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Comparative Analysis of the Therapeutic Effects of Amniotic Membrane and Umbilical Cord Derived Mesenchymal Stem Cells for the Treatment of Type 2 Diabetes.
Wang, Zhifeng; Li, Haisen; Fang, Jingmeng; Wang, Xiaoyu; Dai, Shuhang; Cao, Wei; Guo, Yinhong; Li, Zhe; Zhu, Hao.
  • Wang Z; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China. wangzhifeng68@hotmail.com.
  • Li H; Translational Medical Center for Stem Cell Therapy and Institute for Regenerative Medicine, Shanghai East Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092,
  • Fang J; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Wang X; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Dai S; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Cao W; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Guo Y; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Li Z; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
  • Zhu H; Sinoneural Cell Engineering Group Holdings Co., Ltd, Shanghai, 201100, China.
Stem Cell Rev Rep ; 18(3): 1193-1206, 2022 03.
Article in English | MEDLINE | ID: covidwho-1620352
ABSTRACT
Type 2 diabetes mellitus (T2DM), one of the most common carbohydrate metabolism disorders, is characterized by chronic hyperglycemia and insulin resistance (IR), and has become an urgent global health challenge. Mesenchymal stem cells (MSCs) originating from perinatal tissues such as umbilical cord (UC) and amniotic membrane (AM) serve as ideal candidates for the treatment of T2DM due to their great advantages in terms of abundant source, proliferation capacity, immunomodulation and plasticity for insulin-producing cell differentiation. However, the optimally perinatal MSC source to treat T2DM remains elusive. This study aims to compare the therapeutic efficacy of MSCs derived from AM and UC (AMMSCs and UCMSCs) of the same donor in the alleviation of T2DM symptoms and explore the underlying mechanisms. Our results showed that AMMSCs and UCMSCs displayed indistinguishable immunophenotype and multi-lineage differentiation potential, but UCMSCs had a much higher expansion capacity than AMMSCs. Moreover, we uncovered that single-dose intravenous injection of either AMMSCs or UCMSCs could comparably reduce hyperglycemia and improve IR in T2DM db/db mice. Mechanistic investigations revealed that either AMMSC or UCMSC infusion could greatly improve glycolipid metabolism in the liver of db/db mice, which was evidenced by decreased liver to body weight ratio, reduced lipid accumulation, upregulated glycogen synthesis, and increased Akt phosphorylation. Taken together, these data indicate that the same donor-derived AMMSCs and UCMSCs possessed comparable effects and shared a similar hepatoprotective mechanism on the alleviation of T2DM symptoms.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Mesenchymal Stem Cells / Hyperglycemia Type of study: Experimental Studies Topics: Vaccines Limits: Animals Language: English Journal: Stem Cell Rev Rep Year: 2022 Document Type: Article Affiliation country: S12015-021-10320-w

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Mesenchymal Stem Cells / Hyperglycemia Type of study: Experimental Studies Topics: Vaccines Limits: Animals Language: English Journal: Stem Cell Rev Rep Year: 2022 Document Type: Article Affiliation country: S12015-021-10320-w