Hebb Adam O, Hebb Kari, Ramachandran Arun C, Mendez Ivar
Department of Anatomy, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
J Neurosurg. 2003 May;98(5):1078-83. doi: 10.3171/jns.2003.98.5.1078.
Transplantation of fetal dopaminergic tissue is being investigated in animal models and clinical trials for its potential as a treatment for advanced Parkinson disease. At the same time, the availability of fetal tissue is limited, making its storage time prior to transplantation a key practical issue. Although it results in a smaller percentage of surviving cells. a longer storage time enables fetal tissue obtained over several days to be pooled for transplantation in a recipient. Glial cell line-derived neurotrophic factor (GDNF) has been shown to improve survival of human dopaminergic tissue that has been stored prior to transplantation. The objective of this study was to evaluate the effects on fetal dopaminergic tissue of GDNF-supplemented hibernation for extended periods of 6 to 15 days.
The ventral mesencephalon (VM) was harvested in a total of 27 14-day-old rat fetuses, and three VMs were cultured immediately (fresh control group). The remaining 24 VMs were divided sagittally along the midline to yield 48 equal pieces of hemimesencephalon. Twenty-four pieces were stored with GDNF-supplemented hibernation medium for 6, 9, 12, or 15 days, and the 24 "partner" hemimesencephalon pieces were stored in control hibernation medium for the same periods of time. Tissue was cultured for 48 hours and processed for tyrosine hydroxylase (TH) immunoreactivity and double-stained with cresyl violet. Cell counts for all cultures and the percentage of TH-immunoreactive cells were obtained. The percentage of TH-immunoreactive cells for the fresh control group was 6.3 +/- 0.5%. The percentage of TH-immunoreactive cells in cultures derived from tissue stored in GDNF-supplemented medium was significantly increased at 6 and 9 days posthibernation compared with the fresh control group and the "partner" groups stored in hibernation medium only. No significant increase in the percentage of TH-immunoreactive cells was observed in the 12- and 15-day groups.
In this study the authors have demonstrated that fetal dopaminergic tissue can be safely stored for up to 9 days in GDNF-supplemented hibernation medium. Furthermore, the percentage of TH-immunoreactive cells is significantly increased after 6 and 9 days of storage in this medium, improving the yield of TH-immunoreactive cells prior to transplantation. These observations have practical clinical implications for collecting fetal dopaminergic cells and improving their survival after transplantation.
胎儿多巴胺能组织移植作为晚期帕金森病的一种潜在治疗方法正在动物模型和临床试验中进行研究。与此同时,胎儿组织的可用性有限,这使得其移植前的储存时间成为一个关键的实际问题。尽管储存时间延长会导致存活细胞的比例降低,但较长的储存时间能使数天内获取的胎儿组织集中起来用于受体移植。胶质细胞系源性神经营养因子(GDNF)已被证明可提高移植前储存的人多巴胺能组织的存活率。本研究的目的是评估补充GDNF的长时间(6至15天)冬眠对胎儿多巴胺能组织的影响。
总共从27只14日龄大鼠胎儿中获取腹侧中脑(VM),并立即培养3个VM(新鲜对照组)。将其余24个VM沿中线矢状切开,得到48个相等的半中脑片。24个半中脑片用补充GDNF的冬眠培养基储存6、9、12或15天,另外24个“配对”半中脑片用对照冬眠培养基在相同时间储存。组织培养48小时,进行酪氨酸羟化酶(TH)免疫反应处理并用甲酚紫进行双重染色。获得所有培养物的细胞计数以及TH免疫反应性细胞的百分比。新鲜对照组TH免疫反应性细胞的百分比为6.3±0.5%。与新鲜对照组和仅用冬眠培养基储存的“配对”组相比,在补充GDNF培养基中储存的组织来源培养物中,TH免疫反应性细胞的百分比在冬眠后6天和9天显著增加。在12天和15天组中未观察到TH免疫反应性细胞百分比的显著增加。
在本研究中,作者证明胎儿多巴胺能组织在补充GDNF的冬眠培养基中可安全储存长达9天。此外,在该培养基中储存6天和9天后,TH免疫反应性细胞的百分比显著增加,提高了移植前TH免疫反应性细胞的产量。这些观察结果对于收集胎儿多巴胺能细胞并提高其移植后的存活率具有实际临床意义。