Dailey M E, Buchanan J, Bergles D E, Smith S J
Department of Molecular and Cellular Physiology, Stanford University School of Medicine, California 94305-5426.
J Neurosci. 1994 Mar;14(3 Pt 1):1060-78. doi: 10.1523/JNEUROSCI.14-03-01060.1994.
Hippocampal slices from early postnatal rat were used to study mossy fiber (MF) growth and synaptogenesis. The ability of MFs to form new giant synapses within isolated tissue slices was established by a series of experiments involving synapsin I immunohistochemistry, electron microscopy, and whole-cell recordings. When hippocampal slices from immature rats were cultured for up to 2 weeks, the distribution of giant MF terminals was similar to that found in vivo. Using a lesioning procedure, we determined that MFs in slices extend and form appropriate synaptic connections with normal target CA3 pyramidal cells. MF terminals were dispersed more widely than normal within the CA3 pyramidal layer after a lesion, but electron microscopy indicated that synaptic junctions were still primarily associated with pyramidal cell dendrites and not the somata. Establishment of functional synaptic input in vitro was confirmed by whole-cell recordings of MF-driven excitatory postsynaptic currents (50 pA to 1 nA) in pyramidal cells. The results establish for the first time that an MF projection with appropriate and functional synaptic connections can be formed de novo and not just maintained in excised hippocampal slices. The cellular dynamics underlying MF growth and synaptogenesis were examined directly by time-lapse confocal imaging of fibers selectively stained with a fluorescent membrane dye (Dil or DiO). MFs growing deep within isolated tissue slices were tipped by small (5-10 microns), active growth cones that advanced at variable rates (5-25 microns/hr). Furthermore, dynamic filopodial structures were seen at small varicosities along the length of developing MFs, which may identify nascent en passant synaptic contacts. The hippocampal slice preparations are shown to support normal development of MF connections and allow for direct visualization of the cellular dynamics of synapse formation in a mammalian CNS tissue environment.
出生后早期大鼠的海马切片被用于研究苔藓纤维(MF)的生长和突触形成。通过一系列涉及突触素I免疫组织化学、电子显微镜和全细胞记录的实验,确定了MF在分离的组织切片内形成新的巨型突触的能力。当将未成熟大鼠的海马切片培养长达2周时,巨型MF终末的分布与体内发现的相似。通过损伤程序,我们确定切片中的MF会延伸并与正常的靶CA3锥体细胞形成适当的突触连接。损伤后,MF终末在CA3锥体细胞层内的分布比正常情况更广泛,但电子显微镜显示突触连接仍主要与锥体细胞树突而非胞体相关。通过对锥体细胞中MF驱动的兴奋性突触后电流(50 pA至1 nA)进行全细胞记录,证实了体外功能性突触输入的建立。这些结果首次证明,具有适当且功能性突触连接的MF投射可以从头形成,而不仅仅是在切除的海马切片中维持。通过用荧光膜染料(Dil或DiO)选择性染色纤维的延时共聚焦成像,直接检查了MF生长和突触形成的细胞动力学。在分离的组织切片深处生长的MF由小的(5 - 10微米)、活跃的生长锥所引导,这些生长锥以可变速率(5 - 25微米/小时)前进。此外,在发育中的MF长度上的小曲张处可见动态丝状伪足结构,这可能识别新生的过路突触接触。海马切片制备显示支持MF连接的正常发育,并允许在哺乳动物中枢神经系统组织环境中直接观察突触形成的细胞动力学。