AKAP12 maintains blood-testis barrier integrity and resists BPAF-induced male fertility impairment by inhibiting Src-mediated ZO-1 degradation
Most existing studies have focused on the direct reproductive toxicity of Bisphenol AF (BPAF), whereas the endogenous protective mechanisms within testicular tissues that defend against BPAF remain unclear. Blood-testis barrier (BTB), established by Sertoli cells, isolates the seminiferous tubule to provide an immune-privileged microenvironment that restricts toxins and supports spermatogenesis. As a scaffold protein orchestrating multiple signaling kinases, A-kinase anchor protein 12 (AKAP12) plays a critical role in various biological barriers. However, its functional relevance to the BTB has yet to be documented. Sertoli cell-specific Akap12 -deficient male mice were generated and exposed to BPAF via oral gavage for 28 days. Male reproductive function and sperm quality were evaluated by assessing fertility, sperm motility. BTB integrity was assessed using a biotin tracer assay and transmission electron microscopy (TEM). The effects of Src inhibition on ZO-1 phosphorylation and degradation were further evaluated in Akap12 -deficient Sertoli cells. We show that Sertoli cell-specific Akap12- deficient male mice exhibit markedly reduced fertility following BPAF exposure. Mechanistically, AKAP12 maintains BTB integrity by sequestering Src kinase. Lack of AKAP12 enhances Src (Tyr416) phosphorylation, which results in increased tyrosine phosphorylation of zonula occludens-1 (ZO-1), and ubiquitin-dependent degradation and subsequent destabilization of tight junction proteins, including Occludin and Claudin-11. Conversely, Src inhibitor administration effectively reverses AKAP12 deficiency-triggered ZO-1 phosphorylation and degradation in Sertoli cells. AKAP12 deficiency also disrupts extracellular matrix-integrin homeostasis. This study demonstrates that AKAP12 protects against BPAF-induced male fertility impairment by sequestering Src kinase, preserving tight junction integrity, and maintaining the BTB. Our findings extend AKAP12 research into reproductive toxicology and offer new insights into gene-environment interactions.
Authors
- Ying Xiong (ORCID: https://orcid.org/0000-0001-5109-1449)
- Zhengyu Hu (ORCID: https://orcid.org/0000-0001-6283-691X)
- Ji Hu (ORCID: https://orcid.org/0009-0005-5548-5994)
- Dan Cao (ORCID: https://orcid.org/0000-0002-9179-3311)
- Sanwei Guo (ORCID: https://orcid.org/0000-0001-6725-2841)
- Siyun Shen (ORCID: https://orcid.org/0009-0004-1635-1195)
- Shuowu Liu
- Chunyu Liu (ORCID: https://orcid.org/0000-0001-5357-3716)
- Lin Han (ORCID: https://orcid.org/0000-0001-9725-1946)
- Shiyu Mao (ORCID: https://orcid.org/0000-0003-4652-6828)
- Lili Xie (ORCID: https://orcid.org/0000-0002-8523-3158)
- Meiyu Bao
- Gaoxiang Gu
- Shuang Lu
- Lei Chen
- Shanhua Tang
- Shan Wang
- Feng Zhang
- Hongyang Wang
- Dongdong Xue
- Tao Li
Institutions
- Tongji University (CN)
- Ministry of Education of the People's Republic of China (CN)
- Second Military Medical University (CN)
- Shanghai Jiao Tong University (CN)
- Anhui Medical University (CN)
- Shanghai University of Traditional Chinese Medicine (CN)
- Longhua Hospital Shanghai University of Traditional Chinese Medicine (CN)
- International Peace Maternity & Child Health Hospital (CN)
- Hebei General Hospital (CN)
- Department of Embryology (US)
- Shanghai Tenth People's Hospital (CN)
- Shanghai First People's Hospital (CN)
- First Affiliated Hospital of Anhui Medical University (CN)
- Eastern Hepatobiliary Surgery Hospital (CN)
- Children's Hospital of Fudan University (CN)
Publication Details
- Journal
- Cellular and Molecular Life Sciences
- Published
- 2026-09-15
- DOI
- https://doi.org/10.1007/s00018-026-06424-6
- Primary Topic
- Barrier Structure and Function Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00