Prince of Wales Medical Research Institute, Sydney, New South Wales, Australia
J Neurosurg Spine. 2011 May;14(5):573-82. doi: 10.3171/2011.1.SPINE09491. Epub 2011 Feb 25.
Endogenous stem cells theoretically could replace lost tissue and repair deficits caused by syringes. In this study the authors quantitatively examined 1) whether neural progenitor cells exist in an adult rat model of posttraumatic syringomyelia (PTS); 2) and if so, how long an active population of progenitor cells can persist; 3) whether the cell population's location is associated with the syrinx; 4) the degree of differentiation of the progenitor cells; and 5) the phenotypic fate of the progenitor cells.
Wistar rats were divided into intact, sham-operated, and experimental syrinx groups. Animals in each group were equally subdivided according to 4 time points: 7, 14, 28, and 56 days post-syrinx induction. Rats in the experimental syrinx group underwent a C-7 and T-1 laminectomy and then received 0.5 μl of a 24-mg/ml quisqualic acid spinal cord injection at the C-8 level to mimic an excitotoxic injury with an initial cyst, and 10 μl of a 250-mg/ml kaolin injection into the subarachnoid space at the C-8 level to create arachnoiditis. The proliferation, distribution, and differentiation of endogenous progenitor cells were identified immunocytochemically.
The authors observed a 20-fold increase in progenitor cells excluding inflammatory cells in the 1st 2 weeks post-syrinx induction. The cells persisted for at least 56 days, and 80% of them were located in the gray matter along the border of cysts. They included neural multipotential progenitor cells, oligodendroglial progenitor cells, and astrocytes.
Data in this study provide evidence for proliferation, distribution, and differentiation of endogenous progenitor cells in a model of PTS in adult rats. These progenitor cells proliferate rapidly, extend for long periods, and are mainly located in the gray matter along the border of syringes. Neural multipotential progenitor cells are expected to be associated with reparative and regenerative mechanisms of PTS. Glial cells are involved in the formation of a glial scar barrier that surrounds the syrinx and may prevent cyst enlargement. The authors' findings suggest that neural progenitor cells play a protective role in PTS.
理论上,内源性干细胞可以替代因脊髓空洞症而丢失的组织并修复由此导致的缺陷。本研究定量检测了 1)在创伤性脊髓空洞症(PTS)的成年大鼠模型中是否存在神经祖细胞;2)如果存在,祖细胞的活跃群体可以持续多长时间;3)细胞群体的位置是否与脊髓空洞症有关;4)祖细胞的分化程度;以及 5)祖细胞的表型命运。
Wistar 大鼠分为完整、假手术和实验性脊髓空洞症组。每组动物根据 4 个时间点分为相等的亚组:脊髓空洞症诱导后 7、14、28 和 56 天。实验组大鼠行 C-7 和 T-1 椎板切除术,然后在 C-8 水平接受 0.5 μl 浓度为 24mg/ml 的海人藻酸脊髓内注射,以模拟兴奋性损伤,形成初始囊肿,并在 C-8 水平蛛网膜下腔注射 10 μl 浓度为 250mg/ml 的高岭土,形成蛛网膜炎。通过免疫细胞化学鉴定内源性祖细胞的增殖、分布和分化。
作者观察到,在脊髓空洞症诱导后 2 周内,祖细胞的数量增加了 20 倍,排除了炎症细胞。这些细胞至少持续存在 56 天,其中 80%位于囊肿边缘的灰质中。它们包括神经多潜能祖细胞、少突胶质祖细胞和星形胶质细胞。
本研究的数据为成年大鼠 PTS 模型中内源性祖细胞的增殖、分布和分化提供了证据。这些祖细胞增殖迅速,持续时间长,主要位于脊髓空洞症边缘的灰质中。神经多潜能祖细胞可能与 PTS 的修复和再生机制有关。神经胶质细胞参与形成围绕脊髓空洞症的胶质瘢痕屏障,可能阻止囊肿扩大。作者的研究结果表明,神经祖细胞在 PTS 中起保护作用。