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Developmental changes in myelin-induced proliferation of cultured Schwann cells.培养的施万细胞中髓鞘诱导增殖的发育变化。
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2
Differential proliferative responses of cultured Schwann cells to axolemma- and myelin-enriched fractions. I. Biochemical studies.培养的雪旺细胞对富含轴膜和髓磷脂组分的不同增殖反应。I. 生化研究。
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Differential proliferative responses of cultured Schwann cells to axolemma and myelin-enriched fractions. II. Morphological studies.培养的雪旺细胞对轴膜和富含髓磷脂组分的不同增殖反应。II. 形态学研究。
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引用本文的文献

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Satellite cell proliferation in the adult rat trigeminal ganglion results from the release of a mitogenic protein from explanted sensory neurons.成年大鼠三叉神经节中的卫星细胞增殖源于外植感觉神经元释放的一种促有丝分裂蛋白。
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本文引用的文献

1
Myelin-specific proteins and glycolipids in rat Schwann cells and oligodendrocytes in culture.培养的大鼠雪旺细胞和少突胶质细胞中的髓鞘特异性蛋白质和糖脂。
J Cell Biol. 1980 Mar;84(3):483-94. doi: 10.1083/jcb.84.3.483.
2
Mitogenicity of brain axolemma membranes and soluble factors for dorsal root ganglion Schwann cells.脑轴突膜和可溶性因子对背根神经节雪旺细胞的促有丝分裂活性
J Cell Biochem. 1982;18(4):433-45. doi: 10.1002/jcb.1982.240180405.
3
Axolemma-enriched fractions isolated from PNS and CNS are mitogenic for cultured Schwann cells.从周围神经系统(PNS)和中枢神经系统(CNS)分离出的富含轴突膜的组分对培养的雪旺细胞具有促有丝分裂作用。
Brain Res. 1982 Feb;255(2):295-9. doi: 10.1016/0165-3806(82)90028-1.
4
Further studies on the mitogenic response of cultured Schwann cells to rat CNS axolemma-enriched fractions.对培养的雪旺细胞对富含大鼠中枢神经系统轴膜成分的有丝分裂原反应的进一步研究。
Brain Res. 1983 Jul;285(1):87-93. doi: 10.1016/0165-3806(83)90112-8.
5
The role of non-resident cells in Wallerian degeneration.非驻留细胞在沃勒变性中的作用。
J Neurocytol. 1984 Oct;13(5):767-96. doi: 10.1007/BF01148493.
6
Differential proliferative responses of cultured Schwann cells to axolemma- and myelin-enriched fractions. I. Biochemical studies.培养的雪旺细胞对富含轴膜和髓磷脂组分的不同增殖反应。I. 生化研究。
J Cell Biol. 1984 Dec;99(6):2309-13. doi: 10.1083/jcb.99.6.2309.
7
Studies of Schwann cell proliferation. I. An analysis in tissue culture of proliferation during development, Wallerian degeneration, and direct injury.施万细胞增殖的研究。I. 发育、华勒氏变性和直接损伤过程中增殖的组织培养分析。
J Cell Biol. 1980 Mar;84(3):739-52. doi: 10.1083/jcb.84.3.739.
8
Enzyme-labeled antibodies for the light and electron microscopic localization of tissue antigens.用于组织抗原光镜和电镜定位的酶标抗体。
J Cell Biol. 1967 May;33(2):307-18. doi: 10.1083/jcb.33.2.307.
9
Duration of synthesis phase in neuilemma cells in mouse sciatic nerve during degeneration.小鼠坐骨神经变性过程中神经膜细胞合成期的持续时间。
Exp Neurol. 1970 Feb;26(2):275-82. doi: 10.1016/0014-4886(70)90125-1.
10
Differential proliferative responses of cultured Schwann cells to axolemma and myelin-enriched fractions. II. Morphological studies.培养的雪旺细胞对轴膜和富含髓磷脂组分的不同增殖反应。II. 形态学研究。
J Neurocytol. 1985 Aug;14(4):619-35. doi: 10.1007/BF01200801.

培养的施万细胞中髓鞘诱导增殖的发育变化。

Developmental changes in myelin-induced proliferation of cultured Schwann cells.

作者信息

Yoshino J E, Mason P W, DeVries G H

出版信息

J Cell Biol. 1987 Mar;104(3):655-60. doi: 10.1083/jcb.104.3.655.

DOI:10.1083/jcb.104.3.655
PMID:2434514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2114551/
Abstract

Schwann cell proliferation induced by a myelin-enriched fraction was examined in vitro. Although nearly all the Schwann cells contained material that was recognized by antisera to myelin basic protein after 24 h, only 1% of the cells were synthesizing DNA. 72 h after the addition of the mitogen a maximum of 10% of the cells incorporated [3H]thymidine. If the cultures were treated with the myelin-enriched fraction for 24 h and then washed, the number of proliferating Schwann cells decreased by 75% when compared with those cells that were incubated with the mitogen continuously. When Schwann cells were labeled with [14C]thymidine followed by a pulse of [3H]thymidine 24 h later, every Schwann cell labeled with [3H]thymidine was also labeled with [14C]thymidine. Although almost every Schwann cell can metabolize the myelin membranes within 24 h of exposure, a small population of cell initially utilizes the myelin as a mitogen, and this population continues to divide only if myelin is present in the extracellular media. The percentage of the Schwann cells that initially recognize the myelin-enriched fraction as a mitogen is dependent upon the age of the animal from which the cells were prepared.

摘要

在体外检测了富含髓磷脂的组分诱导的雪旺细胞增殖。虽然几乎所有雪旺细胞在24小时后都含有能被抗髓磷脂碱性蛋白抗血清识别的物质,但只有1%的细胞在合成DNA。加入促有丝分裂原72小时后,最多10%的细胞掺入了[3H]胸腺嘧啶核苷。如果培养物用富含髓磷脂的组分处理24小时,然后洗涤,与持续用促有丝分裂原孵育的细胞相比,增殖的雪旺细胞数量减少了75%。当雪旺细胞先用[14C]胸腺嘧啶核苷标记,24小时后再用[3H]胸腺嘧啶核苷脉冲标记时,每个用[3H]胸腺嘧啶核苷标记的雪旺细胞也都被[14C]胸腺嘧啶核苷标记。虽然几乎每个雪旺细胞在接触后24小时内都能代谢髓磷脂膜,但一小部分细胞最初将髓磷脂用作促有丝分裂原,并且只有当细胞外培养基中存在髓磷脂时,这部分细胞才会继续分裂。最初将富含髓磷脂的组分识别为促有丝分裂原的雪旺细胞百分比取决于制备细胞的动物的年龄。