Urinary bladder extracellular matrix hydrogels and matrix-bound vesicles differentially regulate central nervous system neuron viability and axon growth and branching

被引:35
作者
Faust, Anne [1 ,2 ]
Kandakatla, Apoorva [1 ,2 ]
van der Merwe, Yolandi [1 ,2 ,3 ]
Ren, Tanchen [1 ,2 ]
Huleihel, Luai [2 ,4 ]
Hussey, George [2 ,4 ]
Naranjo, Juan Diego [2 ,4 ]
Johnson, Scott [2 ,4 ]
Badylak, Stephen [2 ,4 ]
Steketee, Michael [1 ,2 ,5 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Ophthalmol, Pittsburgh, PA 15261 USA
[2] McGowan Inst Regenerat Med, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Bioengn, Swanson Sch Engn, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Dept Surg, Pittsburgh, PA USA
[5] Univ Pittsburgh, Ctr Neurosci, Pittsburgh, PA 15260 USA
关键词
Extracellular matrix; matrix bound vesicles; neuroprotection; axon growth; hippocampal neuron; microglia; RETINAL GANGLION-CELLS; BIOLOGIC SCAFFOLD; MACROPHAGE PHENOTYPE; CONE MOTILITY; ECM HYDROGEL; MOUSE MODEL; TISSUE; REGENERATION; GUIDANCE; CNS;
D O I
10.1177/0885328217698062
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:1277 / 1295
页数:19
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