Arterial injury promotes medial chondrogenesis in Sm22 knockout mice

Cardiovasc Res. 2011 Apr 1;90(1):28-37. doi: 10.1093/cvr/cvq378. Epub 2010 Dec 22.

Abstract

Aims: Expression of SM22 (also known as SM22alpha and transgelin), a vascular smooth muscle cells (VSMCs) marker, is down-regulated in arterial diseases involving medial osteochondrogenesis. We investigated the effect of SM22 deficiency in a mouse artery injury model to determine the role of SM22 in arterial chondrogenesis.

Methods and results: Sm22 knockout (Sm22(-/-)) mice developed prominent medial chondrogenesis 2 weeks after carotid denudation as evidenced by the enhanced expression of chondrogenic markers including type II collagen, aggrecan, osteopontin, bone morphogenetic protein 2, and SRY-box containing gene 9 (SOX9). This was concomitant with suppression of VSMC key transcription factor myocardin and of VSMC markers such as SM α-actin and myosin heavy chain. The conversion tendency from myogenesis to chondrogenesis was also observed in primary Sm22(-/-) VSMCs and in a VSMC line after Sm22 knockdown: SM22 deficiency altered VSMC morphology with compromised stress fibre formation and increased actin dynamics. Meanwhile, the expression level of Sox9 mRNA was up-regulated while the mRNA levels of myocardin and VSMC markers were down-regulated, indicating a pro-chondrogenic transcriptional switch in SM22-deficient VSMCs. Furthermore, the increased expression of SOX9 was mediated by enhanced reactive oxygen species production and nuclear factor-κB pathway activation.

Conclusion: These findings suggest that disruption of SM22 alters the actin cytoskeleton and promotes chondrogenic conversion of VSMCs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carotid Artery Injuries / genetics
  • Carotid Artery Injuries / metabolism
  • Carotid Artery Injuries / pathology*
  • Cell Transdifferentiation* / genetics
  • Cells, Cultured
  • Chondrocytes / metabolism
  • Chondrocytes / pathology*
  • Chondrogenesis* / genetics
  • Disease Models, Animal
  • Gene Expression Regulation
  • Genotype
  • Male
  • Metaplasia
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microfilament Proteins / deficiency*
  • Microfilament Proteins / genetics
  • Muscle Development
  • Muscle Proteins / deficiency*
  • Muscle Proteins / genetics
  • Muscle, Smooth, Vascular / injuries
  • Muscle, Smooth, Vascular / metabolism
  • Muscle, Smooth, Vascular / pathology*
  • Myocytes, Smooth Muscle / metabolism
  • Myocytes, Smooth Muscle / pathology*
  • NF-kappa B / metabolism
  • Oxidation-Reduction
  • Phenotype
  • RNA Interference
  • RNA, Messenger / metabolism
  • Rats
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Transfection
  • Tunica Media / injuries
  • Tunica Media / metabolism
  • Tunica Media / pathology*
  • Vascular System Injuries / genetics
  • Vascular System Injuries / metabolism
  • Vascular System Injuries / pathology*

Substances

  • Microfilament Proteins
  • Muscle Proteins
  • NF-kappa B
  • RNA, Messenger
  • Reactive Oxygen Species
  • Tagln protein, mouse
  • Transcription Factors