Adipocyte‐specific Krüppel‐like factor 14 overexpression confers sex‐biased protection from weight gain on a high‐fat diet

Metabolic syndrome, a constellation of cardiometabolic risk factors including abdominal obesity, predisposes individuals to type 2 diabetes and cardiovascular disease. One frequently replicated MetSyn genetic association signal is located near KLF14 and is linked to central adiposity, with stronger effects observed in females. Lower KLF14 expression has been associated with detrimental metabolic phenotypes; however, the therapeutic effect of KLF14 germline overexpression remains unexplored. Here, we generated an adipocyte-specific Klf14 overexpression mouse model to investigate its role in metabolic regulation. Transgenic overexpression conferred sex-dependent metabolic benefits, including reduced weight gain, improved body composition, and enhanced acute insulin sensitivity, predominantly in female mice. These effects were accompanied by increased expression of genes involved in lipid uptake and thermogenic browning of white adipose tissue. Our findings demonstrate that KLF14 overexpression confers protective metabolic effects in a sex-specific manner and support the potential of KLF14-targeted strategies for treating metabolic syndrome.

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Publication Details

Journal
Physiological Reports
Published
2025-08-01
DOI
https://doi.org/10.14814/phy2.70513
Primary Topic
Kruppel-like factors research
Type
article
Field-Weighted Citation Impact
0.00

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article

Adipocyte‐specific Krüppel‐like factor 14 overexpression confers sex‐biased protection from weight gain on a high‐fat diet

Martha H. Thomas, Yonathan Tamrat Aberra, Mete Civelek, F S Keita et al.
Physiological Reports
Kruppel-like factors research
article

Adipocyte‐specific Krüppel‐like factor 14 overexpression confers sex‐biased protection from weight gain on a high‐fat diet

Martha H. Thomas, Yonathan Tamrat Aberra, Mete Civelek, F S Keita, Qianyi Yang, A. Cowan, Bilge Yaylak Gediksiz, David Gragirenes‐Delgado
article en

Abstract

Metabolic syndrome, a constellation of cardiometabolic risk factors including abdominal obesity, predisposes individuals to type 2 diabetes and cardiovascular disease. One frequently replicated MetSyn genetic association signal is located near KLF14 and is linked to central adiposity, with stronger effects observed in females. Lower KLF14 expression has been associated with detrimental metabolic phenotypes; however, the therapeutic effect of KLF14 germline overexpression remains unexplored. Here, we generated an adipocyte-specific Klf14 overexpression mouse model to investigate its role in metabolic regulation. Transgenic overexpression conferred sex-dependent metabolic benefits, including reduced weight gain, improved body composition, and enhanced acute insulin sensitivity, predominantly in female mice. These effects were accompanied by increased expression of genes involved in lipid uptake and thermogenic browning of white adipose tissue. Our findings demonstrate that KLF14 overexpression confers protective metabolic effects in a sex-specific manner and support the potential of KLF14-targeted strategies for treating metabolic syndrome.

Physiological ReportsVol. 13(15)
Howard University (US), University of Puerto Rico at Cayey (PR), University of Virginia (US)
National Science Foundation, American Diabetes Association, National Heart, Lung, and Blood Institute, Division of Diabetes, Endocrinology, and Metabolic Diseases
Good health and well-being
Openalex Percentile: Top 82%
Kruppel-like factors research
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