Yoon Hyesook, Walters Grant, Paulsen Alex R, Scarisbrick Isobel A
Department of Physical Medicine and Rehabilitation, Rehabilitation Medicine Research Center, Mayo Clinic, Rochester, Minnesota, United States of America.
Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One. 2017 Jul 10;12(7):e0180697. doi: 10.1371/journal.pone.0180697. eCollection 2017.
Astrocytes have emerged as essential regulators of function and response to injury in the brain and spinal cord, yet very little is known about regional differences that exist. Here we compare the expression of key astroglial markers (glial fibrillary acidic protein (GFAP) and Aldehyde Dehydrogenase-1 Family Member L1 (ALDH1L1)) across these disparate poles of the neuraxis, tracking their expression developmentally and in the context of demyelination. In addition, we document changes in the astrocyte regulatory cytokine interleukin 6 (IL-6), and its signaling partner signal transducer and activator of transcription 3 (STAT3), in vivo and in vitro. Results demonstrate that GFAP expression is higher in the developing and adult spinal cord relative to brain. Comparisons between GFAP and ALDH1L1 expression suggest elevations in spinal cord GFAP during the early postnatal period reflect an accelerated appearance of astrocytes, while elevations in adulthood reflect higher expression by individual astrocytes. Notably, increases in spinal cord compared to whole brain GFAP were paralleled by higher levels of IL-6 and STAT3. Equivalent elevations in GFAP, GFAP/ALDH1L1 ratios, and in IL-6, were observed in primary astrocyte cultures derived from spinal cord compared to cortex. Also, higher levels of GFAP were observed in the spinal cord compared to the brain after focal demyelinating injury. Altogether, these studies point to key differences in astrocyte abundance and the expression of GFAP and IL-6 across the brain and spinal cord that are positioned to influence regional specialization developmentally and responses occurring in the context of injury and disease.
星形胶质细胞已成为大脑和脊髓功能及损伤反应的重要调节因子,但对于存在的区域差异却知之甚少。在此,我们比较了关键星形胶质细胞标志物(胶质纤维酸性蛋白(GFAP)和醛脱氢酶1家族成员L1(ALDH1L1))在神经轴这两个不同部位的表达情况,追踪它们在发育过程中和脱髓鞘情况下的表达。此外,我们记录了星形胶质细胞调节细胞因子白细胞介素6(IL-6)及其信号转导伴侣信号转导和转录激活因子3(STAT3)在体内和体外的变化。结果表明,相对于大脑,GFAP在发育中的和成年脊髓中的表达更高。GFAP和ALDH1L1表达之间的比较表明,出生后早期脊髓GFAP的升高反映了星形胶质细胞的加速出现,而成年期的升高反映了单个星形胶质细胞的更高表达。值得注意的是,与全脑相比,脊髓GFAP的增加与IL-6和STAT3的更高水平平行。与皮质相比,在源自脊髓的原代星形胶质细胞培养物中观察到GFAP、GFAP/ALDH1L1比值以及IL-6的同等升高。此外,局灶性脱髓鞘损伤后,与大脑相比,脊髓中观察到更高水平的GFAP。总之,这些研究指出了星形胶质细胞丰度以及GFAP和IL-6在大脑和脊髓中的表达存在关键差异,这些差异可能在发育过程中影响区域特化以及在损伤和疾病情况下发生的反应。