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通过胶质细胞移植实现犬中枢神经系统的髓鞘形成:一种人类髓鞘疾病修复模型

Myelination of the canine central nervous system by glial cell transplantation: a model for repair of human myelin disease.

作者信息

Archer D R, Cuddon P A, Lipsitz D, Duncan I D

机构信息

Department of Pediatrics, Emory University, Atlanta, Georgia 30322, USA.

出版信息

Nat Med. 1997 Jan;3(1):54-9. doi: 10.1038/nm0197-54.

Abstract

There is a lack of effective means of promoting remyelination of the central nervous system (CNS) in humans with chronic demyelinating disease. We have investigated the ability of transplanted glia to myelinate areas of the CNS equivalent to focal demyelinated lesions in multiple sclerosis (MS). In these studies we show that transplantation of oligodendrocytes or their progenitors into the CNS of a neonatal or adult canine myelin mutant results in repair of large areas similar in size to many MS plaques. Progenitor or pre-progenitor cells of the oligodendrocyte lineage have the greatest capacity for myelination following grafting, although cells of neonatal origin may also be used. Such an approach may therefore have therapeutic value in the repair of focal lesions in human myelin disease.

摘要

对于患有慢性脱髓鞘疾病的人类,缺乏促进中枢神经系统(CNS)髓鞘再生的有效手段。我们研究了移植神经胶质细胞对中枢神经系统中相当于多发性硬化症(MS)局灶性脱髓鞘病变区域进行髓鞘形成的能力。在这些研究中,我们表明将少突胶质细胞或其祖细胞移植到新生或成年犬髓磷脂突变体的中枢神经系统中,可修复面积与许多MS斑块大小相似的大面积区域。少突胶质细胞谱系的祖细胞或前祖细胞在移植后具有最大的髓鞘形成能力,尽管也可以使用新生来源的细胞。因此,这种方法可能对人类髓磷脂疾病局灶性病变的修复具有治疗价值。

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