Nano-scaffold containing functional motif of stromal cell-derived factor 1 enhances neural stem cell behavior and synaptogenesis in traumatic brain injury

Sci Rep. 2025 Feb 17;15(1):5811. doi: 10.1038/s41598-025-85698-5.

Abstract

Traumatic brain injury (TBI) is a leading cause of mortality and morbidity worldwide, presenting a significant challenge due to the lack of effective therapies. Neural stem cells (NSCs) have shown promising potential in preclinical studies as a therapy for TBI. However, their application is limited by challenges related to poor survival and integration within the injured brain. This study investigated the effect of a novel nano-scaffold containing stromal cell-derived factor 1 (SDF-1) on NSC behavior and synaptogenesis after TBI. Using an innovative design, we successfully fabricated a nano-scaffold with Young's modulus of approximately 3.21 kPa, which aligns closely with the mechanical properties exhibited by neural tissue. This achievement marks the first time such a scaffold has been created and has promising implications for its potential use in neural tissue engineering applications. Our findings demonstrate that the nano-scaffold enhances NSC proliferation, migration, and differentiation capacity in vitro. Moreover, when transplanted into the injured brain, the nano-scaffold promotes the survival and integration of NSCs, leading to increased synaptogenesis and functional recovery. These findings suggest that using the novel nano-scaffold containing SDF-1 could provide a promising approach to treating TBI by improving NSC behavior and promoting synaptogenesis.

Keywords: Brain injury; CXCL12; Nano-scaffold; Synaptic transmission; Tissue engineering.

MeSH terms

  • Animals
  • Brain Injuries, Traumatic* / metabolism
  • Brain Injuries, Traumatic* / pathology
  • Brain Injuries, Traumatic* / therapy
  • Cell Differentiation / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Chemokine CXCL12* / chemistry
  • Chemokine CXCL12* / metabolism
  • Chemokine CXCL12* / pharmacology
  • Male
  • Mice
  • Neural Stem Cells* / cytology
  • Neural Stem Cells* / drug effects
  • Neural Stem Cells* / metabolism
  • Neurogenesis* / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Synapses* / metabolism
  • Synapses* / physiology
  • Tissue Engineering / methods
  • Tissue Scaffolds* / chemistry

Substances

  • Chemokine CXCL12