Tho complex-dependent posttranscriptional control contributes to vascular smooth muscle cell fate decision

Xinli Yuan, Tao Zhang, Fang Yao, Yingnan Liao, Fei Liu, Zongna Ren, Leng Han, Lixia Diao, Yankui Li, Bingying Zhou, Fan He, Li Wang

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Rationale: Modulation of vascular smooth muscle cell (VSMC) phenotype plays a fundamental role in vascular development and diseases. Although extensive studies uncovered the roles of transcriptional regulation in VSMCspecific gene expression, how posttranscriptional regulation contributes to VSMC fate decisions remains to be determined. Objective: To establish THO complex-dependent VSMC gene expression as a novel regulatory basis controlling VSMC phenotypes. Methods and Results: Immunohistochemical staining against THOC2 and THOC5, 2 components of the THO complex, revealed a dramatic reduction in their expression in human arteries undergoing carotid endarterectomy compared with normal internal mammary arteries. Silencing of THOC2 or THOC5 led to dedifferentiation of VSMCs in vitro, characterized by decreased VSMC marker gene expression and increased migration and proliferation. Furthermore, RNA high-throughput sequencing (Seq) revealed that THOC5 silencing closely resembled the gene expression changes induced on PDGF (platelet-derived growth factor)-BB/PDGF-DD treatments in cultured VSMCs. Mechanistically, THOC2 and THOC5 physically interacted with and functionally relied on each other to bind to specific motifs on VSMC marker gene mRNAs. Interestingly, mRNAs that lost THOC2 or THOC5 binding during VSMC dedifferentiation were enriched for genes important for the differentiated VSMC phenotype. Last, THOC5 overexpression in injured rat carotid arteries significantly repressed loss of VSMC marker gene expression and neointima formation. Conclusions: Our data introduce dynamic binding of THO to VSMC marker gene mRNAs as a novel mechanism contributing to VSMC phenotypic switching and imply THOC5 as a potential intervention node for vascular diseases.

Original languageEnglish
Pages (from-to)538-549
Number of pages12
JournalCirculation Research
Issue number5
StatePublished - 2018
Externally publishedYes


  • Carotid arteries
  • Endarterectomy
  • Gene expression
  • Neointima
  • Vascular diseases


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