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首页> 外文期刊>The Journal of Physiology >TrkB is necessary for pruning at the climbing fibre-Purkinje cell synapse in the developing murine cerebellum.
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TrkB is necessary for pruning at the climbing fibre-Purkinje cell synapse in the developing murine cerebellum.

机译:TrkB对于修剪正在发育的鼠小脑中的攀爬纤维-Purkinje细胞突触是必需的。

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摘要

TrkB, the cognate receptor for brain-derived neurotrophic factor and neurotrophin-4, has been implicated in regulating synapse formation in the central nervous system. Here we asked whether TrkB plays a role in the maturation of the climbing fibre-Purkinje cell (CF-PC) synapse. In rodent cerebellum, Purkinje cells are initially innervated by multiple climbing fibres that are subsequently culled to assume the mature mono-innervated state, and whose contacts translocate from the soma to the dendrites. By employing transgenic mice hypomorphic or null for TrkB expression, our results indicated that perturbation of TrkB in the immature cerebellum resulted in ataxia, that Purkinje cells remained multiply innervated by climbing fibres beyond the normal developmental time frame, and that synaptic transmission at the parallel fibre-Purkinje cell synapse remained functionally unaltered. Mechanistically, we present evidence that attributes the persistence of multiple climbing fibre innervation to an obscured discrimination of relative strengths among competing climbing fibres. Soma-to-dendrite translocation of climbing fibre terminals was unaffected. Thus, TrkB regulates pruning but not translocation of nascent CF-PC synaptic contacts.
机译:TrkB是脑源性神经营养因子和Neurotrophin-4的同源受体,已参与调节中枢神经系统的突触形成。在这里,我们问TrkB是否在攀登纤维Purkinje细胞(CF-PC)突触的成熟中起作用。在啮齿类动物小脑中,浦肯野细胞最初由多条攀爬纤维支配,随后被剔除以呈现成熟的单神经支配状态,并且其接触点从体细胞转移至树突。通过对TrkB表达采用亚型或无效的转基因小鼠,我们的结果表明,未成熟小脑中的TrkB紊乱导致共济失调,浦肯野细胞仍然通过攀爬纤维超出正常发育时间而受多个神经支配,并且突触传递在平行纤维上-Purkinje细胞突触的功能保持不变。从机理上讲,我们提供的证据将多重攀爬纤维神经支配的持久性归因于竞争性攀爬纤维之间相对强度的模糊区分。攀登纤维末端的索玛向树突移位不受影响。因此,TrkB调节修剪,但不调节新生CF-PC突触接触的易位。

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