Canoll P D, Musacchio J M, Hardy R, Reynolds R, Marchionni M A, Salzer J L
Department of Pharmacology, New York University Medical School, New York 10016, USA.
Neuron. 1996 Aug;17(2):229-43. doi: 10.1016/s0896-6273(00)80155-5.
We show that GGF/neuregulin is a mitogen for prooligodendrocytes (O4+/O1- cells), oligodendrocytes (O4+/O1+ cells), and type-2 astrocytes. Heregulin beta 1, another neuregulin isoform, is also mitogenic. The proliferative effect of glial growth factor (GGF) does not require, but is greatly potentiated by, serum factors. GGF also promotes the survival of pro-oligodendrocytes under serum-free conditions. High levels of GGF reversibly inhibit the differentiation and lineage commitment of oligodendrocyte progenitors and, in differentiated cultures, result in loss of O1 and myelin basic protein expression. All three erbB receptors are expressed by progenitors and are activated by GGF; the relative abundance of these receptors changes during differentiation. Finally, cortical neurons release a soluble mitogen for pro-oligodendrocytes that is specifically blocked by antibodies to GGF. These results implicate the neuregulins in the neuronal regulation of oligodendrocyte progenitor proliferation, survival, and differentiation.
我们发现,胶质生长因子/神经调节蛋白是原少突胶质细胞(O4+/O1-细胞)、少突胶质细胞(O4+/O1+细胞)和2型星形胶质细胞的促有丝分裂原。神经调节蛋白β1,另一种神经调节蛋白异构体,也具有促有丝分裂作用。胶质生长因子(GGF)的增殖作用并不依赖血清因子,但血清因子可极大地增强其作用。GGF还能在无血清条件下促进原少突胶质细胞的存活。高水平的GGF可可逆性抑制少突胶质细胞前体细胞的分化和谱系定向,并且在分化培养物中,会导致O1和髓鞘碱性蛋白表达丧失。所有三种erbB受体均由前体细胞表达,并被GGF激活;这些受体的相对丰度在分化过程中会发生变化。最后,皮质神经元释放一种可促进原少突胶质细胞增殖的可溶性有丝分裂原,而该有丝分裂原可被抗GGF抗体特异性阻断。这些结果表明,神经调节蛋白参与了对少突胶质细胞前体细胞增殖、存活及分化的神经元调节。