PT  - JOURNAL ARTICLE
AU  - Mengxi Sun
AU  - Andrew M Cobb
AU  - Robert Hayward
AU  - Qiuping P Zhang
AU  - Melinda Duer
AU  - Rukshana Shroff
AU  - Catherine M Shanahan
TI  - 225 The role of the dna damage response in vascular calcification
AID  - 10.1136/heartjnl-2017-311726.223
DP  - 2017 Jun 01
TA  - Heart
PG  - A145--A146
VI  - 103
IP  - Suppl 5
4099  - http://heart.bmj.com/content/103/Suppl_5/A145.2.short
4100  - http://heart.bmj.com/content/103/Suppl_5/A145.2.full
SO  - Heart2017 Jun 01; 103
AB  - Introduction Vascular calcification is a hallmark of vascular ageing, and associated with vascular smooth muscle cell (VSMC) death, phenotype modulation and maladaptation. However, it remains unclear how the initial stress signals link to these downstream cellular events. Emerging evidence and our in vitro data suggest that stress may drive vascular calcification through elevated levels of DNA damage, a key factor driving cellular ageing.Methods and Results We investigated the effects of different DNA damage signalling pathway inhibitors (ATM, ATM/ATR and PARP1) on the progression of vascular calcification. Using comet assays and western blot, we found elevated levels of DNA damage in calcified VSMCs and that inducing DNA damage accelerated rates of calcification. Chemical inhibition or siRNA knockdown of ATM, ATM/ATR or PARP signalling reduced or delayed calcification and prevented cells undergoing calcification-associated phenotype changes including osteo/chondrogenic differentiation. Prevention was associated with down-regulation of senescence and inflammatory markers suggesting the senescence associated secretory phenotype (SASP) acts to potentiate VSMC calcification.Conclusion Taken together, these in vitro data suggest DNA damage signalling is involved in the pathological regulation of calcification. Therefore, interventions that reduce DNA damage, promote DNA damage repair, or modulate DNA damage signalling could be potential therapies for the prevention of vascular calcification.