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移植的雪旺细胞在脱髓鞘小鼠脊髓中的迁移途径。

Pathways of migration of transplanted Schwann cells in the demyelinated mouse spinal cord.

作者信息

Baron-Van Evercooren A, Duhamel-Clerin E, Boutry J M, Hauw J J, Gumpel M

机构信息

INSERM U134, Hôpital de la Salpêtrière, Paris, France.

出版信息

J Neurosci Res. 1993 Jul 1;35(4):428-38. doi: 10.1002/jnr.490350410.

Abstract

We have studied the behavior of Schwann cells transplanted at a distance from an induced myelin lesion of the adult mouse spinal cord. These transplanted cells were mouse Schwann cells arising from an immortalized cell line (MSC80) which expresses several Schwann cell phenotypes including the ability to produce myelin. The behavior of MSC80 cells was compared to that of purified rat Schwann cells transplanted in the same conditions. Schwann cells were labeled in vitro with the nuclear fluorochrome Hoechst 33342 and were transplanted at distances of 2-8 mm from a lysolecithin-induced myelin lesion in the spinal cord of shiverer and normal mice. Our results show that transplanted MSC80 cells migrated toward the lesion, in both shiverer and normal mouse spinal cord, preferentially along the ependyma, meninges, and blood vessels. They also migrated along white matter tracts but traveled a longer distance in shiverer (8 mm) than in normal (2-3 mm) white matter. Using these different pathways, MSC80 cells arrived within the lesion of shiverer and normal mouse spinal cord at the average speed of 166 microns/hr (8 mm/48 hr). Migration was most efficient along the ependyma and the meninges where it attained up to 250 microns/hr. Migration was much slower in white matter tracts (95 microns/hr +/- 54 in the shiverer and only 38 microns/hr +/- 3 in the normal mouse). We also provide evidence for the specific attraction of MSC80 cells by the lysolecithin-induced lesion since 1) their number increased progressively with time in the lesion, and 2) MSC80 cells left their preferential pathways of migration specifically at the level of the lesion. Finally, combining the Hoechst Schwann cell labeling method with the immunohistochemical detection of the peripheral myelin protein, P0, we show that some of the MSC80 cells which have reached the lesion participate in myelin repair in both shiverer and normal lesioned mouse spinal cord. A series of control experiments performed with rat Schwann cells indicate that the migrating behavior of transplanted MSC80 cells was identical to that of purified but non-immortalized rat Schwann cells.

摘要

我们研究了在成年小鼠脊髓诱导性髓鞘损伤远处移植的施万细胞的行为。这些移植的细胞是源自永生化细胞系(MSC80)的小鼠施万细胞,该细胞系表达多种施万细胞表型,包括产生髓鞘的能力。将MSC80细胞的行为与在相同条件下移植的纯化大鼠施万细胞的行为进行了比较。施万细胞在体外用核荧光染料Hoechst 33342标记,并在距颤抖小鼠和正常小鼠脊髓中溶血卵磷脂诱导的髓鞘损伤2 - 8毫米处进行移植。我们的结果表明,移植的MSC80细胞在颤抖小鼠和正常小鼠脊髓中均向损伤部位迁移,优先沿着室管膜、脑膜和血管迁移。它们也沿着白质束迁移,但在颤抖小鼠白质中迁移的距离(8毫米)比正常小鼠白质中(2 - 3毫米)更长。通过这些不同途径,MSC80细胞以平均166微米/小时(8毫米/48小时)的速度到达颤抖小鼠和正常小鼠脊髓的损伤部位。沿着室管膜和脑膜迁移效率最高,可达250微米/小时。在白质束中迁移要慢得多(颤抖小鼠中为95微米/小时±54,正常小鼠中仅为38微米/小时±3)。我们还提供了证据表明溶血卵磷脂诱导的损伤对MSC80细胞有特异性吸引作用,因为:1)损伤部位的细胞数量随时间逐渐增加;2)MSC80细胞在损伤部位特别离开了它们优先的迁移途径。最后,将Hoechst施万细胞标记方法与外周髓鞘蛋白P0的免疫组织化学检测相结合,我们表明一些到达损伤部位的MSC80细胞参与了颤抖小鼠和正常损伤小鼠脊髓的髓鞘修复。用大鼠施万细胞进行的一系列对照实验表明,移植的MSC80细胞的迁移行为与纯化但未永生化的大鼠施万细胞相同。

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