TGFβ3 is neuroprotective and alleviates the neurotoxic response induced by aligned poly-l-lactic acid fibers on naïve and activated primary astrocytes. (November 2020)

• Record Type: Journal Article
• Authors: Gottipati, Manoj K.; D'Amato, Anthony R.; Ziemba, Alexis M.; Popovich, Phillip G.; Gilbert, Ryan J.
• Is Part Of: Acta biomaterialia. Volume 117(2020)
• Page Start: 273
• Page End: 282
• Publication Date: 2020-11
• Subjects: Astrocytes -- Reactivity -- Macrophage conditioned media -- Transforming growth factor β3 -- Spinal cord injury; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1016/j.actbio.2020.09.057
• Languages: English
• ISSNs: 1742-7061

Abstract

Abstract: Following spinal cord injury, astrocytes at the site of injury become reactive and exhibit a neurotoxic (A1) phenotype, which leads to neuronal death. In addition, the glial scar, which is composed of reactive astrocytes, acts as a chemical and physical barrier to subsequent axonal regeneration. Biomaterials, specifically electrospun fibers, induce a migratory phenotype of astrocytes and promote regeneration of axons following acute spinal cord injury in preclinical models. However, no study has examined the potential of electrospun fibers or biomaterials in general to modulate neurotoxic (A1) or neuroprotective (A2) astrocytic phenotypes. To assess astrocyte reactivity in response to aligned poly-l -lactic acid microfibers, naïve spinal cord astrocytes or spinal cord astrocytes primed towards the neurotoxic phenotype (A1) were cultured on fibrous scaffolds. Gene expression analysis of the pan-reactive astrocyte makers (GFAP, Lcn2, SerpinA3), A1 specific markers (H2-D1, SerpinG1), and A2 specific makers (Emp1, S100a10) was done using quantitative polymerase chain reaction (qPCR). Electrospun fibers mildly increased the expression of the pan-reactive and A1-specific markers, showing the ability of fibrous materials to induce a more reactive, A1 phenotype. However, when naïve or activated astrocytes were cultured on fibers in the presence of transforming growth factor β3 (TGFβ3), the expression of A1-specific markers was greatly reduced, which in turn improved neuronal survival in culture. Graphical abstract: Image, graphical abstract