Kawaja M D, Gage F H
Department of Neurosciences, University of California, San Diego, La Jolla 92093-0624.
J Comp Neurol. 1992 Mar 1;317(1):102-16. doi: 10.1002/cne.903170108.
In order to assess the feasibility of using primary skin fibroblasts as a donor population for genetic modification and subsequent intracerebral grafting, the present study examines the structural and neurochemical characteristics of intrastriatal grafts of isogeneic primary fibroblasts over a period of 6 months. In culture, primary skin fibroblasts obtained from a female Fischer 344 rat display robust growth, but once confluent these cells exhibit contact inhibition. Following the implantation of cultured primary cells within the striatum of other adult rats from the same inbred strain, isologous grafts stain immunohistochemically for fibronectin at 1 week, and this immunostaining persists up to 6 months. Immunoreactivity for laminin is intense within the grafts from 1 to 8 weeks, but decreases by 6 months. Astrocytes within the striatum respond dramatically to the implantation of primary fibroblasts, such that immunohistochemical staining for glial fibrillary acidic protein increases markedly from 1 to 8 weeks after implantation. Although the intensity of immunostaining for glial fibrillary acidic protein diminishes among striatal astrocytes between 8 weeks and 6 months, the astrocytic border between the grafts and striatal neuropil remains intensely immunoreactive. Capillaries within the grafts stain immunohistochemically for glucose transporter (a facilitated glucose uptake carrier) as early as 3 weeks after implantation. Following intravenous infusions of peroxidase, capillaries within fibroblast grafts do not permit the extravasation of this macromolecule at 8 weeks and 6 months. Thus, capillaries formed within intracerebral grafts of primary skin fibroblasts exhibit a functional impermeable barrier to macromolecules similar to those capillaries of the host striatum. At the ultrastructural level, grafts possess numerous fibroblasts and have an extracellular matrix filled with collagen. Reactive astrocytic processes filled with intermediate filaments are found throughout the grafts. Hypertrophied astrocytes and their processes also appear to form a continuous border between the grafts and striatal neuropil. Grafts of primary fibroblasts also possess an extensive vasculature that is composed of capillaries with nonfenestrated endothelial cells; the occurrence of reactive astrocytic processes closely associated with or enveloping capillaries is variable. These results provide direct morphological and neurochemical evidence for the long-term survival of isologous fibroblasts after implantation within the rat striatum. From these data, we propose that isologous skin fibroblasts can be considered as donor candidates for successful intracerebral grafting following gene transfer.
为了评估将原代表皮成纤维细胞作为基因修饰及随后脑内移植的供体细胞群的可行性,本研究检测了同基因原代成纤维细胞纹状体内移植6个月期间的结构和神经化学特征。在培养过程中,从雌性Fischer 344大鼠获取的原代表皮成纤维细胞生长旺盛,但一旦汇合,这些细胞即表现出接触抑制。将培养的原代细胞植入来自同一近交系的其他成年大鼠纹状体内后,同种异体移植物在1周时免疫组化染色显示纤维连接蛋白阳性,且这种免疫染色持续至6个月。层粘连蛋白的免疫反应性在移植物内1至8周时较强,但至6个月时减弱。纹状体内的星形胶质细胞对原代成纤维细胞的植入反应强烈,植入后1至8周,胶质纤维酸性蛋白的免疫组化染色显著增加。尽管纹状体星形胶质细胞内胶质纤维酸性蛋白的免疫染色强度在8周与6个月之间有所减弱,但移植物与纹状体神经毡之间的星形胶质细胞边界仍保持强烈的免疫反应性。移植物内的毛细血管早在植入后3周即免疫组化染色显示葡萄糖转运体(一种易化葡萄糖摄取载体)阳性。静脉注射过氧化物酶后,成纤维细胞移植物内的毛细血管在8周和6个月时均不允许该大分子外渗。因此,原代表皮成纤维细胞脑内移植物内形成的毛细血管对大分子表现出与宿主纹状体毛细血管类似的功能性不透性屏障。在超微结构水平,移植物含有大量成纤维细胞,并有充满胶原的细胞外基质。整个移植物内均可见充满中间丝的反应性星形胶质细胞突起。肥大的星形胶质细胞及其突起似乎也在移植物与纹状体神经毡之间形成了连续的边界。原代成纤维细胞移植物还拥有广泛的血管系统,由具有非窗孔状内皮细胞的毛细血管组成;与毛细血管紧密相关或包绕毛细血管的反应性星形胶质细胞突起的出现情况不一。这些结果为同种异体成纤维细胞植入大鼠纹状体后的长期存活提供了直接的形态学和神经化学证据。基于这些数据,我们提出同种异体皮肤成纤维细胞可被视为基因转移后成功进行脑内移植的供体候选细胞。