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星形胶质细胞上的视网膜神经突生长不会因细胞外基质、抗L1抗体或少突胶质细胞而改变。

Retinal neurite growth on astrocytes is not modified by extracellular matrix, anti-L1 antibody, or oligodendrocytes.

作者信息

Ard M D, Bunge M B, Wood P M, Schachner M, Bunge R P

机构信息

Department of Anatomy, University of Mississippi Medical Center, Jackson 39216.

出版信息

Glia. 1991;4(1):70-82. doi: 10.1002/glia.440040109.

Abstract

Two factors that may influence the course of axonal regeneration in the central nervous system (CNS) are extracellular matrix (ECM) and cell surface molecules that may enhance or inhibit neurite outgrowth. Whereas cultured astrocytes have been reported to be a good substratum for neurite outgrowth, there is recent evidence that cultured oligodendrocytes are inhibitory. To test the influences of 1) ECM components, 2) the L1 adhesion molecule, and 3) the inhibitory potential of mature oligodendrocytes in the astrocytic environment, we have utilized a culture system in which neurites from embryonic rat retina grow vigorously on astrocyte monolayers. The major ECM components were assembled in neonatal rat cortical astrocyte-retina co-cultures only when the medium contained serum. In electron microscopic studies of serum containing cultures, retinal neurites were seen to be related to astrocyte surfaces but rarely were found in contact with ECM; in serum-free medium the association between neurites and astrocytes was similar. In addition, the growth of neurites was vigorous whether ECM was present or absent. Presence of antibodies against the cell surface adhesion molecule L1 did not inhibit retinal neurite elongation on glial fibrillary acidic protein-positive astrocytes. When oligodendrocytes from adult rat spinal cord were combined with the astrocytes, retinal neurites grew as well on the mixed glial population as on astrocytes alone. Immunostaining for galactocerebroside showed many oligodendrocyte processes to be aligned in the direction of neurite growth, suggesting association between the two cell types. This association was verified by electron microscopy. Furthermore, retinal explants extended neurites among myelin basic protein-positive oligodendrocytes cultured without astrocytes. Thus, the astrocyte surface is a strong promoter of neurite growth from embryonic rat retina. This growth did not depend upon either ECM or the L1 adhesion molecule. Because neurites grew on astrocytes in the presence of mature oligodendrocytes or among oligodendrocytes alone, we conclude that oligodendrocytes do not inhibit neurite growth under certain conditions.

摘要

可能影响中枢神经系统(CNS)轴突再生进程的两个因素是细胞外基质(ECM)和可能促进或抑制神经突生长的细胞表面分子。尽管有报道称培养的星形胶质细胞是神经突生长的良好基质,但最近有证据表明培养的少突胶质细胞具有抑制作用。为了测试1)ECM成分、2)L1黏附分子以及3)成熟少突胶质细胞在星形胶质细胞环境中的抑制潜力的影响,我们利用了一种培养系统,其中来自胚胎大鼠视网膜的神经突在星形胶质细胞单层上旺盛生长。仅当培养基中含有血清时,主要的ECM成分才会在新生大鼠皮质星形胶质细胞 - 视网膜共培养物中组装。在对含血清培养物的电子显微镜研究中,可见视网膜神经突与星形胶质细胞表面相关,但很少与ECM接触;在无血清培养基中,神经突与星形胶质细胞之间的关联相似。此外,无论ECM是否存在,神经突的生长都很旺盛。针对细胞表面黏附分子L1的抗体的存在并不抑制视网膜神经突在胶质纤维酸性蛋白阳性星形胶质细胞上的伸长。当将成年大鼠脊髓的少突胶质细胞与星形胶质细胞结合时,视网膜神经突在混合胶质细胞群体上的生长与仅在星形胶质细胞上的生长一样好。半乳糖脑苷脂的免疫染色显示许多少突胶质细胞突起沿神经突生长方向排列,表明两种细胞类型之间存在关联。这种关联通过电子显微镜得到了证实。此外,视网膜外植体在没有星形胶质细胞培养的髓鞘碱性蛋白阳性少突胶质细胞之间延伸神经突。因此,星形胶质细胞表面是胚胎大鼠视网膜神经突生长的有力促进者。这种生长不依赖于ECM或L1黏附分子。因为神经突在成熟少突胶质细胞存在的情况下在星形胶质细胞上生长,或者仅在少突胶质细胞之间生长,所以我们得出结论,在某些条件下少突胶质细胞不会抑制神经突生长。

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