# 3D printed collagen/silk fibroin scaffolds carrying the secretome of human umbilical mesenchymal stem cells ameliorated neurological dysfunction after spinal cord injury in rats

**Authors:** Chong Chen, Hai-Huan Xu, Xiao-Yin Liu, Yu-Sheng Zhang, Lin Zhong, You-Wei Wang, Lin Xu, Pan Wei, Ya-Xing Chen, Peng Liu, Chen-Ru Hao, Xiao-Li Jia, Nan Hu, Xiao-Yang Wu, Xiao-Song Gu, Li-Qun Chen, Xiao-Hong Li

PMC · DOI: 10.1093/rb/rbac014 · 2022-02-24

## TL;DR

3D printed scaffolds with stem cell secretome improved spinal cord injury recovery in rats by aiding nerve regeneration and function.

## Contribution

3D printed collagen/silk fibroin scaffolds with MSC secretome enhance SCI recovery more effectively than scaffolds alone.

## Key findings

- MSC secretome-containing scaffolds improved hindlimb locomotor function in rats.
- The secretome facilitated nerve fiber regeneration and remyelination at the injury site.
- Synaptic connections were accelerated with the secretome-loaded scaffolds.

## Abstract

Although implantation of biomaterials carrying mesenchymal stem cells (MSCs) is considered as a promising strategy for ameliorating neural function after spinal cord injury (SCI), there are still some challenges including poor cell survival rate, tumorigenicity and ethics concerns. The performance of the secretome derived from MSCs was more stable, and its clinical transformation was more operable. Cytokine antibody array demonstrated that the secretome of MSCs contained 79 proteins among the 174 proteins analyzed. Three-dimensional (3D) printed collagen/silk fibroin scaffolds carrying MSCs secretome improved hindlimb locomotor function according to the Basso–Beattie–Bresnahan scores, the inclined-grid climbing test and electrophysiological analysis. Parallel with locomotor function recovery, 3D printed collagen/silk fibroin scaffolds carrying MSCs secretome could further facilitate nerve fiber regeneration, enhance remyelination and accelerate the establishment of synaptic connections at the injury site compared to 3D printed collagen/silk fibroin scaffolds alone group according to magnetic resonance imaging, diffusion tensor imaging, hematoxylin and eosin staining, Bielschowsky’s silver staining, immunofluorescence staining and transmission electron microscopy. These results indicated the implantation of 3D printed collagen/silk fibroin scaffolds carrying MSCs secretome might be a potential treatment for SCI.

## Linked entities

- **Diseases:** spinal cord injury (MONDO:0043797)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Syp (synaptophysin) [NCBI Gene 24804] {aka Syp1}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 29495] {aka Dlgh4, PSD95, Sap90}, CSF2RA (colony stimulating factor 2 receptor subunit alpha) [NCBI Gene 1438] {aka CD116, CDw116, CSF2R, CSF2RAX, CSF2RAY, CSF2RX}, Fgf2 (fibroblast growth factor 2) [NCBI Gene 54250] {aka Fgf-2, Fgf2a, bFGF}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, Mbp (myelin basic protein) [NCBI Gene 24547] {aka Mbps}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, Bdnf (brain-derived neurotrophic factor) [NCBI Gene 24225], THY1 (Thy-1 cell surface antigen) [NCBI Gene 7070] {aka CD90, CDw90}, Ntf3 (neurotrophin 3) [NCBI Gene 81737], PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, Nfasc (neurofascin) [NCBI Gene 116690] {aka NF}, NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}
- **Diseases:** to axon structures (MESH:D020914), Myelination (MESH:D003711), axon loss (MESH:D012183), necrotic (MESH:D009336), functional dysfunction (MESH:D003291), spinal cord (MESH:D013118), SCI (MESH:D013119), CNS disease (MESH:D002493), inflammation (MESH:D007249), neurological deficits (MESH:D009461), infection (MESH:D007239), HUCMSCs (MESH:D015459)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090], Canis lupus familiaris (dog, subspecies) [taxon 9615]
- **Cell lines:** 3D-C — Homo sapiens (Human), Finite cell line (CVCL_U823)

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC9036898/full.md

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Source: https://tomesphere.com/paper/PMC9036898