MICROTUBULES AND MICROFILAMENTS IN NEWT NEURULATION
MICROTUBULES AND MICROFILAMENTS IN NEWT NEURULATION
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DOI:
10.1016/0012-1606(71)90073-x
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发表时间:
1971-01-01
影响因子:
2.7
通讯作者:
BURNSIDE, B
中科院分区:
文献类型:
--
作者:
BURNSIDE, B
During urodele neurulation, presumptive neural cells elongate to form the neural plate and then constrict apically as the plate rolls up to form the neural tube. During the same period, epidermal cells gradually flatten. Electron microscopy of these cells has been carried out in an attempt to understand the mechanism of morphogenetic cell shape changes. In elongating neural plate cells, microtubules are oriented parallel to the long axis. Counts of numbers of these “paraxial” microtubules per cell do not differ significantly at three apicobasal levels of the cells; therefore, it is practical to consider the paraxial microtubules as a single population of full-cell-length microtubules. The number of paraxial microtubules per cell decreases significantly as the cell elongates, but the degree of elongation of a cell at a given stage is not closely related to the number of paraxial microtubules it contains. Several observations suggest that microtubules contribute to cell elongation by some form of transport mechanism. During the apical constriction of neural ectoderm cells, there is marked increase in thickness of a circumferential bundle of microfilaments which encircles the cell apex. The inverse relationship between increase in bundle thickness and decrease in circumference of the cell apex suggests that these processes result from increased overlap and interdigitation of the original complement of apical filaments. Flattening epidermal cells display randomly oriented microtubules and bundles of thicker filaments (70–100 Å in diameter) which are reminiscent of “tonofibrils” and appear to span the cell from desmosome to desmosome.