Hsiang J, Price S D, Heller A, Hoffmann P C, Wainer B H
Department of Pathology, University of Chicago, IL 60637.
Neuroscience. 1988 Aug;26(2):417-31. doi: 10.1016/0306-4522(88)90159-5.
We have previously demonstrated at the light microscopic level that when embryonic day-15 septal neurons are co-cultured for 21 days with their target cells from the hippocampus, increased numbers of septal cholinergic neurons are present as compared with co-cultures employing cells from the non-target cerebellum. In addition, fine varicose axon-like cholinergic fibers are found to be associated with the hippocampal cells but not with cerebellar cells. We now provide ultrastructural evidence for hippocampal target cell-enhanced cholinergic neuronal survival, axonal proliferation, and synapse formation in this culture system. Dissociated cell suspensions from septal, hippocampal, and cerebellar areas were obtained from 15-day mouse embryos; and hippocampal and cerebellar cells were internally labeled with rhodamine-conjugated wheat germ agglutinin. Combinations of septal and hippocampal cells, and septal and cerebellar cells were allowed to reaggregate in rotation mediated culture for either 15 or 21 days. The reaggregates were then fixed, embedded, sectioned, and processed for acetylcholinesterase-positive acetylcholinesterase-positive cells and fibers, and under fluorescence to locate rhodamine-labeled cell populations. Representative reaggregate profiles were then re-embedded for electron microscopic examination. In both types of reaggregates, either labeled hippocampal target or cerebellar non-target cells segregated from the septal cells so that areas containing each of the respective cell populations could be studied. In sections of septal-hippocampal reaggregates from 15-day cultures, 571 out of 665 (85%) cholinergic neurons examined were intact, whereas 15% of the cells showed some ultrastructural features of degeneration. Similarly, at day 21, 297 out of 335 (88%) of the cholinergic neurons were intact. In sections of septal-cerebellar reaggregates from 15-day cultures, 473 out of 572 (83%) cholinergic neurons were intact. By day 21 of culture, however, only 15 out of 110 (14%) cholinergic neurons examined were intact from the septal-cerebellar reaggregates. In areas of septal-hippocampal reaggregates occupied by rhodamine-labeled hippocampal cells, profiles of acetylcholinesterase-labeled axons were identified, and synaptic specializations were observed between cholinergic terminals and dendrites as well as somata of hippocampal target cells. In contrast, areas of septal-cerebellar reaggregates occupied by rhodamine-labeled cerebellar cells were devoid of cholinergic fibers.(ABSTRACT TRUNCATED AT 400 WORDS)
我们之前已在光学显微镜水平证实,当胚胎第15天的隔区神经元与来自海马体的靶细胞共培养21天时,与采用来自非靶组织小脑的细胞进行共培养相比,隔区胆碱能神经元数量增加。此外,发现纤细的曲张状轴突样胆碱能纤维与海马体细胞相关联,而与小脑细胞无关联。我们现在提供超微结构证据,证明在该培养系统中海马体靶细胞可增强胆碱能神经元存活、轴突增殖及突触形成。从15日龄小鼠胚胎获取隔区、海马体及小脑区域的解离细胞悬液;并用罗丹明偶联的麦胚凝集素对海马体和小脑细胞进行内标记。将隔区与海马体细胞的组合,以及隔区与小脑细胞的组合在旋转介导培养中重新聚集15天或21天。然后将重新聚集物固定、包埋、切片,并进行乙酰胆碱酯酶阳性细胞和纤维处理,以及在荧光下定位罗丹明标记的细胞群体。然后将代表性的重新聚集物轮廓重新包埋以进行电子显微镜检查。在两种类型的重新聚集体中,标记的海马体靶细胞或小脑非靶细胞均与隔区细胞分离,从而可以研究包含各自细胞群体的区域。在15天培养的隔区 - 海马体重新聚集体切片中,所检查的665个胆碱能神经元中有571个(85%)完整,而15%的细胞显示出一些变性的超微结构特征。同样,在第21天,335个胆碱能神经元中有297个(88%)完整。在15天培养的隔区 - 小脑重新聚集体切片中,572个胆碱能神经元中有473个(83%)完整。然而,到培养第21天时,在隔区 - 小脑重新聚集体中所检查的110个胆碱能神经元中只有15个(14%)完整。在罗丹明标记的海马体细胞占据的隔区 - 海马体重新聚集体区域中,鉴定出乙酰胆碱酯酶标记的轴突轮廓,并观察到胆碱能终末与海马体靶细胞的树突以及胞体之间的突触特化。相比之下,罗丹明标记的小脑细胞占据的隔区 - 小脑重新聚集体区域没有胆碱能纤维。(摘要截于400字)