Regenerative potential of primary adult human neural stem cells on micropatterned bio-implants boosts motor recovery

被引:17
作者
Davoust, Carole [1 ]
Plas, Benjamin [1 ,3 ]
Beduer, Amelie [2 ]
Demain, Boris [1 ]
Salabert, Anne-Sophie [1 ,3 ]
Sol, Jean Christophe [1 ,3 ]
Vieu, Christophe [2 ]
Vaysse, Laurence [1 ]
Loubinoux, Isabelle [1 ,4 ]
机构
[1] Univ Toulouse, Toulouse NeuroImaging Ctr, ToNIC, INSERM,UPS, Toulouse, France
[2] Univ Toulouse, CNRS, UPS, IAAS CNRS,INSA, Toulouse, France
[3] CHU Toulouse, Pole Neurosci, Toulouse, France
[4] CHU Purpan, Inserm UPS ToNIC UMR1214, Pavillon Baudot,Pl Dr Baylac, F-31024 Toulouse 3, France
来源
STEM CELL RESEARCH & THERAPY | 2017年 / 8卷
关键词
Brain injury; Cell therapy; Biomaterial; Tissue engineering; Sensorimotor recovery; HUMAN PROGENITOR CELLS; MARROW STROMAL CELLS; NEUROBLAST MIGRATION; FUNCTIONAL RECOVERY; COLLAGEN SCAFFOLDS; BRAIN-LESION; NEUROGENESIS; DIFFERENTIATION; TRANSPLANTATION; ISCHEMIA;
D O I
10.1186/s13287-017-0702-3
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: The adult brain is unable to regenerate itself sufficiently after large injuries. Therefore, hopes rely on therapies using neural stem cell or biomaterial transplantation to sustain brain reconstruction. The aim of the present study was to evaluate the improvement in sensorimotor recovery brought about by human primary adult neural stem cells (hNSCs) in combination with bio-implants. Methods: hNSCs were pre-seeded on implants micropatterned for neurite guidance and inserted intracerebrally 2 weeks after a primary motor cortex lesion in rats. Long-term behaviour was significantly improved after hNSC implants versus cell engraftment in the grip strength test. MRI and immunohistological studies were conducted to elucidate the underlying mechanisms of neuro-implant integration. Results: hNSC implants promoted tissue reconstruction and limited hemispheric atrophy and glial scar expansion. After 3 months, grafted hNSCs were detected on implants and expressed mature neuronal markers (NeuN, MAP2, SMI312). They also migrated over a short distance to the reconstructed tissues and to the peri-lesional tissues, where 26% integrated as mature neurons. Newly formed host neural progenitors (nestin, DCX) colonized the implants, notably in the presence of hNSCs, and participated in tissue reconstruction. The microstructured bio-implants sustained the guided maturation of both grafted hNSCs and endogenous progenitors. Conclusions: These immunohistological results are coherent with and could explain the late improvement observed in sensorimotor recovery. These findings provide novel insights into the regenerative potential of primary adult hNSCs combined with microstructured implants.
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页数:14
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