMI) was analyzed in 58 individuals. RESULTS: GDF10 showed significantly higher expression in the SAT, as per RNA sequencing (fold change = 5.8, adjusted P value = 0.009). Genes related to insulin response, glucose homeostasis, lipid homeostasis, and fatty acid metabolism were suppressed when GDF10 expression was high in SAT, as per genotype-tissue expression data. The serum GDF10 concentration was higher in participants with BMI ≥ 25 kg/m(2) (n = 35, 2674 ± 441 pg/mL) than in those with BMI < 25 kg/m(2) (n = 23, 2339 ± 639 pg/mL; P = 0.022). There was a positive correlation between BMI and serum GDF10 concentration (r = 0.308, P = 0.019). CONCLUSIONS: GDF10 expression was higher in SAT than in VAT. Serum GDF10 concentration was high in patients with obesity. Therefore, GDF10 could be a SAT-derived protein related to obesity. Frontiers Media S.A. 2023-07-14 /pmc/articles/PMC10390302/ /pubmed/37529611 http://dx.doi.org/10.3389/fendo.2023.1159515 Text en Copyright © 2023 Song, Kim, Kim, Kang, Han, Kim, Kim, Ku and Lee 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 | Endocrinology Song, Mi Kyung Kim, Ji Eun Kim, Jung Tae Kang, Yea Eun Han, Sun Jong Kim, Seok Hwan Kim, Hyun Jin Ku, Bon Jeong Lee, Ju Hee GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title | GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title_full | GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title_fullStr | GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title_full_unstemmed | GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title_short | GDF10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
title_sort | gdf10 is related to obesity as an adipokine derived from subcutaneous adipose tissue |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390302/ https://www.ncbi.nlm.nih.gov/pubmed/37529611 http://dx.doi.org/10.3389/fendo.2023.1159515 |
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