Modulation of miR29a improves impaired post-ischemic angiogenesis in hyperglycemia

被引:29
作者
Chen, Lingdan [1 ,2 ]
Okeke, Emmanuel [3 ]
Ayalew, Dawit [1 ,2 ]
Wang, Danny [1 ,2 ]
Shahid, Lyeba [1 ,2 ]
Dokun, Ayotunde O. [3 ]
机构
[1] Univ Virginia, Sch Med, Dept Med, Div Endocrinol, Charlottesville, VA 22910 USA
[2] Univ Virginia, Sch Med, Robert M Berne Cardiovasc Res Ctr, Charlottesville, VA 22910 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Med, Div Endocrinol Diabet & Metab, Memphis, TN 38163 USA
关键词
MicroRNA; miR29; peripheral arterial disease; hyperglycemia; angiogenesis; PERIPHERAL ARTERIAL-DISEASE; NITRIC-OXIDE SYNTHASE; PERFUSION RECOVERY; DIABETES-MELLITUS; ENDOTHELIAL-CELLS; HINDLIMB ISCHEMIA; VASCULAR-DISEASE; EXPRESSION; MICRORNA-16; DYSFUNCTION;
D O I
10.1177/1535370217716424
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Individuals with diabetes mellitus suffer from impaired angiogenesis and this contributes to poorer peripheral arterial disease outcomes. In experimental peripheral arterial disease, angiogenesis and perfusion recovery are impaired in mice with diabetes. We recently showed that a disintegrin and metalloproteinase domain-containing protein 12 (ADAM12) is upregulated in ischemic endothelial cells and plays a key role in post-ischemic angiogenesis and perfusion recovery following experimental peripheral arterial disease. Here we investigated the role of miR29a in the regulation of endothelial cell ADAM12 expression in ischemia and how hyperglycemia negatively affects this regulation. We also explored whether modulating miR29a can improve impaired post-ischemic angiogenesis associated with hyperglycemia. Additionally, we tested whether miR29a modulation could improve post ischemic angiogenesis in the setting of impaired vascular endothelial growth factor signaling. We forced miR29a expression in ischemic endothelial cells and assessed ADAM12 expression. We also evaluated whether hyperglycemia invivo and invitro impair ischemia-induced ADAM12 upregulation and miR29a downregulation. Lastly, we determined whether modulating endothelial cell miR29a expression in ischemia and hyperglycemia could improve impaired endothelial cell functions. We found under ischemic conditions where ADAM12 is upregulated in endothelial cells, miR29a is downregulated. Forced expression of miR29a in ischemic endothelial cell prevented ADAM12 upregulation. In ischemic hind limbs of mice with type 1 diabetes and in endothelial cells exposed to simulated ischemia plus hyperglycemia, ADAM12 upregulation and miR29a downregulation were blunted while angiogenesis was impaired. Knocking down miR29a with an miR29a inhibitor was sufficient to improve ADAM12 upregulation and angiogenesis in simulated ischemia plus hyperglycemia. It was also sufficient to improve perfusion recovery in type 1 diabetes mellitus mice invivo and angiogenesis invitro even when vascular endothelial growth factor signaling was impaired with blocking antibodies. In conclusion, MiR29a regulates endothelial cell ADAM12 upregulation in ischemia and this is impaired in hyperglycemia. Modulating miR29a improves impaired post-ischemic angiogenesis associated with hyperglycemia.
引用
收藏
页码:1432 / 1443
页数:12
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