Neuroprotective effect of a cell-free extract derived from human adipose stem cells in experimental stroke models

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• 作者：Daejong Jeon^a ; ¹ ; ^{clark@kaist.ac.kr} ; Kon Chu^b ; ¹ ; Soon-Tae Lee^b ; ¹ ; Keun-Hwa Jung^b ; Jae-Jun Ban^b ; Dong-Kyu Park^b ; Hye-Jin Yoon^b ; Seungmoon Jung^a ; Hyunwoo Yang^a ; Byung Sun Kim^a ; Ji Ye Choi^a ; So Hee Kim^b ; Jeong-Min Kim^b ; Chong-Hyun Won^c ; Manho Kim^b ; Sang Kun Lee^b ; Jae-Kyu Roh^b ; ^{rohjk@snu.ac.kr}
• 关键词：hASCs-E ; extract of human adipose stem cell ; OGD ; oxygen and glucose deprivation ; MCA ; middle cerebral artery ; ICH ; intracerebral hemorrhage ; LDH ; lactate dehydrogenase
• 刊名：Neurobiology of Disease
• 出版年：2013
• 出版时间：June, 2013
• 年：2013
• 卷：54
• 期：Complete
• 页码：414-420
• 全文大小：877 K

文摘

A recent study suggested that a cell-free extract of human adipose stem cells (hASCs-E) has beneficial effects on neurological diseases by modulating the host environment. Here, we investigated the effects of hASCs-E in several experimental models of stroke in vitro (oxygen and glucose deprivation, OGD) and in vivo (transient or permanent focal cerebral ischemia and intracerebral hemorrhage, ICH). Ischemia was induced in vitro in Neuro2A cells, and the hASCs-E was applied 24 h before the OGD or concurrently. Focal cerebral ischemia was induced by unilateral intraluminal thread occlusion of the middle cerebral artery (MCA) in rats for 90 min or permanently, or by unilateral MCA microsurgical direct electrocoagulation in mice. The ICH model was induced with an intracerebral injection of collagenase in rats. The hASCs-E was intraperitoneally administered 1 h after the stroke insults. Treatment of the hASCs-E led to a substantially high viability in the lactate dehydrogenase and WST-1 assays in the in vitro ischemic model. The cerebral ischemic and ICH model treated with hASCs-E showed decreased ischemic volume and reduced brain water content and hemorrhage volume. The ICH model treated with hASCs-E exhibited better performance on the modified limb placing test. The expression of many genes related to inflammation, immune response, and cell-death was changed substantially in the ischemic rats or neuronal cells treated with the hASCs-E. These results reveal a neuroprotective role of hASCs-E in animal models of stroke, and suggest the feasible application of stem cell-based, noninvasive therapy for treating stroke.