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Lower resting and exercise-induced circulating angiogenic progenitors and angiogenic T cells in older men
Mark D Ross1, Eva M Malone1, Richard Simpson2,3
1School of Applied Sciences, Edinburgh Napier University , Edinburgh , United Kingdom.
Insights
Older adults have fewer circulating angiogenic cells (CACs) and impaired exercise-induced responses, potentially increasing cardiovascular disease risk. Cardiorespiratory fitness did not influence these age-related changes in CACs.
Area of Science:
- Cardiovascular Science
- Aging Research
- Cellular Biology
Background:
- Aging is linked to endothelial dysfunction and reduced vascular repair capacity.
- Circulating angiogenic cells (CACs) are crucial for maintaining cardiovascular health and decline with age.
- The interplay between cardiorespiratory fitness (CRF), aging, and CAC function remains unclear.
Purpose of the Study:
- To investigate the relationship between age, cardiorespiratory fitness (CRF), and the frequency of circulating angiogenic cells (CACs) in healthy men.
- To determine the exercise-induced responsiveness of CACs in older versus younger individuals.
Main Methods:
- Study 1: 107 healthy men (18-75 yr) underwent CRF assessment and blood sampling for CAC enumeration (EPCs, TANG, CXCR4+ cells).
- Study 2: 17 healthy men (young vs. older) performed a 30-min cycling bout, with CACs measured pre- and post-exercise.
- Flow cytometry was used to quantify specific CAC subsets and their receptor expression.
Main Results:
- Age was inversely associated with CD34+ progenitor cells, TANG cells, and CXCR4-expressing CACs.
- CRF was not independently associated with CAC subsets after adjusting for age.
- Older men exhibited significantly lower resting CAC levels and attenuated exercise-induced increases in CACs compared to younger men.
Conclusions:
- Older adults possess lower levels of circulating angiogenic cells, irrespective of CRF.
- Reduced CACs in older individuals may contribute to heightened cardiovascular disease risk.
- Impaired exercise-induced mobilization of CACs in older adults suggests diminished vascular repair capacity with aging.
Abstract:
Aging is associated with a dysfunctional endothelial phenotype as well as reduced angiogenic capabilities. Exercise exerts beneficial effects on the cardiovascular system, possibly by increasing/maintaining the number and/or function of circulating angiogenic cells (CACs), which are known to decline with age. However, the relationship between cardiorespiratory fitness (CRF) and age-related changes in the frequency of CACs, as well as the exercise-induced responsiveness of CACs in older individuals, has not yet been determined. One-hundred seven healthy male volunteers, aged 18-75 yr, participated in study 1. CRF was estimated using a submaximal cycling ergometer test. Circulating endothelial progenitor cells (EPCs), angiogenic T cells (TANG), and their chemokine (C-X-C motif) receptor 4 (CXCR4) cell surface receptor expression were enumerated by flow cytometry using peripheral blood samples obtained under resting conditions before the exercise test. In study 2, 17 healthy men (8 young men, 18-25 yr; 9 older men, 60-75 yr) were recruited, and these participants undertook a 30-min cycling exercise bout at 70% maximal O2 consumption, with CACs enumerated before and immediately after exercise. Age was inversely associated with both CD34+ progenitor cells ( r2 = -0.140, P = 0.000) and TANG ( r2 = -0.176, P = 0.000) cells as well as CXCR4-expressing CACs (CD34+: r2 = -0.167, P = 0.000; EPCs: r2 = -0.098, P = 0.001; TANG: r2 = -0.053, P = 0.015). However, after correcting for age, CRF had no relationship with either CAC subset. In addition, older individuals displayed attenuated exercise-induced increases in CD34+ progenitor cells, TANG, CD4+, TANG, and CD8+CXCR4+ TANG cells. Older men display lower CAC levels, which may contribute to increased risk of cardiovascular disease, and older adults display an impaired exercise-induced responsiveness of these cells. NEW & NOTEWORTHY Older adults display lower circulating progenitor cell and angiogenic T cell counts compared with younger individuals independently of cardiometabolic risk factors and cardiorespiratory fitness. Older adults also display impaired exercise-induced mobilization of these vasculogenic cells.
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