期刊
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
卷 322, 期 4, 页码 H537-H548出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00612.2021
关键词
heart failure; inflammation; myocardial infarction; remodeling
资金
- National Institutes of Health [U54GM115458, HL137319]
- Biomedical Laboratory Research and Development Service of the Veterans Affairs Office of Research and Development Grant [5I01BX000505]
- Swedish Society for Medical Research Grant [P19-0144]
The speed of skin wound healing predicts the healing response of the heart after myocardial infarction. Two plasma proteins, EAF1 and A2M, at day 3 of myocardial infarction can predict the risk of death in 66% of cases. ApoD negatively regulates skin and cardiac wound healing by promoting inflammation. Skin acts as a reflection of the heart, with common pathways linking wound healing across different organs.
Both skin wound healing and the cardiac response to myocardial infarction (MI) progress through similar pathways involving inflammation, resolution, tissue repair, and scar formation. Due to the similarities, we hypothesized that the healing response to skin wounding would predict future response to MI. Mice were given a 3-mm skin wound using a disposable biopsy punch and the skin wound was imaged daily until closure. The same set of animals was given MI by permanent coronary artery ligation 28 days later and followed for 7 days. Cardiac physiology was measured by echocardiography at baseline and MI days 3 and 7. Animals that survived until day 7 were grouped as survivors, and animals that died from MI were grouped as nonsurvivors. Survivors had faster skin wound healing than nonsurvivors. Faster skin wound healing predicted MI survival better than commonly used cardiac functional variables (e.g., infarct size, fractional shortening, and end diastolic dimension). N-glycoproteome profiling of MI day 3 plasma revealed alpha(2)-macroglobufin and ELL-associated factor 1 as strong predictors of future MI death and progression to heart failure. A second cohort of MI mice validated these findings. To investigate the clinical relevance of alpha(2)-macroglobulin, we mapped the plasma glycoproteome in patients with MI 48 h after admission and in healthy controls. In patients, alpha(2)-macroglobulin was increased 48 h after MI. Apolipoprotein D, another plasma glycoprotein, detrimentally regulated both skin and cardiac wound healing in male but not female mice by promoting inflammation. Our results reveal that the skin is a mirror to the heart and common pathways link wound healing across organs. NEW & NOTEWORTHY Faster skin wound healers had more efficient cardiac healing after myocardial infarction (MI). Two plasma proteins at D3 MI, EAF1 and A2M, predicted MI death in 66% of cases. ApoD regulated both skin and cardiac wound healing in male mice by promoting inflammation. The skin was a mirror to the heart and common pathways linked wound healing across organs.
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