Vigorous exercise mobilizes CD34+hematopoietic stem cells to peripheral blood via the β2-adrenergic receptor

被引:41
作者
Agha, Nadia H. [1 ]
Baker, Forrest L. [1 ]
Kunz, Hawley E. [1 ]
Graff, Rachel [1 ]
Azadan, Rod [1 ]
Dolan, Chad [1 ]
Laughlin, Mitzi S. [1 ]
Hosing, Chitra [2 ]
Markofski, Melissa M. [1 ]
Bond, Richard A. [3 ]
Bollard, Catherine M. [4 ,5 ]
Simpson, Richard J. [1 ,6 ,7 ,8 ]
机构
[1] Univ Houston, Dept Hlth & Human Performance, Lab Integrated Physiol, 3875 Holman St, Houston, TX 77204 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[3] Univ Houston, Dept Pharmacol & Pharmaceut Sci, Houston, TX USA
[4] Childrens Natl Hlth Syst, Program Cell Enhancement & Technol Immunotherapy, Washington, DC USA
[5] George Washington Univ, Washington, DC USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Behav Sci, Houston, TX 77030 USA
[7] Univ Arizona, Dept Nutr Sci, 1177 E Fourth St,Shantz Bldg,Room 308, Tucson, AZ 85721 USA
[8] Univ Arizona, Dept Pediat, 1177 E Fourth St,Shantz Bldg,Room 308, Tucson, AZ 85721 USA
关键词
Hematopoietic stem cell transplantation; Exercise immunology; Exercise intensity; CD133; beta-AR blockade; Progenitor cells; Nadolol; Bisoprolol; Granulocyte colony stimulating factor (G-CSF); ENDOTHELIAL PROGENITOR CELLS; COLONY-STIMULATING FACTOR; HEMATOPOIETIC STEM; SKELETAL-MUSCLE; BONE-MARROW; PHARMACOKINETICS; PLERIXAFOR; NADOLOL; SELECTIVITY; BISOPROLOL;
D O I
10.1016/j.bbi.2017.10.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute dynamic exercise mobilizes CD34+ hematopoietic stem cells (HSCs) to the bloodstream, potentially serving as an economical adjuvant to boost the collection of HSCs from stem cell transplant donors. The mechanisms responsible for HSC mobilization with exercise are unknown but are likely due to hemodynamic perturbations, endogenous granulocyte-colony stimulating factor (G-CSF), and/or beta(2)-adrenergic receptor (beta(2)-AR) signaling. We characterized the temporal response of HSC mobilization and plasma G-CSF following exercise, and determined the impact of in vivo beta-AR blockade on the exercise-induced mobilization of HSCs. Healthy runners (n = 15) completed, in balanced order, two single bouts of steady state treadmill running exercise at moderate (lasting 90-min) or vigorous (lasting 30-min) intensity. A separate cohort of healthy cyclists (n = 12) completed three 30-min cycling ergometer trials at vigorous intensity after ingesting: (i) 10 mg bisoprolol (beta(1)-AR antagonist); (ii) 80 mg nadolol (beta(1) + beta(2)-AR antagonist); or (iii) placebo, in balanced order with a double-blind design. Blood samples collected before, during (runners only), immediately after, and at several points during exercise recovery were used to determine circulating G-CSF levels (runners only) and enumerate CD34+ HSCs by flow cytometry (runners and cyclists). Steady state vigorous but not moderate intensity exercise mobilized HSCs, increasing the total blood CD34+ count by similar to 4.15 +/- 1.62 Delta cells/mu l (+202 +/- 92%) compared to resting conditions. Plasma G-CSF increased in response to moderate but not vigorous exercise. Relative to placebo, nadolol and bisoprolol lowered exercising heart rate and blood pressure to comparable levels. The number of CD34+ HSCs increased with exercise after the placebo and bisoprolol trials, but not the nadolol trial, suggesting beta(2)-AR signaling mediated the mobilization of CD34+ cells [Placebo: 2.10 +/- 1.16 (207 +/- 69.2%), Bisoprolol 1.66 +/- 0.79 (+163 +/- 29%), Nadolol: 0.68 +/- 0.54 (+143 +/- 36%) Delta cells/mu L]. We conclude that the mobilization of CD34+ HSCs with exercise is not dependent on circulating G-CSF and is likely due to the combined actions of beta(2)-AR signaling and hemodynamic shear stress. (C) 2017 Published by Elsevier Inc.
引用
收藏
页码:66 / 75
页数:10
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