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星形胶质细胞起源于神经干细胞,驱动脊髓损伤病理性 CSPGs 的再生重塑。

Astrocytes originated from neural stem cells drive the regenerative remodeling of pathologic CSPGs in spinal cord injury.

机构信息

Department of Physiology and Pathophysiology, Spinal Cord Research Centre, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada; Manitoba Multiple Sclerosis Research Center, Winnipeg, MB, Canada.

Department of Physiology and Pathophysiology, Spinal Cord Research Centre, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada; Manitoba Multiple Sclerosis Research Center, Winnipeg, MB, Canada; Children Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.

出版信息

Stem Cell Reports. 2024 Oct 8;19(10):1451-1473. doi: 10.1016/j.stemcr.2024.08.007. Epub 2024 Sep 19.

Abstract

Neural degeneration is a hallmark of spinal cord injury (SCI). Multipotent neural precursor cells (NPCs) have the potential to reconstruct the damaged neuron-glia network due to their tri-lineage capacity to generate neurons, astrocytes, and oligodendrocytes. However, astrogenesis is the predominant fate of resident or transplanted NPCs in the SCI milieu adding to the abundant number of resident astrocytes in the lesion. How NPC-derived astrocytes respond to the inflammatory milieu of SCI and the mechanisms by which they contribute to the post-injury recovery processes remain largely unknown. Here, we uncover that activated NPC-derived astrocytes exhibit distinct molecular signature that is immune modulatory and foster neurogenesis, neuronal maturity, and synaptogenesis. Mechanistically, NPC-derived astrocytes perform regenerative matrix remodeling by clearing inhibitory chondroitin sulfate proteoglycans (CSPGs) from the injury milieu through LAR and PTP-σ receptor-mediated endocytosis and the production of ADAMTS1 and ADAMTS9, while most resident astrocytes are pro-inflammatory and contribute to the pathologic deposition of CSPGs. These novel findings unravel critical mechanisms of NPC-mediated astrogenesis in SCI repair.

摘要

神经退行性变是脊髓损伤 (SCI) 的标志。多能神经前体细胞 (NPCs) 具有重建损伤神经元-神经胶质网络的潜力,因为它们具有产生神经元、星形胶质细胞和少突胶质细胞的三系能力。然而,在 SCI 环境中,内源性或移植的 NPC 向星形胶质细胞分化是主要命运,这增加了病变中大量内源性星形胶质细胞的数量。NPC 衍生的星形胶质细胞如何响应 SCI 的炎症微环境,以及它们如何促进损伤后恢复过程仍知之甚少。在这里,我们揭示了活化的 NPC 衍生的星形胶质细胞表现出独特的分子特征,具有免疫调节作用,并促进神经发生、神经元成熟和突触形成。从机制上讲,NPC 衍生的星形胶质细胞通过 LAR 和 PTP-σ 受体介导的内吞作用以及 ADAMTS1 和 ADAMTS9 的产生,从损伤微环境中清除抑制性软骨素硫酸盐蛋白聚糖 (CSPGs),从而进行再生基质重塑,而大多数内源性星形胶质细胞具有促炎作用,并有助于 CSPGs 的病理性沉积。这些新发现揭示了 NPC 介导的 SCI 修复中星形胶质细胞发生的关键机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96e8/11561464/13ef960f5eec/fx1.jpg

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