TY - JOUR
T1 - The magnitude of exercise‐induced progenitor cell mobilisation and extravasation is positively associated with cardiorespiratory fitness
AU - Ross, Mark
AU - Aldred, Sarah
AU - Drayson, Mark T.
AU - Bosch, Jos A.
AU - Turner, James E.
PY - 2024/10/30
Y1 - 2024/10/30
N2 - CD34+ progenitor cells with angiogenic capabilities traffic into blood during exercise and extravasate afterwards but the magnitude of this response varies between people. We examined whether exercise-induced progenitor cell trafficking is influenced by cardiorespiratory fitness (maximum oxygen uptake; V̇O2max ). Ten males (age:23 ± 3 years; V̇O2max : 61.88 ± 4.68 mL kg min−1) undertook 1 h of treadmill running at 80% of V̇O2max. Blood samples were collected before exercise (Pre), in the final minute of exercise (0 h) and afterwards at 0.25, 1 and 24 h. Pan-progenitor cells(CD34+, CD34+CD45dim ) and putative endothelial progenitor cells (CD34+CD133+,CD34+VEGFR2+, CD34+CD45dimVEGFR2+) were quantified using flow cytometry. Progenitor subpopulations (except for CD34+CD45dimVEGFR2+) increased at 0 h(P < 0.05) and returned to pre-exercise levels by 1 h. V̇O2max was positively associated with the exercise-induced progenitor cell response and there were statistically significant time × V̇O2max interactions for CD34+, CD34+CD45dim and CD34+CD133+ subpopulations but not VEGFR2-expressing progenitor cells. There were statistically significant correlations between V̇O2max and ingress (r > 0.70, P < 0.025) and egress (r > −0.77, P < 0.009) of progenitor cell subsets (CD34+, CD34+CD45dim, CD34+CD133+), showing that cardiorespiratory fitness influences the magnitude of progenitor cell mobilisation into the blood and subsequent extravasation. These data may provide a link between high levels of cardiorespiratory fitness and vascular health.
AB - CD34+ progenitor cells with angiogenic capabilities traffic into blood during exercise and extravasate afterwards but the magnitude of this response varies between people. We examined whether exercise-induced progenitor cell trafficking is influenced by cardiorespiratory fitness (maximum oxygen uptake; V̇O2max ). Ten males (age:23 ± 3 years; V̇O2max : 61.88 ± 4.68 mL kg min−1) undertook 1 h of treadmill running at 80% of V̇O2max. Blood samples were collected before exercise (Pre), in the final minute of exercise (0 h) and afterwards at 0.25, 1 and 24 h. Pan-progenitor cells(CD34+, CD34+CD45dim ) and putative endothelial progenitor cells (CD34+CD133+,CD34+VEGFR2+, CD34+CD45dimVEGFR2+) were quantified using flow cytometry. Progenitor subpopulations (except for CD34+CD45dimVEGFR2+) increased at 0 h(P < 0.05) and returned to pre-exercise levels by 1 h. V̇O2max was positively associated with the exercise-induced progenitor cell response and there were statistically significant time × V̇O2max interactions for CD34+, CD34+CD45dim and CD34+CD133+ subpopulations but not VEGFR2-expressing progenitor cells. There were statistically significant correlations between V̇O2max and ingress (r > 0.70, P < 0.025) and egress (r > −0.77, P < 0.009) of progenitor cell subsets (CD34+, CD34+CD45dim, CD34+CD133+), showing that cardiorespiratory fitness influences the magnitude of progenitor cell mobilisation into the blood and subsequent extravasation. These data may provide a link between high levels of cardiorespiratory fitness and vascular health.
KW - cardiorespiratory fitness
KW - exercise
KW - progenitor cells
UR - https://www.scopus.com/pages/publications/85208064053
U2 - 10.1113/ep092041
DO - 10.1113/ep092041
M3 - Article
SN - 0958-0670
JO - Experimental Physiology
JF - Experimental Physiology
ER -