Connolly J L, Seeley P J, Greene L A
Department of Pathology, Beth Israel Hospital, Boston, MA.
Neurochem Res. 1987 Oct;12(10):861-8. doi: 10.1007/BF00966307.
Scanning electron microscopy was used to study regulation of growth cone shape and surface morphology by nerve growth factor (NGF). The growth cones of cultured rat sympathetic neurons and neuronally-differentiated PC12 cells were observed under conditions of continuous NGF exposure, NGF withdrawal, and NGF readdition. Growth cones of cells cultured in the continuous presence of NGF were mostly spread in shape and about 60% possessed surface ruffles. Ruffles appeared to be largely restricted to growth cones in that few were observed on cell bodies and neurites. Withdrawal of NGF for 4-5 hr caused most of the growth cones to take on a non-spread or contracted appearance and to lose their ruffles. Readdition of NGF promoted rapid changes in growth cone properties. Within 30 sec, ruffling was again evident on the growth cones and remained prominent there throughout the course of treatment (up to 5 hr). This was in contrast to cell bodies on which, as previously reported, ruffling also occurred following NGF readdition, but only transiently (for less than 15 min). Respreading of growth cones also occurred under these conditions. This was evident within 1 min of NGF readdition and reached the levels observed in continuously-treated cultures within 1-2 hr. Neurites were also examined. Ruffles were only rarely present in the continuous presence of NGF and were absent after NGF withdrawal. NGF readdition elicited ruffling along neurites within 30 sec; the prevalence of such ruffles diminished to that seen in continuously-treated cultures within about an hour.(ABSTRACT TRUNCATED AT 250 WORDS)
利用扫描电子显微镜研究神经生长因子(NGF)对生长锥形状和表面形态的调节作用。在持续暴露于NGF、撤除NGF以及重新添加NGF的条件下,观察培养的大鼠交感神经元和神经分化的PC12细胞的生长锥。持续存在NGF培养的细胞的生长锥大多呈展开状,约60%具有表面褶皱。褶皱似乎主要局限于生长锥,在细胞体和神经突上很少观察到。撤除NGF 4 - 5小时导致大多数生长锥呈现非展开或收缩的外观,并失去其褶皱。重新添加NGF促进了生长锥特性的快速变化。在30秒内,生长锥上再次明显出现褶皱,并且在整个处理过程中(长达5小时)一直很突出。这与细胞体形成对比,如先前报道,重新添加NGF后细胞体上也会出现褶皱,但只是短暂出现(少于15分钟)。在这些条件下生长锥也会重新展开。这在重新添加NGF后1分钟内就很明显,并在1 - 2小时内达到持续处理培养物中观察到的水平。还对神经突进行了检查。在持续存在NGF的情况下很少出现褶皱,撤除NGF后则不存在。重新添加NGF在30秒内会引起神经突出现褶皱;大约1小时内,这种褶皱的发生率降至持续处理培养物中的水平。(摘要截短于250字)