Acta Veterinaria et Zootechnica Sinica ›› 2025, Vol. 56 ›› Issue (11): 5563-5574.doi: 10.11843/j.issn.0366-6964.2025.11.017

• Animal Biotechnology and Reproduction • Previous Articles     Next Articles

Effects of L-Malic Acid on the Proliferation and Transcriptional Profile of Porcine Ovarian Granulosa Cells

ZHAO Xiaoyi1,2(), ZHU Longlong3, LIU Hui2, ZHANG Dongyan2, CAI Long2, WANG Yalei2, WANG Jing2, ZHAO Junxing1,*(), CHEN Meixia2,*()   

  1. 1. College of Animal Science, Shanxi Agricultural University, Taigu 030801, China
    2. Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China
    3. College of Animal Science and Technology, Henan University of Science and Technology, Luoyang 471023, China
  • Received:2025-04-18 Online:2025-11-23 Published:2025-11-27
  • Contact: ZHAO Junxing, CHEN Meixia E-mail:zxy_9z@163.com;junxzh@163.com;meixia10nian@163.com

Abstract:

The present study was designed to examine the effects of L-malic acid (L-MA) on the cell proliferation of porcine ovarian granulosa cells (PGCs) and to uncover the potential mechanism based on transcriptomic analysis. In this study, primary PGCs were isolated, cultured and randomly assigned to either a control group or L-MA treatment groups (10, 25, 50, 100, and 200 μmol·L-1). CCK-8 assay, EdU incorporation assay (5-ethynyl-2'-deoxyuridine) and qPCR analysis were used to assess the cell viability and cell proliferation. Furthermore, RNA sequencing (RNA-seq) was employed to delineate L-MA-induced the transcriptional landscape alterations in PGCs. Compared with the control group, 25, 50, 100 and 200 μmol·L-1 L-MA significantly increased cell viability of PGCs (P < 0.05). PGCs exhibited the highest cell viability at an L-MA final concentration of 50 μmol·L-1. Treatment with 50 μmol·L-1 L-MA markedly upregulated the mRNA expression of proliferating cell nuclear antigen (PCNA) (P < 0.01), a key proliferation marker, and enhanced the proportion of EdU-positive cells in PGCs. Transcriptomic analysis revealed that under the threshold of |FC|≥1.5 and P < 0.05, 169 significantly upregulated and 118 downregulated genes were identified in PGCs with L-MA exposure. GO enrichment analysis demonstrated that differentially expressed genes (DEGs) were predominantly enriched in cellular components related to cell cycle complexes and nucleases, with molecular functions and biological processes related to genetic material replication, epigenetic modification, substance transport and metabolism, as well as cell proliferation and differentiation. KEGG and GSEA analyses further indicated that DEGs were primarily involved in signaling pathways associated with cellular immunity, genetic material replication, substance metabolism, and reproductive functions. Notably, predictions of transcription factor (TF) and binding sequences between TF and TF's target genes suggested that ELF3 was identified as the most likely candidate transcriptional factor mediated by L-MA, with potential binding sites within the PCNA promoter region. In summary, the findings demonstrate that L-MA significantly enhances the proliferation of porcine ovarian granulosa cells. This proliferative effect may be attributed to L-MA-mediated regulation of gene expression involving cell cycle complexes and nucleases, enhancement of molecular functions and biological processes related to genetic material replication, epigenetic modification, and substance transport, as well as improvement of cell health. This study provides important scientific evidence for the potential application of L-malic acid-based products in modulating granulosa cell proliferation and ovarian function.

Key words: L-malic acid, porcine ovarian granulosa cells, cell proliferation, transcriptome analysis

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