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CD34- human placenta-derived mesenchymal stem cells protect against heat stroke mortality in rats.
Lin, Willie; Hsuan, Yogi Chang-Yo; Su, Yu-Chin; Lin, Cheng-Hsien; Lin, Mao-Tsun; Chen, Zi-Hao; Chang, Ching-Ping; Lin, Kao-Chang.
Afiliação
  • Lin W; Meridigen Biotech Co., Ltd., Taipei, Taiwan.
  • Hsuan YC; Meridigen Biotech Co., Ltd., Taipei, Taiwan.
  • Su YC; Meridigen Biotech Co., Ltd., Taipei, Taiwan.
  • Lin CH; Meridigen Biotech Co., Ltd., Taipei, Taiwan.
  • Lin MT; Department of Medical Research, Chi Mei Medical Center, Tainan, Taiwan.
  • Chen ZH; Institute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Chang CP; Department of Biotechnology, Southern Taiwan University of Science and Technology, Tainan, Taiwan.
  • Lin KC; Department of Medical Research, Chi Mei Medical Center, Tainan, Taiwan.
Oncotarget ; 9(2): 1992-2001, 2018 Jan 05.
Article em En | MEDLINE | ID: mdl-29416747
ABSTRACT
CD34 is a transmembrane phosphoglycoprotein used to selectively enrich bone marrow in hematopoietic stem cells for transplantation. Treating rats with CD34+ cells derived from human umbilical cord blood before or after heat stroke has been shown to promote survival. We investigated whether CD34- human placenta-derived stem cells (PDMSCs) could improve survival following heat stroke in rats. Rats were subjected to heat stress (42°C for 98 min) to induce heat stroke. Intravenous administration of PDMSCs 1 day before or immediately after the onset of heat stroke improved survival by 60% and 20%, respectively. Pre-treatment with CD34- PDMSCs protected against heat stroke injury more effectively than that treatment after injury. PDMSCs treatment attenuated cerebrovascular dysfunction, the inflammatory response, and lipid peroxidation. These data suggest human PDMSCs protect against heat stroke injury in rats. Moreover, these effects do not require the presence of CD34+ cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Taiwan