RETINAL GANGLION-CELLS LOSE RESPONSE TO LAMININ WITH MATURATION
RETINAL GANGLION-CELLS LOSE RESPONSE TO LAMININ WITH MATURATION
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DOI:
10.1038/322465a0
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发表时间:
1986-07-31
期刊:
影响因子:
64.8
通讯作者:
BARTLETT, P
中科院分区:
文献类型:
--
作者:
COHEN, J;BURNE, JF;BARTLETT, P
The decisive role played by adhesive interactions between neuronal processes and the culture substrate in determining the form and extent of neurite outgrowthin vitro1,2has greatly influenced ideas about the mechanisms of axonal growth and guidance in the vertebrate nervous system. These studies have also helped to identify adhesive molecules that might be involved in guiding axonal growthin vivo. One candidate molecule is laminin, a major gly-coprotein of basal laminae3which has been shown to induce a wide variety of embryonic neurones to extend neurites in culture4–8. Moreover, laminin is found in large amounts in injured nerves that can successfully regenerate but is absent from nerves where regeneration fails9–11. However, it is unclear to what extent the mechanisms that regulate axonal regeneration also operate in the embryo when axon outgrowth is initiated. Here we have examined the substrate requirements for neurite outgrowthin vitroby chick embryo retinal ganglion cells, the only cells in the retina to send axons to the brain. We show that while retinal ganglion cells from embryonic day 6 (E6) chicks extend profuse neurites on laminin, those from Ell do not, although they retain the ability to extend neurites on astrocytes via a laminin-independent mechanism. This represents the first evidence that central nervous system neurones may undergo a change in their substrate requirements for neurite outgrowth as they mature.