4.8 Article

Understanding the role of tissue-specific decellularized spinal cord matrix hydrogel for neural stem/progenitor cell microenvironment reconstruction and spinal cord injury

期刊

BIOMATERIALS
卷 268, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2020.120596

关键词

Decellularized tissue matrix; Tissue specificity; Spinal cord injury; Neural stem/progenitor cells; Matrisome

资金

  1. National Key R&D Program of China [2016YFC1100103]
  2. National Natural Science Foundation of China [51673220, 52073314, 51903255]
  3. Science and Technology Program of Guangzhou City [201904010364]
  4. Guangdong Innovative and Entrepreneurial Research Team Program [2013S086]
  5. Scientific Instrumentation Development Program of Chinese Academy of Sciences [ZDZBGCH2018005]
  6. Strategic Priority Research Program of Chinese Academy of Sciences [Y84F031]

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The repair of spinal cord injury depends on remodeling the microenvironment and supporting the recruitment and differentiation of endogenous stem/progenitor cells. Decellularized tissue matrices have shown promise in promoting neural tissue regeneration, especially when derived from nervous system tissues. This study compared a DTM hydrogel derived from spinal cord (DSCM-gel) and one derived from peripheral nerves (DNM-gel), with results showing that DSCM-gel promotes NSPC viability, proliferation, migration, and differentiation into neurons in early 3D culturing stages.
The repair of spinal cord injury (SCI) highly relies on microenvironment remodeling and facilitating the recruitment and neuronal differentiation of endogenous stem/progenitor cells. Decellularized tissue matrices (DTMs) have shown their unique and beneficial characteristics in promoting neural tissue regeneration, especially those derived from the nervous system. Herein, we present a comparative analysis of a DTM hydrogel derived from spinal cord (DSCM-gel) and a decellularized matrix hydrogel derived from peripheral nerves (DNM-gel). The tissue-specificity of DSCM-gel was evaluated both in vitro, using neural stem/progenitor cell (NSPC) culture, and in vivo, using various materials and biological analyses, including transcriptome and proteomics. It was found that DSCM-gel retained an extracellular matrix-like nanofibrous structure but exhibited higher porosity than DNM-gel, which potentiated NSPCs viability, proliferation, and migration in the early stage of 3D culturing, followed by facilitation of the NSPCs differentiation into neurons. Transcriptome analysis indicated that DSCM-gel regulates NSPCs behavior by modulating integrin alpha 2, alpha 9, and beta 1 expression profiles along with AKT/ERK related signaling pathways. Proteomics analyses suggest that DSCM specific extracellular matrix proteins, such as the tenascin family (TNC) and some soluble growth factor (FGF2) may contribute to these regulations. Furthermore, in vivo assessments confirmed that DSCM-gel provides a suitable microenvironment for endogenous stem/progenitor cell recruitment and axonal regeneration for bridging the lesion site after a completely transected SCI. Thus, this systematic study provides key insights useful for the development of the tissue-specific DTM biomaterials for translational microenvironment replacement therapies and tissue repair.

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