Article ID Journal Published Year Pages File Type
1906738 Experimental Gerontology 2010 6 Pages PDF
Abstract

The accumulation of senescent cells within tissues can potentially lead to biological dysfunction and manifestation of disease associated with ageing. The majority of senescent cells display a commonly altered secretome similar to a wound healing response (termed the senescence-associated secretory phenotype or SASP), which could have deleterious implications on the tissue microenvironment. However, senescent cells also appear to have a cell-type (or even cell-strain) exclusive senescent phenotype (CESP), an area of research that is underexplored. One such CESP is the pro-calcificatory phenotype recently reported in senescent vascular smooth muscle cells (VSMCs). Senescent VSMCs have been shown to overexpress genes and proteins (including RUNX-2, alkaline phosphatase (ALP), type I collagen and BMP-2) associated with osteoblasts, leading to partial osteoblastic transdifferentiation. As such, it has been suggested that senescent VSMCs contribute to cardiovascular dysfunction through induction of vascular calcification. This review discusses recent findings on VSMC senescence and their potential role in the pathophysiology of vascular calcification.

Research Highlights►(1) Senescent vascular smooth muscle cells adopt an osteoblastic phenotype. ►(2) Role of VSMC senescence in the pathophysiology of vascular calcification. ►(3) Cell-type exclusive senescent phenotype (CESP) in ageing and disease development.

Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
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