Mayer Joshua A, Figari Carlos, Radcliff Abigail B, Mckee Camille, Duncan Ian D
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, 53706.
J Comp Neurol. 2016 Apr 1;524(5):930-9. doi: 10.1002/cne.23882. Epub 2015 Sep 4.
We studied the developmental pattern of oligodendrocyte differentiation and myelin formation in the fetal canine spinal cord from E40 to P0. The pattern of development matches what has been described in the spinal cord of humans, rodents, and many other species. Oligodendrocytes were first found at E40, close to the central canal, with their spread in a tangential manner to the ventral and then lateral columns. Myelin development followed the same pattern but was not seen until E46. A clear subpial zone lacking glial cells and myelin was seen in the lateral column in early development, suggesting that there may also be a radial component of migration of oligodendrocyte progenitor cells (OPCs) from a ventral site. This spatial-temporal developmental pattern seen in wild type matches a delay in myelination of the superficial tracts of the spinal cord seen in a canine myelin mutant, suggesting that the mutation prevents the distribution and differentiation of OPCs at an early, but narrow, window of time during fetal development.
我们研究了胎犬脊髓中少突胶质细胞分化和髓鞘形成从胚胎第40天(E40)到出生后第0天(P0)的发育模式。这种发育模式与人类、啮齿动物和许多其他物种脊髓中所描述的一致。少突胶质细胞最早在E40时于靠近中央管处被发现,随后以切线方式向腹侧柱和外侧柱扩散。髓鞘发育遵循相同模式,但直到E46才可见。在发育早期,外侧柱中可见一个明显缺乏胶质细胞和髓鞘的软膜下区域,这表明少突胶质细胞前体细胞(OPCs)可能也存在从腹侧位点进行放射状迁移的成分。在野生型中观察到的这种时空发育模式与犬髓鞘突变体中脊髓浅表束髓鞘形成延迟相匹配,这表明该突变在胎儿发育的早期但狭窄的时间段内阻止了OPCs的分布和分化。