TY - JOUR
T1 - Neural stem/progenitor cell-laden microfibers promote transplant survival in a mouse transected spinal cord injury model
AU - Sugai, Keiko
AU - Nishimura, Soraya
AU - Kato-Negishi, Midori
AU - Onoe, Hiroaki
AU - Iwanaga, Shintaroh
AU - Toyama, Yoshiaki
AU - Matsumoto, Morio
AU - Takeuchi, Shoji
AU - Okano, Hideyuki
AU - Nakamura, Masaya
N1 - Publisher Copyright:
© 2015 Wiley Periodicals, Inc.
PY - 2015/12
Y1 - 2015/12
N2 - Previous studies have demonstrated that transplantation of neural stem/progenitor cells (NS/PCs) into the lesioned spinal cord can promote functional recovery following incomplete spinal cord injury (SCI) in animal models. However, this strategy is insufficient following complete SCI because of the gap at the lesion epicenter. To obtain functional recovery in a mouse model of complete SCI, this study uses a novel collagen-based microfiber as a scaffold for engrafted NS/PCs. We hypothesized that the NS/PC-microfiber combination would facilitate lesion closure as well as transplant survival in the transected spinal cord. NS/PCs were seeded inside the novel microfibers, where they maintained their capacity to differentiate and proliferate. After transplantation, the stumps of the transected spinal cord were successfully bridged by the NS/PC-laden microfibers. Moreover, the transplanted cells migrated into the host spinal cord and differentiated into three neural lineages (astrocytes, neurons, and oligodendrocytes). However, the NS/PC-laden scaffold could not achieve a neural connection between the rostral end of the injury and the intact caudal area of the spinal cord, nor could it achieve recovery of motor function. To obtain optimal functional recovery, a microfiber design with a modified composition may be useful. Furthermore, combinatorial therapy with rehabilitation and/or medications should also be considered for practical success of biomaterial/cell transplantation-based approaches to regenerative medicine.
AB - Previous studies have demonstrated that transplantation of neural stem/progenitor cells (NS/PCs) into the lesioned spinal cord can promote functional recovery following incomplete spinal cord injury (SCI) in animal models. However, this strategy is insufficient following complete SCI because of the gap at the lesion epicenter. To obtain functional recovery in a mouse model of complete SCI, this study uses a novel collagen-based microfiber as a scaffold for engrafted NS/PCs. We hypothesized that the NS/PC-microfiber combination would facilitate lesion closure as well as transplant survival in the transected spinal cord. NS/PCs were seeded inside the novel microfibers, where they maintained their capacity to differentiate and proliferate. After transplantation, the stumps of the transected spinal cord were successfully bridged by the NS/PC-laden microfibers. Moreover, the transplanted cells migrated into the host spinal cord and differentiated into three neural lineages (astrocytes, neurons, and oligodendrocytes). However, the NS/PC-laden scaffold could not achieve a neural connection between the rostral end of the injury and the intact caudal area of the spinal cord, nor could it achieve recovery of motor function. To obtain optimal functional recovery, a microfiber design with a modified composition may be useful. Furthermore, combinatorial therapy with rehabilitation and/or medications should also be considered for practical success of biomaterial/cell transplantation-based approaches to regenerative medicine.
KW - Biomaterial
KW - Microfiber
KW - Neural stem/progenitor cell
KW - Spinal cord injury
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U2 - 10.1002/jnr.23636
DO - 10.1002/jnr.23636
M3 - Article
C2 - 26301451
AN - SCOPUS:84945492895
SN - 0360-4012
VL - 93
SP - 1826
EP - 1838
JO - Journal of Neuroscience Research
JF - Journal of Neuroscience Research
IS - 12
ER -