Faust Anne, Kandakatla Apoorva, van der Merwe Yolandi, Ren Tanchen, Huleihel Luai, Hussey George, Naranjo Juan Diego, Johnson Scott, Badylak Stephen, Steketee Michael
1 Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
2 McGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA.
J Biomater Appl. 2017 Apr;31(9):1277-1295. doi: 10.1177/0885328217698062. Epub 2017 Mar 9.
Central nervous system neurons often degenerate after trauma due to the inflammatory innate immune response to injury, which can lead to neuronal cell death, scarring, and permanently lost neurologic function. Extracellular matrix bioscaffolds, derived by decellularizing healthy tissues, have been widely used in both preclinical and clinical studies to promote positive tissue remodeling, including neurogenesis, in numerous tissues, with extracellular matrix from homologous tissues often inducing more positive responses. Extracellular matrix hydrogels are liquid at room temperature and enable minimally invasive extracellular matrix injections into central nervous system tissues, before gelation at 37℃. However, few studies have analyzed how extracellular matrix hydrogels influence primary central nervous system neuron survival and growth, and whether central nervous system and non-central nervous system extracellular matrix specificity is critical to neuronal responses. Urinary bladder extracellular matrix hydrogels increase both primary hippocampal neuron survival and neurite growth to similar or even greater extents, suggesting extracellular matrix from non-homologous tissue sources, such as urinary bladder matrix-extracellular matrix, may be a more economical and safer alternative to developing central nervous system extracellular matrices for central nervous system applications. Additionally, we show matrix-bound vesicles derived from urinary bladder extracellular matrix are endocytosed by hippocampal neurons and positively regulate primary hippocampal neuron neurite growth. Matrix-bound vesicles carry protein and RNA cargos, including noncoding RNAs and miRNAs that map to the human genome and are known to regulate cellular processes. Thus, urinary bladder matrix-bound vesicles provide natural and transfectable cargoes which offer new experimental tools and therapeutic applications to study and treat central nervous system neuron injury.
中枢神经系统神经元在创伤后常因对损伤的炎症性先天免疫反应而退化,这可能导致神经元细胞死亡、瘢痕形成和永久性神经功能丧失。通过对健康组织进行脱细胞处理得到的细胞外基质生物支架,已广泛应用于临床前和临床研究,以促进包括神经发生在内的多种组织中的积极组织重塑,同源组织的细胞外基质通常会诱导更积极的反应。细胞外基质水凝胶在室温下呈液态,能够在37℃凝胶化之前将其微创注射到中枢神经系统组织中。然而,很少有研究分析细胞外基质水凝胶如何影响原代中枢神经系统神经元的存活和生长,以及中枢神经系统和非中枢神经系统细胞外基质的特异性对神经元反应是否至关重要。膀胱细胞外基质水凝胶在相似甚至更大程度上增加了原代海马神经元的存活和神经突生长,这表明来自非同源组织来源的细胞外基质,如膀胱基质细胞外基质,可能是开发用于中枢神经系统应用的中枢神经系统细胞外基质的一种更经济、更安全的替代方案。此外,我们发现源自膀胱细胞外基质的基质结合囊泡被海马神经元内吞,并正向调节原代海马神经元的神经突生长。基质结合囊泡携带蛋白质和RNA货物,包括与人类基因组图谱相关的非编码RNA和miRNA,已知它们可调节细胞过程。因此,膀胱基质结合囊泡提供了天然且可转染的货物,为研究和治疗中枢神经系统神经元损伤提供了新的实验工具和治疗应用。