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Updated: Jan 21, 2026

In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
Dysregulation of lncRNA and circRNA Expression in Mouse Testes after Exposure to Triptolide
Suping Xiong1, Yanting Li1, Yang Xiang1
1Institute of Life Science and School of Life Science, Nanchang University, Nanchang, China.
Background:
Triptolide has been shown to exert various pharmacological effects on systemic autoimmune diseases and cancers. However, its severe toxicity, especially reproductive toxicity, prevents its widespread clinical use for people with fertility needs. Noncoding RNAs including lncRNAs and circRNAs are novel regulatory molecules that mediate a wide variety of physiological activities; they are crucial for spermatogenesis and their dysregulation might cause male infertility. However, whether they are involved in triptolide-induced reproductive toxicity is completely unknown.
Methods:
After exposure of mice to triptolide, the total RNAs were used to investigate lncRNA/circRNA/mRNA expression profiles by strand-specific RNA sequencing at the transcriptome level to help uncover RNA-related mechanisms in triptolide-induced toxicity.
Results:
Triptolide significantly decreased testicular weight, damaged testis and sperm morphology, and reduced sperm motility and density. Remarkable deformities in sperm head and tail were also found in triptolide-exposed mice. At the transcriptome level, the triptolide-treated mice exhibited aberrant expression profiles of lncRNAs/circRNAs/mRNAs. Gene Ontology and pathway analyses revealed that the functions of the differentially expressed lncRNA targets, circRNA cognate genes, and mRNAs were closely linked to many processes involved in spermatogenesis. In addition, some lncRNAs/circRNAs were greatly upregulated or inducibly expressed, implying their potential value as candidate markers for triptolide-induced male reproductive toxicity.
Conclusion:
This study provides a preliminary database of triptolide-induced transcriptome, promotes understanding of the reproductive toxicity of triptolide, and highlights the need for research on increasing the medical efficacy of triptolide and decreasing its toxicity.
Insights
Triptolide causes male reproductive toxicity by affecting sperm and altering noncoding RNA expression. This study reveals potential RNA markers for triptolide-induced male infertility.
Area of Science:
- Reproductive toxicology
- Transcriptomics
- Male infertility
Background:
- Triptolide shows therapeutic potential but has severe reproductive toxicity, limiting clinical use.
- Noncoding RNAs (lncRNAs, circRNAs) are vital for spermatogenesis; their dysregulation can cause male infertility.
- The role of noncoding RNAs in triptolide-induced reproductive toxicity is unknown.
Purpose of the Study:
- To investigate the molecular mechanisms of triptolide-induced male reproductive toxicity.
- To explore the involvement of noncoding RNAs (lncRNAs, circRNAs) in this toxicity.
- To identify potential RNA biomarkers for triptolide-induced male infertility.
Main Methods:
- Mice were exposed to triptolide.
- Strand-specific RNA sequencing was performed on total RNA to analyze lncRNA, circRNA, and mRNA expression profiles.
- Bioinformatic analyses (Gene Ontology, pathway analysis) were used to interpret the functional implications of altered gene expression.
Main Results:
- Triptolide exposure significantly reduced testicular weight, sperm count, and motility, and caused sperm morphology defects.
- Aberrant expression profiles of lncRNAs, circRNAs, and mRNAs were observed in triptolide-treated mice.
- Differentially expressed RNAs were functionally linked to spermatogenesis processes; some RNAs showed potential as toxicity markers.
Conclusions:
- This study provides a transcriptomic database for triptolide-induced toxicity.
- It enhances understanding of triptolide's adverse effects on male reproduction.
- Further research is needed to improve triptolide's therapeutic index by mitigating its toxicity.
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