Guthrie Kathleen M, Tran Amy, Baratta Janie, Yu Jen, Robertson Richard T
Department of Anatomy and Neurobiology, College of Medicine, University of California, Irvine, CA 92697-1280, USA.
Brain Res Dev Brain Res. 2005 Jun 30;157(2):162-71. doi: 10.1016/j.devbrainres.2005.04.002.
Cholinergic axons originating from the septum form a characteristic layer of preterminal axons and apparent termination in the molecular layer of the hippocampal dentate gyrus. The present study explored the specificity of this characteristic axonal pattern, through the use of organotypic slice co-cultures. Slices of hippocampus were co-cultured with a slice from one of a variety of other potential sources of afferents, and the afferent axons were labeled histochemically or immunocytochemically to determine which afferents distribute within the dentate molecular layer in a pattern similar to that formed by septal cholinergic projections. Acetylcholinesterase (AChE) histochemistry demonstrated that cholinergic axons from septum, substantia innominata, and striatum all consistently targeted the inner molecular layer of the dentate gyrus. AChE-labeled cholinergic axons from dorsal lateral pontine tegmentum and from spinal cord sometimes formed this pattern, while axons from the habenula failed to extend into the dentate gyrus. Immunocytochemically identified monoaminergic axons from the substantia nigra, locus coeruleus, and raphe extended into co-cultured hippocampus; each of these afferent systems displayed a prominent axonal plexus within the hilus of the dentate, but only the raphe axons projected prominently to the molecular layer. These data demonstrate that the molecular layer of the dentate gyrus provides an attractive target zone for some cholinergic and monoaminergic afferents, but not all. Commonalities between neuronal populations that preferentially project to the molecular layer in vitro may offer clues regarding the axon guidance mechanisms that normally direct cholinergic axons to target sites in the dentate gyrus molecular layer.
源自隔区的胆碱能轴突在海马齿状回分子层形成特征性的终末前轴突层和明显的终末。本研究通过使用器官型脑片共培养来探究这种特征性轴突模式的特异性。将海马脑片与来自多种其他潜在传入源之一的脑片进行共培养,并用组织化学或免疫细胞化学方法标记传入轴突,以确定哪些传入纤维以类似于隔区胆碱能投射形成的模式分布在齿状分子层内。乙酰胆碱酯酶(AChE)组织化学显示,来自隔区、无名质和纹状体的胆碱能轴突始终靶向齿状回的内分子层。来自背外侧脑桥被盖和脊髓的AChE标记胆碱能轴突有时形成这种模式,而来自缰核的轴突未能延伸至齿状回。免疫细胞化学鉴定的来自黑质、蓝斑和中缝核的单胺能轴突延伸至共培养的海马中;这些传入系统中的每一个在齿状回的 hilus内都显示出一个突出的轴突丛,但只有中缝核的轴突显著投射到分子层。这些数据表明,齿状回分子层为一些胆碱能和单胺能传入纤维提供了一个有吸引力的靶区,但并非全部。在体外优先投射到分子层的神经元群体之间的共性可能为正常情况下将胆碱能轴突引导至齿状回分子层靶位点的轴突导向机制提供线索。