Systemic human CD34+ cells populate the brain and activate host mechanisms to counteract nigrostriatal degeneration

被引：7

作者：

Corenblum, Mando J. ^{[1
]}

Flores, Andrew J. ^{[1
,2
]}

Badowski, Michael ^{[3
]}

Harris, David T. ^{[3
]}

Madhavan, Lalitha ^{[1
]}

机构：

[1] Univ Arizona, Dept Neurol, Tucson, AZ 85724 USA

[2] Univ Arizona, Physiol Sci Grad Program, Tucson, AZ 85724 USA

[3] Univ Arizona, Dept Immunobiol, Tucson, AZ 85724 USA

来源：

REGENERATIVE MEDICINE | 2015年 / 10卷 / 05期

关键词：

6-OHDA; angiogenesis; CD34(+) mononuclear cells; cord blood; neurogenesis; neuroprotection; Parkinson's disease; UMBILICAL-CORD BLOOD; MESENCHYMAL STROMAL CELLS; NEURAL STEM-CELLS; PARKINSONS-DISEASE; MOUSE MODEL; TISSUE-REPAIR; TRANSPLANTATION; STROKE; NEUROPROTECTION; RAT;

D O I：

10.2217/rme.15.32

中图分类号：

Q813 [细胞工程];

学科分类号：

100113 [医学细胞生物学];

摘要：

Aim: Here we investigated the neuroprotective potential of systemic CD34(+) human cord blood cells (hCBCs) in a 6-hydroxydopamine rat model of Parkinson's disease. Methods: Purified CD34(+) hCBCs were intravenously administered to rats subjected to 6-hydroxydopamine 24 h earlier, and behavioral and immunohistological analysis performed. Results: CD34(+) hCBC administration significantly prevented host nigrostriatal degeneration inducing behavioral recovery in treated rats. Although donor hCBCs did not differentiate into neural phenotypes, they stimulated the production of new neuroblasts and angiogenesis, and reduced gliosis in recipient animals. Importantly, surviving donor hCBCs were identified, and their tissue distribution pattern correlated with the observed therapeutic effects. Conclusion: Peripherally applied CD34(+) hCBCs can migrate into brain tissues and elicit host-based protective mechanisms to support the survival of midbrain dopamine neurons.

引用

页码：563 / 577

页数：15

共 44 条

[1]

Effects of intravenous human umbilical cord blood CD34+stem cell therapy versus levodopa in experimentally induced Parkinsonism in mice [J].