1 Department of Anatomy and Neurobiology, Virginia Commonwealth University , Richmond, Virginia.
2 Glen Allen High School , Glen Allen, Virginia.
J Neurotrauma. 2018 Jul 15;35(14):1694-1704. doi: 10.1089/neu.2017.5275. Epub 2018 Jun 5.
Traumatic brain injury (TBI) is a prevalent disease with significant costs. Although progress has been made in understanding the complex pathobiology of focal lesions associated with TBI, questions remain regarding the diffuse responses to injury. Expression of the transient receptor potential melastatin 4 (Trpm4) channel is linked to cytotoxic edema during hemorrhagic contusion expansion. However, little is known about Trpm4 following diffuse TBI. To explore Trpm4 expression in diffuse TBI, rats were subjected to a diffuse central fluid percussion injury (CFPI) and survived for 1.5 h to 8 weeks. The total number of Trpm4+ cells, as well as individual cellular intensity/expression of Trpm4, were assessed. Hemotoxylin and eosin (H&E) labeling was performed to evaluate cell damage/death potentially associated with Trpm4 expression following diffuse TBI. Finally, ultrastructural assessments were performed to evaluate the integrity of Trpm4+ cells and the potential for swelling associated with Trpm4 expression. Trpm4 was primarily restricted to astrocytes within the hippocampus and peaked at 6 h post-injury. While the number of Trpm4+ astrocytes returned to sham levels by 8 weeks post-CFPI, cellular intensity occurred in region-specific waves following injury. Correlative H&E assessments demonstrated little evidence of hippocampal damage, suggesting that Trpm4 expression by astrocytes does not precipitate cell death following diffuse TBI. Additionally, ultrastructural assessments showed Trpm4+ astrocytes exhibited twice the soma size compared with Trpm4- astrocytes, indicating that astrocyte swelling is associated with Trpm4 expression. This study provides a foundation for future investigations into the role of Trpm4 in astrocyte swelling and edema following diffuse TBI.
创伤性脑损伤 (TBI) 是一种发病率高、费用高昂的疾病。尽管在理解与 TBI 相关的局灶性病变的复杂病理生物学方面已经取得了进展,但对于损伤后的弥漫性反应仍存在疑问。瞬时受体电位 melastatin 4 (Trpm4) 通道的表达与出血性挫伤扩张过程中的细胞毒性水肿有关。然而,关于弥漫性 TBI 后 Trpm4 的情况知之甚少。为了探讨弥漫性 TBI 中 Trpm4 的表达,对大鼠进行了弥漫性中央液压冲击伤 (CFPI),并在 1.5 h 至 8 周后存活。评估了 Trpm4+细胞的总数以及 Trpm4 的单个细胞强度/表达。进行苏木精和伊红 (H&E) 标记以评估弥漫性 TBI 后与 Trpm4 表达相关的细胞损伤/死亡。最后,进行超微结构评估以评估 Trpm4+细胞的完整性以及与 Trpm4 表达相关的肿胀的可能性。Trpm4 主要局限于海马中的星形胶质细胞,在损伤后 6 小时达到峰值。虽然 CFPI 后 8 周,Trpm4+星形胶质细胞的数量恢复到假手术水平,但细胞强度在损伤后以特定区域的波出现。相关的 H&E 评估表明海马损伤的证据很少,这表明弥漫性 TBI 后星形胶质细胞中 Trpm4 的表达不会引发细胞死亡。此外,超微结构评估显示 Trpm4+星形胶质细胞的体大小是 Trpm4-星形胶质细胞的两倍,表明星形胶质细胞肿胀与 Trpm4 表达有关。这项研究为进一步研究 Trpm4 在弥漫性 TBI 后星形胶质细胞肿胀和水肿中的作用奠定了基础。