Abstract

Age-related regression in hematopoietic stem/progenitor cells (HSC/HPCs) limits replenishment of the blood and immune system and hence contributes to hematopoietic diseases and declined immunity. In this study, we employed D-gal-induced aging mouse model and observed the antiaging effects of Angelica Sinensis Polysaccharide (ASP), a major active ingredient in dong quai (Chinese Angelica Sinensis), on the Sca-1+ HSC/HPCs in vivo. ASP treatment prevents HSC/HPCs senescence with decreased AGEs levels in the serum, reduced SA-β-Gal positive cells, and promoted CFU-Mix formation in the D-gal administrated mouse. We further found that multiple mechanisms were involved: (1) ASP treatment prevented oxidative damage as total antioxidant capacity was increased and levels of reactive oxygen species (ROS), 8-OHdG, and 4-HNE were declined, (2) ASP reduced the expression of γ-H2A.X which is a DNA double strand breaks (DSBs) marker and decreased the subsequent ectopic expressions of effectors in p16Ink4a-RB and p19Arf-p21Cip1/Waf senescent pathways, and (3) ASP inhibited the excessive activation of Wnt/β-catenin signaling in aged HSC/HPCs, as the expressions of β-catenin, phospho-GSK-3β, and TCF-4 were decreased, and the cyto-nuclear translocation of β-catenin was inhibited. Moreover, compared with the positive control of Vitamin E, ASP exhibited a better antiaging effect and a weaker antioxidation ability, suggesting a novel protective role of ASP in the hematopoietic system.

Highlights

  • Hematopoietic pathophysiological changes like chronic anemia, decreased adaptive immune competence, and increased incidence of leukemia are closely associated with age [1]

  • The accumulation of advanced glycation end products (AGEs) in serum and tissues is an important biological indicator to evaluate the aging of the body [15]

  • By evaluating reactive oxygen species (ROS) levels and contents of 4-HNE, 8-OHdG, and total antioxidant capacity (T-AOC) in the Sca-1+ HSC/HPCs we explored whether the antiaging effect of Angelica Sinensis Polysaccharide (ASP) was mediated by alleviating oxidative stress

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Summary

Introduction

Hematopoietic pathophysiological changes like chronic anemia, decreased adaptive immune competence, and increased incidence of leukemia are closely associated with age [1]. HSC/HPCs with self-renewal and multilineage potential are the ancestor of all blood cells and lymphocytes. Exploring the possibility and the underlying mechanisms to delay HSC/HPCs senescence may provide promising ways to treat the age-related hematopoietic diseases and improve the quality of the senior life. Our recent studies have indicated an extraordinary antiaging role of ASP which protected HSC/HPCs against X-ray-irradiation-induced aging by inhibiting oxidative stress damage [4], alleviating DNA damage, and increasing telomerase activity [5]. It still requires investigation in a more physiological-like aging model and further exploration of the molecular mechanisms

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