Sergaki Maria Christina, López-Ramos Juan Carlos, Stagkourakis Stefanos, Gruart Agnès, Broberger Christian, Delgado-García José María, Ibáñez Carlos F
Department of Neuroscience, Karolinska Institute, Stockholm S-17177, Sweden.
Division of Neurosciences, Pablo de Olavide University, Seville 41013, Spain.
Cell Rep. 2017 Jun 6;19(10):1977-1986. doi: 10.1016/j.celrep.2017.05.030.
The role of neurotrophic factors as endogenous survival proteins for brain neurons remains contentious. In the cerebellum, the signals controlling survival of molecular layer interneurons (MLIs) are unknown, and direct evidence for the requirement of a full complement of MLIs for normal cerebellar function and motor learning has been lacking. Here, we show that Purkinje cells (PCs), the target of MLIs, express the neurotrophic factor GDNF during MLI development and survival of MLIs depends on GDNF receptors GFRα1 and RET. Conditional mutant mice lacking either receptor lose a quarter of their MLIs, resulting in compromised synaptic inhibition of PCs, increased PC firing frequency, and abnormal acquisition of eyeblink conditioning and vestibulo-ocular reflex performance, but not overall motor activity or coordination. These results identify an endogenous survival mechanism for MLIs and reveal the unexpected vulnerability and selective requirement of MLIs in the control of cerebellar-dependent motor learning.
神经营养因子作为脑神经元内源性存活蛋白的作用仍存在争议。在小脑中,控制分子层中间神经元(MLIs)存活的信号尚不清楚,并且缺乏关于正常小脑功能和运动学习需要完整数量的MLIs的直接证据。在这里,我们表明,作为MLIs靶标的浦肯野细胞(PCs)在MLIs发育过程中表达神经营养因子GDNF,且MLIs的存活依赖于GDNF受体GFRα1和RET。缺乏任一受体的条件性突变小鼠会损失四分之一的MLIs,导致PCs的突触抑制受损、PCs放电频率增加、眨眼条件反射和前庭眼反射表现的异常习得,但总体运动活动或协调性未受影响。这些结果确定了MLIs的一种内源性存活机制,并揭示了MLIs在小脑依赖性运动学习控制中的意外脆弱性和选择性需求。