ArticleReproductive sciences (Thousand Oaks, Calif.)2025
MyD88 Signaling in Sertoli Cells Mediates LPS-Induced Orchitis in Mice.
Article in Reproductive sciences (Thousand Oaks, Calif.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Advances in understanding the dual roles of testicular immune responses: From immune privilege to inflammation.Seminars in immunopathology · 2026Review
- Chronic stress drives oligoasthenozoospermia via gut microbiota-vitamin-Sting1/Slc9c2 axis.Nature communications · 2026Article
- Animal models of gut microbiota-male reproductive interactions: methodological assessment, translational bottlenecks, and optimization strategies.Frontiers in endocrinology · 2026Review
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Authors and funding
9 authors.
Funding
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Abstract
Orchitis, a prevalent male reproductive disorder that can severely impair fertility and potentially result in infertility. Sertoli cells orchestrate testicular immune responses during orchitis by modulating local inflammation and maintaining blood-testis barrier integrity. While Myeloid differentiation primary response protein 88 (MyD88), a critical adaptor molecule in the TLR4 signaling pathway, is known to mediate immune responses, its cell-specific role in Sertoli cells during lipopolysaccharide (LPS)-induced orchitis remains elusive. Using an murine orchitis model established through intraperitoneal LPS administration, we observed pronounced testicular inflammation concurrent with dramatic upregulation of MyD88 protein levels (P < 0.05). To further investigate the Sertoli cell-specific function of MyD88, we generated conditional Myd88 knockout (cKO) mice. Compared to controls, cKO mice showed marked attenuation of testicular edema along with improved sperm motility and viability post-LPS challenge. Myd88 deletion also suppressed LPS-triggered surges in pro-inflammatory cytokines (TNF-α, IL-6), maintained seminiferous tubule architecture, and mitigated neutrophil infiltration. Further studies demonstrated that Myd88 deletion rescued LPS-induced BTB disruption by restoring the expression of key BTB components (Connexin43, Claudin-11). Additionally, NF-κB signaling pathway is activated by MyD88 mediated inflammatory responses. Collectively, these findings uncover Sertoli cell specific MyD88 as a key regulator in LPS-induced orchitis pathogenesis, highlighting its potential as a promising therapeutic target for orchitis.
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Registered trials
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