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白细胞介素-4 凝聚体的延迟给药减轻了星形胶质细胞的神经毒性表型,并促进了挫伤性脊髓损伤后的功能恢复。

Delayed administration of interleukin-4 coacervate alleviates the neurotoxic phenotype of astrocytes and promotes functional recovery after a contusion spinal cord injury.

机构信息

Department of Biomedical Engineering, Rensselaer Polytechnic Institute, 110 8th Street, Troy, NY 12180, United States of America.

Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, 110 8th Street, Troy, NY 12180, United States of America.

出版信息

J Neural Eng. 2024 Aug 14;21(4). doi: 10.1088/1741-2552/ad6596.

Abstract

. Macrophages and astrocytes play a crucial role in the aftermath of a traumatic spinal cord injury (SCI). Infiltrating macrophages adopt a pro-inflammatory phenotype while resident astrocytes adopt a neurotoxic phenotype at the injury site, both of which contribute to neuronal death and inhibit axonal regeneration. The cytokine interleukin-4 (IL-4) has shown significant promise in preclinical models of SCI by alleviating the macrophage-mediated inflammation and promoting functional recovery. However, its effect on neurotoxic reactive astrocytes remains to be elucidated, which we explored in this study. We also studied the beneficial effects of a sustained release of IL-4 from an injectable biomaterial compared to bolus administration of IL-4.. We fabricated a heparin-based coacervate capable of anchoring and releasing bioactive IL-4 and tested its efficacyand. We show that IL-4 coacervate is biocompatible and drives a robust anti-inflammatory macrophage phenotype in culture. We also show that IL-4 and IL-4 coacervate can alleviate the reactive neurotoxic phenotype of astrocytes in culture. Finally, using a murine model of contusion SCI, we show that IL-4 and IL-4 coacervate, injected intraspinally 2 d post-injury, can reduce macrophage-mediated inflammation, and alleviate neurotoxic astrocyte phenotype, acutely and chronically, while also promoting neuroprotection with significant improvements in hindlimb locomotor recovery. We observed that IL-4 coacervate can promote a more robust regenerative macrophage phenotype, as well as match its efficacycompared to bolus IL-4.. Our work shows the promise of coacervate as a great choice for local and prolonged delivery of cytokines like IL-4. We support this by showing that the coacervate can release bioactive IL-4, which acts on macrophages and astrocytes to promote a pro-regenerative environment following a SCI leading to robust neuroprotective and functional outcomes.

摘要

. 巨噬细胞和星形胶质细胞在创伤性脊髓损伤(SCI)后发挥着至关重要的作用。浸润的巨噬细胞表现出促炎表型,而在损伤部位的固有星形胶质细胞表现出神经毒性表型,两者都导致神经元死亡并抑制轴突再生。细胞因子白细胞介素 4(IL-4)在 SCI 的临床前模型中显示出巨大的潜力,通过减轻巨噬细胞介导的炎症并促进功能恢复。然而,其对神经毒性反应性星形胶质细胞的影响仍有待阐明,我们在本研究中对此进行了探讨。我们还研究了从可注射生物材料中持续释放 IL-4 与 IL-4 一次性给药相比的有益效果。. 我们构建了一种基于肝素的凝聚物,能够锚定和释放生物活性的 IL-4,并测试了其疗效。我们表明,IL-4 凝聚物具有生物相容性,并在培养物中驱动强大的抗炎性巨噬细胞表型。我们还表明,IL-4 和 IL-4 凝聚物可以减轻培养物中星形胶质细胞的反应性神经毒性表型。最后,使用挫伤性 SCI 的小鼠模型,我们表明,IL-4 和 IL-4 凝聚物在损伤后 2 天鞘内注射,可以减轻巨噬细胞介导的炎症,并减轻神经毒性星形胶质细胞表型,急性和慢性,同时通过显著改善后肢运动功能恢复来促进神经保护。我们观察到,IL-4 凝聚物可以促进更强大的再生性巨噬细胞表型,并与其疗效相匹配与 IL-4 一次性给药相比。. 我们的工作表明,凝聚物作为局部和长时间输送细胞因子(如 IL-4)的理想选择具有广阔的前景。我们通过显示凝聚物可以释放生物活性的 IL-4,该 IL-4 作用于巨噬细胞和星形胶质细胞,在 SCI 后促进有利于再生的环境,从而产生强大的神经保护和功能结果,为这一观点提供了支持。

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