Nikkhah G, Cunningham M G, Jödicke A, Knappe U, Björklund A
Department of Medical Cell Research, University of Lund, Sweden.
Brain Res. 1994 Jan 7;633(1-2):133-43. doi: 10.1016/0006-8993(94)91532-6.
A microtransplantation approach has been used in order to achieve more complete reinnervation of the dopamine denervated rat striatum by fetal nigral cell suspensions injected into multiple striatal sites. A total of 450,000 cells, obtained from the ventral mesencephalon of embryonic day 14 rat fetuses, were implanted either in the conventional way as two 1.8-microliters deposits centrally in the head of the caudate-putamen ('Macro grafts'), or as eighteen 0.2-microliter deposits disseminated over six needle penetrations in the same area using a 50-70 microns glass capillary tip ('Micro grafts'). Non-grafted lesioned rats served as controls. Dopamine neuron survival (as assessed by tyrosine hydroxylase immunohistochemistry at 4 months after transplantation) was 2.8-fold greater in the Micro grafts as compared to the Macro grafts. Striatal dopamine tissue levels (determined in a separate group of rats) was increased 2.5-fold in the head of the caudate-putamen (from 12.5% of normal in the Macro graft group to 30% of normal in the Micro graft group). Consistent with this, the overall graft-derived tyrosine hydroxylase positive fiber outgrowth was more extensive in the Micro graft group and covered larger areas of the previously denervated caudate-putamen. The results show that distribution of the fetal nigral tissue in multiple small deposits provides for increased dopamine neuron survival, probably because of a closer contact between the implanted cells and the surrounding host striatal tissue in the small-sized graft deposits. Less bleeding and necrosis at the implantation site may also have contributed to this effect. The present microtransplantation procedure is an efficient means to increase overall dopamine neuron survival and to achieve more complete reinnervation of the denervated striatum in the rat Parkinson model. It also substantially increased the reproducibility of DA graft survival between animals.
为了通过将胎儿黑质细胞悬液注射到多个纹状体部位,使多巴胺去神经支配的大鼠纹状体获得更完全的再支配,已采用了一种微移植方法。从胚胎第14天大鼠胎儿的腹侧中脑获得总共450,000个细胞,以常规方式植入,即作为两个1.8微升的沉积物集中在尾状核 - 壳核头部中央(“大移植”),或者作为18个0.2微升的沉积物,使用50 - 70微米的玻璃毛细管尖端在同一区域的六个针道中分散植入(“微移植”)。未移植的损伤大鼠作为对照。与大移植相比,微移植中多巴胺神经元的存活率(移植后4个月通过酪氨酸羟化酶免疫组织化学评估)高2.8倍。尾状核 - 壳核头部的纹状体多巴胺组织水平(在另一组大鼠中测定)增加了2.5倍(从大移植组中正常水平的12.5%增加到微移植组中正常水平的30%)。与此一致的是,微移植组中来自移植物的酪氨酸羟化酶阳性纤维的总体生长更广泛,覆盖了先前去神经支配的尾状核 - 壳核的更大区域。结果表明,胎儿黑质组织分布在多个小沉积物中可提高多巴胺神经元的存活率,这可能是因为在小尺寸移植沉积物中植入的细胞与周围宿主纹状体组织之间的接触更紧密。植入部位较少的出血和坏死也可能促成了这种效果。目前的微移植程序是提高多巴胺神经元总体存活率以及在大鼠帕金森模型中实现去神经支配纹状体更完全再支配的有效方法。它还大大提高了动物之间多巴胺移植物存活的可重复性。