Ginsenoside Rg1 as an Effective Regulator of Mesenchymal Stem Cells

被引:33
|
作者
He, Fang [1 ,2 ]
Yu, Changyin [3 ]
Liu, Tao [3 ]
Jia, Huilin [4 ]
机构
[1] Zunyi Med Univ, Key Lab Cell Engn Guizhou Prov, Affiliated Hosp, Zunyi, Peoples R China
[2] Univ Hosp Tubingen, Dept Oral & Maxillofacial Surg, Tubingen, Germany
[3] Zunyi Med Univ, Affiliated Hosp, Dept Neurol, Zunyi, Guizhou, Peoples R China
[4] Xian Med Univ, Sch Stomatol, Xian, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2020年 / 10卷
关键词
ginsenoside Rg1; mesenchymal stem cells; proliferation; differentiation; apoptosis; senescence; preclinical study; TERT-BUTYL HYDROPEROXIDE; UMBILICAL-CORD BLOOD; BONE-MARROW; PANAX-GINSENG; INDUCED APOPTOSIS; PHENOTYPE DIFFERENTIATION; BALLOON ANGIOPLASTY; GENE-EXPRESSION; STROMAL CELLS; MECHANISMS;
D O I
10.3389/fphar.2019.01565
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recently, breakthroughs have been made in the use of mesenchymal stem cells (MSCs) to treat various diseases. Several stem cell types have been authorized as drugs by the European Medicines Agency and the U.S. Food and Drug Administration. The Chinese official document "Notification of the management of stem cell clinical research (trial)" was also published in August 2015. Currently, China has approved 106 official stem cell clinical research filing agencies and 62 clinical research projects, which are mostly focused on MSC therapy. Hence, the optimization and development of stem cell drugs is imperative. During this process, maximizing MSC expansion, minimizing cell loss during MSC transplantation, improving the homing rate, precisely regulating the differentiation of MSCs, and reducing MSC senescence and apoptosis are major issues in MSC preclinical research. Similar to artemisinin extracted from the stems and leaves of Artemisia annua, ginsenoside Rg1 (Rg1) is purified from the root or stem of ginseng. In the human body, Rg1 regulates organ function, which is inseparable from its regulation of adult stem cells. Rg1 treatment may effectively regulate the proliferation, differentiation, senescence, and apoptosis of MSCs in different microenvironments in vitro or in vivo. In this review, we discuss recent advances in understanding the effect of Rg1 on MSCs and describe the issues that must be addressed and prospects regarding Rg1 regulation of MSCs in preclinical or clinical studies.
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页数:12
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