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受体酪氨酸磷酸酶之间的竞争与合作控制果蝇运动神经元生长锥的导向。

Competition and cooperation among receptor tyrosine phosphatases control motoneuron growth cone guidance in Drosophila.

作者信息

Desai C J, Krueger N X, Saito H, Zinn K

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125, USA.

出版信息

Development. 1997 May;124(10):1941-52. doi: 10.1242/dev.124.10.1941.

Abstract

The neural receptor tyrosine phosphatases DPTP69D, DPTP99A and DLAR are involved in motor axon guidance in the Drosophila embryo. Here we analyze the requirements for these three phosphatases in growth cone guidance decisions along the ISN and SNb motor pathways. Any one of the three suffices for the progression of ISN pioneer growth cones beyond their first intermediate target in the dorsal muscle field. DLAR or DPTP69D can facilitate outgrowth beyond a second intermediate target, and DLAR is uniquely required for formation of a normal terminal arbor. A different pattern of partial redundancy among the three phosphatases is observed for the SNb pathway. Any one of the three suffices to allow SNb axons to leave the common ISN pathway at the exit junction. When DLAR is not expressed, however, SNb axons sometimes bypass their ventrolateral muscle targets after leaving the common pathway, instead growing out as a separate bundle adjacent to the ISN. This abnormal guidance decision can be completely suppressed by also removing DPTP99A, suggesting that DLAR turns off or counteracts a DPTP99A signal that favors the bypass axon trajectory. Our results show that the relationships among the tyrosine phosphatases are complex and dependent on cellular context. At growth cone choice points along one nerve, two phosphatases cooperate, while along another nerve these same phosphatases can act in opposition to one another.

摘要

神经受体酪氨酸磷酸酶DPTP69D、DPTP99A和DLAR参与果蝇胚胎中的运动轴突导向。在此,我们分析了这三种磷酸酶在沿ISN和SNb运动通路的生长锥导向决策中的需求。这三种磷酸酶中的任何一种都足以使ISN先驱生长锥在背侧肌场中超越其第一个中间靶点。DLAR或DPTP69D可以促进生长锥超越第二个中间靶点,而正常终末分支的形成则唯一需要DLAR。在SNb通路中观察到三种磷酸酶之间存在不同的部分冗余模式。这三种磷酸酶中的任何一种都足以使SNb轴突在出口连接处离开共同的ISN通路。然而,当不表达DLAR时,SNb轴突有时在离开共同通路后会绕过其腹外侧肌肉靶点,而是作为与ISN相邻的单独一束生长。通过同时去除DPTP99A可以完全抑制这种异常的导向决策,这表明DLAR关闭或抵消了有利于旁路轴突轨迹的DPTP99A信号。我们的结果表明,酪氨酸磷酸酶之间的关系很复杂,并且取决于细胞环境。在一条神经的生长锥选择点处,两种磷酸酶相互协作,而在另一条神经上,这些相同的磷酸酶可能会相互拮抗。

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