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Updated: Jun 27, 2026

Cryopreservation and Bioenergetic Evaluation of Human Peripheral Blood Mononuclear Cells
Published on: October 20, 2023
Antioxidant therapy attenuates diabetes-related impairment of bone marrow stem cells
Mako Ohshima1, Tao-Sheng Li, Masayuki Kubo
1Department of Surgery and Clinical Science, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Background:
Bone marrow cells from humans and animals with diabetes exhibit decreased angiogenic potency, thought to be related to oxidative stress, so the present study investigated if antioxidant therapy would attenuate the diabetes-related impairment.
Methods And Results:
Diabetic mice were given antioxidant therapy, as a daily subcutaneous injection of superoxide dismutase-mimic (10 mg kg(-1) day(-1)). Diabetic and healthy mice given a vehicle treatment were used as the control. After 4 weeks of treatment, bone marrow mononuclear cells (BM-MNCs) were collected for analysis and the endothelial progenitor cells in BM-MNCs were evaluated by flow cytometry. The intracellular reactive oxygen species (ROS) levels in BM-MNCs were measured using 6-carboxy-2'7'-dichlorodihydrofluorescein diacetate. Endothelial differentiation from the BM-MNCs was estimated by immunostaining with VE-cadherin 7 days after culture. BM-MNCs from the control diabetic mice had fewer Flk-1/CD34 double-positive progenitor cells and higher intracellular ROS levels, with lower potency of endothelial differentiation than BM-MNCs from the healthy mice. Antioxidant therapy decreased the intracellular ROS level in BM-MNCs from that in the diabetic mice significantly (P<0.05), but increased significantly the percentage of endothelial progenitor cells (P<0.05) and their potency of differentiation into endothelial cells (P<0.05).
Conclusions:
Antioxidant therapy attenuated the diabetes-related impairment of BM-MNCs by reducing oxidative stress.
Insights
Antioxidant therapy improved bone marrow cell function in diabetic mice. This treatment reduced oxidative stress, enhancing endothelial progenitor cells and their differentiation potential, crucial for blood vessel formation.
Area of Science:
- * Regenerative Medicine
- * Oxidative Stress Research
- * Diabetes Complications
Background:
- * Diabetes mellitus is associated with impaired angiogenesis, potentially due to increased oxidative stress.
- * Bone marrow cells in diabetic individuals exhibit reduced angiogenic capacity.
- * This study explores antioxidant therapy as a potential intervention for diabetes-related vascular dysfunction.
Purpose of the Study:
- * To investigate whether antioxidant therapy can mitigate the diabetes-induced impairment of bone marrow mononuclear cells (BM-MNCs).
- * To assess the impact of antioxidant treatment on oxidative stress markers and endothelial progenitor cell function in diabetic mice.
Main Methods:
- * Diabetic and healthy mice were treated with a superoxide dismutase mimic or a vehicle control for four weeks.
- * Bone marrow mononuclear cells (BM-MNCs) were analyzed for endothelial progenitor cell populations (Flk-1/CD34) and intracellular reactive oxygen species (ROS) levels.
- * Endothelial differentiation potential of BM-MNCs was evaluated via VE-cadherin immunostaining.
Main Results:
- * Diabetic mice exhibited lower levels of endothelial progenitor cells and higher ROS levels in BM-MNCs compared to healthy controls.
- * Antioxidant therapy significantly reduced intracellular ROS levels in BM-MNCs from diabetic mice.
- * Treatment with antioxidant therapy significantly increased the percentage of endothelial progenitor cells and their differentiation capacity.
Conclusions:
- * Antioxidant therapy effectively attenuated diabetes-related impairments in bone marrow mononuclear cells.
- * The beneficial effects of antioxidant therapy are attributed to the reduction of oxidative stress.
- * This suggests a therapeutic strategy for improving angiogenic potential in diabetes.
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