Yu W, Centonze V E, Ahmad F J, Baas P W
Department of Anatomy, University of Wisconsin Medical School, Madison 53706.
J Cell Biol. 1993 Jul;122(2):349-59. doi: 10.1083/jcb.122.2.349.
We have proposed that microtubules (MTs) destined for axons and dendrites are nucleated at the centrosome within the cell body of the neuron, and are then released for translocation into these neurites (Baas, P. W., and H. C. Joshi. 1992. J. Cell Biol. 119:171-178). In the present study, we have tested the capacity of the neuronal centrosome to act as a generator of MTs for relocation into other regions of the neuron. In cultured sympathetic neurons undergoing active axonal outgrowth, MTs are present throughout the cell body including the region around the centrosome, but very few (< 10) are directly attached to the centrosome. These results indicate either that the neuronal centrosome is relatively inactive with regard to MT nucleation, or that most of the MTs nucleated at the centrosome are rapidly released. Treatment for 6 h with 10 micrograms/ml nocodazole results in the depolymerization of greater than 97% of the MT polymer in the cell body. Within 5 min after removal of the drug, hundreds of MTs have assembled in the region of the centrosome, and most of these MTs are clearly attached to the centrosome. A portion of the MTs are not attached to the centrosome, but are aligned side-by-side with the attached MTs, suggesting that the unattached MTs were released from the centrosome after nucleation. In addition, unattached MTs are present in the cell body at decreasing levels with increasing distance from the centrosome. By 30 min, the MT array of the cell body is indistinguishable from that of controls. The number of MTs attached to the centrosome is once again diminished to fewer than 10, suggesting that the hundreds of MTs nucleated from the centrosome after 5 min were subsequently released and translocated away from the centrosome. These results indicate that the neuronal centrosome is a highly potent MT-nucleating structure, and provide strong indirect evidence that MTs nucleated from the centrosome are released for translocation into other regions of the neuron.
我们曾提出,去往轴突和树突的微管(MTs)在神经元胞体内的中心体处成核,然后被释放以便转运至这些神经突中(巴斯,P. W.,以及H. C. 乔希。1992年。《细胞生物学杂志》119:171 - 178)。在本研究中,我们测试了神经元中心体作为MTs生成器以重新定位到神经元其他区域的能力。在正在进行活跃轴突生长的培养交感神经元中,MTs存在于整个胞体,包括中心体周围区域,但直接附着于中心体的MTs非常少(<10个)。这些结果表明,要么神经元中心体在MT成核方面相对不活跃,要么在中心体处成核的大多数MTs会迅速被释放。用10微克/毫升诺考达唑处理6小时会导致胞体中超过97%的MT聚合物解聚。在去除药物后的5分钟内,数百个MTs在中心体区域组装,并且这些MTs中的大多数明显附着于中心体。一部分MTs未附着于中心体,但与附着的MTs并排排列,这表明未附着的MTs在成核后从中心体释放。此外,未附着的MTs在胞体中的水平随着与中心体距离的增加而降低。到30分钟时,胞体的MT阵列与对照组的难以区分。附着于中心体的MTs数量再次减少至少于10个,这表明5分钟后从中心体成核的数百个MTs随后被释放并从中心体转运离开。这些结果表明,神经元中心体是一种高效的MT成核结构,并提供了有力的间接证据,证明从中心体成核的MTs被释放以便转运至神经元的其他区域。