# Overexpression of GDF15 protects kidneys from ischemia reperfusion injury and affects circular RNA expression

**Authors:** Cuilin Zhu, Qing Liu, Yale Su, Yixin Zhang, Aanal Patel, Adam Greasley, Jifu Jiang, Douglas Quan, Weiping Min, Kexiang Liu, Xiufen Zheng

PMC · DOI: 10.3389/fcell.2025.1577625 · Frontiers in Cell and Developmental Biology · 2025-07-02

## TL;DR

Overexpression of GDF15 protects kidneys from injury and reduces cell death and inflammation in a mouse model of renal failure.

## Contribution

This study demonstrates that GDF15 overexpression reduces kidney damage and alters circular RNA expression in ischemia reperfusion injury.

## Key findings

- GDF15 overexpression reduces mortality and improves kidney function in mice with renal IRI.
- GDF15 decreases apoptosis, inflammation, and pathological changes in injured kidneys.
- GDF15 modulates the expression of specific circular RNAs like Smad3, Hipk3, and Crim1.

## Abstract

Renal failure and dysfunction remain one of the most significant morbidities impacting patient’s life. Effective treatments still lack in the context of an increasing number of patients with renal failure. This study aims to investigate the impact of growth differentiation factor 15 (GDF15) in treating renal dysfunction and to explore its therapeutic potential.

Renal injury was induced with a murine ischemia reperfusion injury (IRI) model. Mice overexpressing GDF15 (GDF15 transgenic (GDF15TG) mice, GDF15 knock out (GDF15 KO) mice and wild type (WT) mice all underwent IRI to test the effects of GDF15 on renal injury. Renal function and histopathological changes were measured 24 h after reperfusion. Cell apoptosis was detected by TUNEL and tissue inflammation was detected by myeloperoxidase (MPO) activity. qRT-PCR was conducted to determine the expression of genes and circular RNAs.

Overexpression of GDF15 reduced mortality of mice with lethal renal IRI whereas GDF15 deficiency increased the mortality. GDF15TG mice had better renal function with the lower levels of blood creatinine and blood urea nitrogen (BUN). Over-expression of GDF15 reduced kidney pathological changes, cell apoptosis, neutrophil infiltration and mortality. Over-expression of GDF15 also decreased the expression of apoptotic genes (high mobility group 1, HMGA1 and Bax), inflammatory genes IL-1β, IL-6, tumor necrosis factor (TNF-α), chemokine 1 (CK1), and senescent gene p21 whereas increases Bcl-XL, Importin 11 and CRIM1. IRI upregulated circular RNA Smad3 and reduced circular RNA Hipk3 and circular RNA Crim1, which was offset by GDF15.

Over-expression of GDF15 protects renal function and prevents renal failure, highlighting its potential in treating renal failure.

## Linked entities

- **Genes:** GDF15 (growth differentiation factor 15) [NCBI Gene 9518], HMGA1 (high mobility group AT-hook 1) [NCBI Gene 3159], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], IL1B (interleukin 1 beta) [NCBI Gene 3553], IL6 (interleukin 6) [NCBI Gene 3569], TNF (tumor necrosis factor) [NCBI Gene 7124], CSNK1A1 (casein kinase 1 alpha 1) [NCBI Gene 1452], CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026], Bcl2l1 (BCL2-like 1) [NCBI Gene 12048], CRIM1 (cysteine rich transmembrane BMP regulator 1) [NCBI Gene 51232], SMAD3 (SMAD family member 3) [NCBI Gene 4088], HIPK3 (homeodomain interacting protein kinase 3) [NCBI Gene 10114], CRIM1 (cysteine rich transmembrane BMP regulator 1) [NCBI Gene 51232]
- **Diseases:** renal failure (MONDO:0001106)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Bcl2l1 (BCL2-like 1) [NCBI Gene 12048] {aka Bcl(X)L, Bcl-XL, Bcl2l, BclX, bcl-x, bcl2-L-1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Smad3 (SMAD family member 3) [NCBI Gene 17127] {aka Madh3}, Gdf15 (growth differentiation factor 15) [NCBI Gene 23886] {aka MIC-1, NAG-1, SBF}, Hmga1 (high mobility group AT-hook 1) [NCBI Gene 15361] {aka Hmga1a, Hmga1b, Hmgi, Hmgiy, Hmgy}, Hipk3 (homeodomain interacting protein kinase 3) [NCBI Gene 15259] {aka DYRK6, FIST3, PKY, mir-1902}, Cdkn1a (cyclin dependent kinase inhibitor 1A) [NCBI Gene 12575] {aka CAP20, CDKI, CIP1, Cdkn1, P21, SDI1}, Bax (BCL2-associated X protein) [NCBI Gene 12028], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Ipo11 (importin 11) [NCBI Gene 76582] {aka 1700081H05Rik, 2510001A17Rik, E330021B14Rik, Ranbp11}, Crim1 (cysteine rich transmembrane BMP regulator 1) [NCBI Gene 50766], Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Diseases:** Renal failure and dysfunction (MESH:D051437), IRI (MESH:D015427), inflammation (MESH:D007249), Renal injury (MESH:D007674), renal IRI (MESH:D007511)
- **Chemicals:** creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12263956/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12263956/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12263956/full.md

---
Source: https://tomesphere.com/paper/PMC12263956