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Pyruvate Regulates the Expression of DLAT to Promote Follicular Growth
Journal article   Open access   Peer reviewed

Pyruvate Regulates the Expression of DLAT to Promote Follicular Growth

Liuhong Zhang, Yixuan Guo, Enyuan Huang, Jianing Lu, Tiantian Wang, Yonghua Shi, Meng Lv, Yongcai Chen, Shuo Li, Xiaolong Yuan, …
Cells (Basel, Switzerland), Vol.14(6), 444
2025
PMID: 40136693
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Published4.68 MBDownloadView
CC BY V4.0 Open Access

Abstract

Animals Apoptosis - drug effects Apoptosis - genetics Cell Proliferation - drug effects Dihydrolipoyllysine-Residue Acetyltransferase - genetics Dihydrolipoyllysine-Residue Acetyltransferase - metabolism Female Granulosa Cells - drug effects Granulosa Cells - metabolism Mice Mice, Inbred C57BL Ovarian Follicle - drug effects Ovarian Follicle - growth & development Ovarian Follicle - metabolism Pyruvic Acid - metabolism
Increasing evidence has suggested that dihydrolipoamide S-acetyltransferase (DLAT), a subunit of the pyruvate dehydrogenase complex, is crucial for pyruvate metabolism and the regulation of cell death. The excessive death of granulosa cells (GCs) hinders the progression of follicular growth. However, the relationship between DLAT and follicular growth is poorly understood. Here, we found that pyruvate significantly shortened the age of pubertal initiation in mice and promoted follicular growth by promoting the proliferation of GCs. In addition, pyruvate up-regulated the expression of DLAT and the high level of DLAT was observed in large follicles, which were associated with follicular growth. Mechanistically, DLAT increased the mRNA and protein levels of proliferation pathways such as PCNA and MCL1 to promote GC proliferation. Additionally, DLAT bound to CASP3 and CASP9 proteins to inhibit the apoptosis of GCs. Taken together, these results reveal a mechanism that pyruvate regulated DLAT to promote follicular growth, and DLAT represents a promising target that supports new strategies for improving the growth of follicles.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.197 Molecular & Cell Biology - Mitochondria
1.197.2017 Lipoic Acid Metabolism
Web Of Science research areas
Cell Biology
ESI research areas
Biology & Biochemistry
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