Fawcett J W, Barker R A, Dunnett S B
MRC Cambridge Centre for Brain Repair, University of Cambridge, England.
Exp Brain Res. 1995;106(2):275-82. doi: 10.1007/BF00241123.
Embryonic substantia nigra cells when transplanted into the striatum can reverse many of the defects of Parkinson's disease. The efficacy of such grafts is compromised by the poor survival of grafted dopaminergic neurones; typically, 3-10% survive transplantation. We used three tissue culture models to identify stages in the procedure for the preparation and insertion of grafts which might be responsible for this cell death and to identify environments in which survival is optimised. (1) The ventral mesencephalon was dissected from the donor brain, then placed immediately into culture contained in a collagen gel. (2) The dissected tissue fragments were enzymatically dissociated, then the cells placed into monolayer culture. (3) Enzymatically dissociated tissue was packed into 0.5-mm-diameter porous tubes, to simulate the compaction of cells into a graft deposit in the host brain. Dissociation of the tissue by itself caused the death of approximately 30% of dopaminergic neurones, as judged by the difference in cell counts between the intact embryonic day 14 (E14) mesencephalon, and cells dissociated then packed into tubes. Of the dissociated neurones approximately 60% died during the first 24 h and 87% during the first 3 days in monolayer culture, while only 7% of dopaminergic neurones in three-dimensional cultures and 11% of neurones in explant cultures died over the first 3 days. Embryonic dopaminergic neurones are clearly very vulnerable to adverse conditions during the first days after their removal from the donor brain. The excellent survival of neurones in three-dimensional and explant cultures indicates that close association with other cells, which may provide greatly improved access to trophic factors, can enable the cells to survive this period of vulnerability. In contrast to its effects in monolayer cultures, bFGF had no effect on dopaminergic neuronal survival in either explant or three-dimensional cultures.
胚胎黑质细胞移植到纹状体后可逆转帕金森病的许多缺陷。然而,移植的多巴胺能神经元存活率低影响了这种移植的疗效;通常,只有3% - 10%的移植神经元能够存活。我们使用了三种组织培养模型来确定移植准备和植入过程中可能导致这种细胞死亡的阶段,并确定能使细胞存活率达到最优的环境。(1)从供体脑中取出腹侧中脑,然后立即置于胶原凝胶包裹的培养环境中。(2)将解剖后的组织碎片进行酶解,然后将细胞置于单层培养。(3)将酶解后的组织填充到直径0.5毫米的多孔管中,以模拟细胞在宿主脑中聚集成移植沉积物的过程。根据完整的胚胎第14天(E14)中脑与酶解后装入管中的细胞数量差异判断,单纯组织解离会导致约30%的多巴胺能神经元死亡。在单层培养中,约60%的解离神经元在最初24小时内死亡,87%在最初3天内死亡,而在三维培养中,最初3天内只有7%的多巴胺能神经元死亡,在外植体培养中为11%。胚胎多巴胺能神经元在从供体脑取出后的最初几天显然极易受到不利条件的影响。神经元在三维培养和外植体培养中的良好存活率表明,与其他细胞紧密结合,可能极大地改善对营养因子的获取,能使细胞在这一脆弱期存活下来。与在单层培养中的作用不同,碱性成纤维细胞生长因子(bFGF)在外植体培养或三维培养中对多巴胺能神经元的存活均无影响。