Affiliation:
1. Department of Cardiology Nagoya University Graduate School of Medicine Nagoya Japan
2. Division of Cardiothoracic Surgery Department of Surgery Carlyle Fraser Heart Center Emory University School of Medicine Atlanta GA
3. Department of Advanced Cardiovascular Therapeutics Nagoya University Graduate School of Medicine Nagoya Japan
Abstract
Background
Circadian rhythm disorders, often seen in modern lifestyles, are a major social health concern. The aim of this study was to examine whether circadian rhythm disorders would influence angiogenesis and blood perfusion recovery in a mouse model of hind limb ischemia.
Methods and Results
A jet‐lag model was established in C57BL/6J mice using a light‐controlled isolation box. Control mice were kept at a light/dark 12:12 (12‐hour light and 12‐hour dark) condition. Concentrations of plasma vascular endothelial growth factor and circulating endothelial progenitor cells in control mice formed a circadian rhythm, which was diminished in the jet‐lag model (
P
<0.05). The jet‐lag condition deteriorated tissue capillary formation (
P
<0.001) and tissue blood perfusion recovery (
P
<0.01) in hind limb ischemia, which was associated with downregulation of vascular endothelial growth factor expression in local ischemic tissue and in the plasma. Although the expression of clock genes (ie,
Clock
,
Bmal1
, and
Cry
) in local tissues was upregulated after ischemic injury, the expression levels of cryptochrome (Cry) 1 and Cry2 were inhibited by the jet‐lag condition. Next,
Cry1
and
Cry2
double‐knockout mice were examined for blood perfusion recoveries and a reparative angiogenesis.
Cry1
and
Cry2
double‐knockout mice revealed suppressed capillary density (
P
<0.001) and suppressed tissue blood perfusion recovery (
P
<0.05) in the hind limb ischemia model. Moreover, knockdown of
CRY1/2
in human umbilical vein endothelial cells was accompanied by increased expression of
WEE1
and decreased expression of
HOXC5
. This was associated with decreased proliferative capacity, migration ability, and tube formation ability of human umbilical vein endothelial cells, respectively, leading to impairment of angiogenesis.
Conclusions
Our data suggest that circadian rhythm disorder deteriorates reparative ischemia‐induced angiogenesis and that maintenance of circadian rhythm plays an important role in angiogenesis.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Cited by
14 articles.
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