MicroRNA-155 Promotes the Directional Migration of Resident Smooth Muscle Progenitor Cells by Regulating Monocyte Chemoattractant Protein 1 in Transplant Arteriosclerosis

Arterioscler Thromb Vasc Biol. 2016 Jun;36(6):1230-9. doi: 10.1161/ATVBAHA.115.306691. Epub 2016 Apr 14.

Abstract

Objective: Smooth muscle-like cells are major cell components of transplant arteriosclerosis lesions. This study investigated the origin of the smooth muscle-like cells, the mechanisms responsible for their accumulation in the neointima, and the factors that drive these processes.

Approach and results: A murine aortic transplantation model was established by transplanting miR-155(-/-) bone marrow cells into miR-155(+/+) mice. MicroRNA-155 was found to play a functional role in the transplant arteriosclerosis. Moreover, we found that the nonbone marrow-derived progenitor cells with markers of both early differentiated smooth muscles and stem cells in the allograft adventitia were smooth muscle progenitor cells. Purified smooth muscle progenitor cells expressed a mature smooth muscle cell marker when induced by platelet-derived growth factor-BB in vitro. In vivo, these cells could migrate into the intima from the adventitia and could contribute to the neointimal hyperplasia. The loss of microRNA-155 in bone marrow-derived cells decreased the concentration gradient of monocyte chemoattractant protein 1 between the intima and the adventitia of the allografts, which reduced the migration of smooth muscle progenitor cells from the adventitia into the neointima.

Conclusions: This study demonstrated that microRNA-155 promoted the directional migration of smooth muscle progenitor cells from the adventitia by regulating the monocyte chemoattractant protein 1 concentration gradient, which aggravated transplant arteriosclerosis.

Keywords: adventitia; arteriosclerosis; bone marrow; hyperplasia; stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adventitia / metabolism
  • Adventitia / pathology
  • Allografts
  • Animals
  • Aorta / metabolism
  • Aorta / pathology
  • Aorta / transplantation*
  • Atherosclerosis / etiology
  • Atherosclerosis / genetics
  • Atherosclerosis / metabolism*
  • Atherosclerosis / pathology
  • Bone Marrow Transplantation
  • Cell Differentiation
  • Cells, Cultured
  • Chemokine CCL2 / metabolism*
  • Chemotaxis*
  • Genotype
  • Hyperplasia
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Muscle, Smooth, Vascular / metabolism
  • Muscle, Smooth, Vascular / pathology
  • Muscle, Smooth, Vascular / transplantation*
  • Myocytes, Smooth Muscle / metabolism
  • Myocytes, Smooth Muscle / pathology
  • Myocytes, Smooth Muscle / transplantation*
  • Neointima
  • Phenotype
  • Signal Transduction
  • Stem Cells / metabolism*
  • Stem Cells / pathology
  • Time Factors
  • Transfection
  • Vascular Grafting / adverse effects*

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • MicroRNAs
  • Mirn155 microRNA, mouse