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少突胶质细胞的存活是否依赖于轴突?

Does oligodendrocyte survival depend on axons?

作者信息

Barres B A, Jacobson M D, Schmid R, Sendtner M, Raff M C

机构信息

Medical Research Council Developmental Neurobiology Programme, Department of Biology, Medawar Building, University College, London WC1E 6BT, UK.

出版信息

Curr Biol. 1993 Aug 1;3(8):489-97. doi: 10.1016/0960-9822(93)90039-q.

Abstract

BACKGROUND

We have shown previously that oligodendrocytes and their precursors require signals from other cells in order to survive in culture. In addition, we have shown that about 50% of the oligodendrocytes produced in the developing rat optic nerve normally die, apparently in a competition for the limiting amounts of survival factors. We have hypothesized that axons may control the levels of such oligodendrocyte survival factors and that the competition-dependent death of oligodendrocytes serves to match their numbers to the number of axons that they myelinate. Here we test one prediction of this hypothesis - that the survival of developing oligodendrocytes depends on axons.

RESULTS

We show that oligodendrocyte death occurs selectively in transected nerves in which the axons degenerate. This cell death is prevented by the delivery of exogenous ciliary neurotrophic factor (CNTF) or insulin-like growth factor I (IGF-1), both of which have been shown to promote oligodendrocyte survival in vitro. We also show that purified neurons promote the survival of purified oligodendrocytes in vitro.

CONCLUSION

These results strongly suggest that oligodendrocyte survival depends upon the presence of axons; they also support the hypothesis that a competition for axon-dependent survival signals normally helps adjust the number of oligodendrocytes to the number of axons that require myelination. The identities of these signals remain to be determined.

摘要

背景

我们之前已经表明,少突胶质细胞及其前体细胞在培养中存活需要来自其他细胞的信号。此外,我们还表明,发育中的大鼠视神经中产生的约50%的少突胶质细胞通常会死亡,显然是在竞争有限量的存活因子。我们推测轴突可能控制此类少突胶质细胞存活因子的水平,并且少突胶质细胞依赖竞争的死亡有助于使其数量与它们髓鞘化的轴突数量相匹配。在此,我们检验这一假说的一个预测——发育中的少突胶质细胞的存活取决于轴突。

结果

我们发现少突胶质细胞死亡选择性地发生在轴突退化的横断神经中。这种细胞死亡可通过外源性睫状神经营养因子(CNTF)或胰岛素样生长因子I(IGF-1)的递送而被阻止,这两种因子在体外均已被证明可促进少突胶质细胞存活。我们还表明,纯化的神经元在体外可促进纯化的少突胶质细胞存活。

结论

这些结果有力地表明少突胶质细胞的存活取决于轴突的存在;它们也支持这样的假说,即对轴突依赖性存活信号的竞争通常有助于将少突胶质细胞的数量调整到需要髓鞘化的轴突数量。这些信号的身份仍有待确定。

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