Targeting ATF4-DDIT4/TXNIP-Induced Ferroptosis: ISRIB as Novel Therapy for Septic Cardiomyopathy

Monday, March 23, 2026

2:30 PM - 3:30 PM Central Time

Location: Connections Central - RST 12

CY

Chen Yiting, N/A

China (People's Republic)

Disclosure(s): No relevant financial relationship(s) to disclose.
xW

xinrun Wang, n/a

China (People's Republic)

Disclosure(s): No relevant financial relationship(s) to disclose.
Jie Liu, N/A

Hunan, CHN

Disclosure(s): No relevant financial relationship(s) to disclose.
Jiyun Hu, N/A

CHN

Disclosure(s): No relevant financial relationship(s) to disclose.
GW

Guotao Wang, N/A

MD
Xiangya Hospital, Central South University

Disclosure information not submitted.
QH

Qihang Huang, N/A

MD
Xiangya Hospital, Central South University

Disclosure information not submitted.
ZQ

Zhaoxin Qian, n/a

MD, PhD
Xiangya Hospital Central South University

Disclosure information not submitted.
LZ

Lina Zhang, n/a

professor
Xiangya Hospital, Central South University, China (People's Republic)

Disclosure information not submitted.

Introduction: Sepsis-induced cardiomyopathy (SIC) is a reversible lesion in the early clinical stage, but often induces a high mortality rate in the late stage, and its specific mechanism is unknown. Thus, in-depth exploration of the biological progression mechanism of SIC plays a crucial role.

Methods: Through co-immunoprecipitation and molecular biological experiments, the functional interaction relationship between DDIT4 and TXNIP was clarified, and the effect of DDIT4/TXNIP on the progression of SIC was investigated both in vitro/vivo. Additionally, the mechanism of SIC cell death mediated by DDIT4/TXNIP was determined through PCR chip technology, Western blot, immunofluorescence, flow cytometry and in-vivo SIC model experiments. Finally, leveraging the upstream transcription factor ATF4 as a target for the DDIT4/TXNIP pathway, a novel application and translational study of its small-molecule inhibitor ISRIB in SIC was developed.

Results: Firstly, in-vitro/vivo experiments demonstrated that DDIT4 exacerbates inflammatory infiltration and cardiac dysfunction in SIC via the TXNIP pathway. Mechanistically, the DDIT4/TXNIP axis promotes SIC progression through ferroptosis mechanisms. Furthermore, our study identified ATF4, an upstream transcription factor of DDIT4/TXNIP, as a key regulatory switch for this biological mechanism. Finally, this study confirmed that ISRIB, a small-molecule inhibitor of ATF4, significantly suppresses inflammation and ferroptosis mediated by DDIT4/TXNIP, thereby markedly improving cardiac function and prognosis in SIC mice.

Conclusions: This study revealed that the DDIT4/TXNIP-mediated ferroptosis mechanism exacerbates the inflammatory release and cardiac function decline in SIC. It also clarified that this biological effect is regulated by ATF4. Moreover, it was proposed that the inhibitor ISRIB, which targets ATF4, can significantly attenuate ferroptosis in SIC, while concurrently protecting cardiac function. This finding provides a brand-new therapeutic target and intervention agent for the clinical treatment of SIC.