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Updated: Jan 14, 2026

Isolation of Sertoli Cells and Peritubular Cells from Rat Testes
Published on: February 8, 2016
A High-Fat Diet Damages the Blood-Testis Barrier Through the PCSK9-LOX1 Positive Feedback Loop in Sertoli Cells
Gao Zhang1, Zun Wang1, Man He1
1Department of Physiology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, 610041, China.
Abstract:
We primarily investigated the correlation between long-term high-fat diet and male infertility, aiming to reveal the potential mechanisms underlying PCSK9-induced spermatogenic dysfunction in this context. Clinical data revealed that infertile male patients typically exhibited hyperlipidemia and significantly elevated serum PCSK9 concentrations. To further explore this, we utilized wild-type C57BL/6 male mice and their homologous PCSK9-deficient mice, adhering to experimental control principles. After administering a high-fat diet to the experimental groups, we observed local testicular changes. Results indicated that the high-fat diet induced elevated PCSK9 levels in both the serum and testes while decreasing expression of ZO-1, a key protein in blood-testis barrier integrity. PCSK9 knockout effectively improved lipid metabolism in mice fed a high-fat diet and preserved blood-testis barrier integrity. Subsequently, we cultured Sertoli cells (TM4 cells) to explored underlying mechanisms under different treatments. Under high-lipid conditions, we discovered that LOX1-another lipid metabolism regulator was affected by PCSK9. PCSK9 increased LOX1 expression and, in turn, LOX1 increased PCSK9 expression. PCSK9 and LOX1 mutually promoted each other's expression, forming a positive feedback loop that reduced ZO-1 expression. Concurrently, both PCSK9 and LOX1 elevated OxLDL levels and increased TNF-α expression. In summary, the PCSK9-LOX1 feedback loop drives abnormally high OxLDL levels and cellular inflammation, ultimately downregulating the tight junction protein ZO-1 in blood-testis barrier, thereby potentially impairing testicular spermatogenesis.
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