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

**Authors:** Yonathan Tamrat Aberra, Qianyi Yang, Ashlyn Cowan, Bilge Yaylak Gediksiz, Mitchell Thomas, David Gragirenes‐Delgado, Foday Keita, Mete Civelek

PMC · DOI: 10.14814/phy2.70513 · Physiological Reports · 2025-08-11

## TL;DR

Overexpression of KLF14 in fat cells protects female mice more than males from weight gain on a high-fat diet.

## Contribution

The study demonstrates sex-specific metabolic benefits of adipocyte-specific KLF14 overexpression in mice.

## Key findings

- Female mice with KLF14 overexpression showed reduced weight gain and improved body composition.
- KLF14 overexpression increased lipid uptake and thermogenic browning of white adipose tissue.
- Metabolic benefits were sex-dependent, with stronger effects observed in females.

## 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.

## Linked entities

- **Genes:** KLF14 (KLF transcription factor 14) [NCBI Gene 136259], KLF14 (KLF transcription factor 14) [NCBI Gene 136259]
- **Diseases:** Metabolic syndrome (MONDO:0000816), type 2 diabetes (MONDO:0005148), cardiovascular disease (MONDO:0004995)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Klf14 (Kruppel-like transcription factor 14) [NCBI Gene 619665] {aka 5330411L03Rik, BTEB5}
- **Diseases:** adiposity (MESH:D018205), Metabolic syndrome (MESH:D024821), cardiovascular disease (MESH:D002318), type 2 diabetes (MESH:D003924), weight gain (MESH:D015430), abdominal obesity (MESH:D056128)
- **Chemicals:** lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12339416/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12339416/full.md

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Source: https://tomesphere.com/paper/PMC12339416