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Injury-Transplantation Interval-Dependent Amelioration of Axonal Degeneration and Motor Deficit in Rats with Penetrating Traumatic Brain Injury.

Authors :
Andreu M
Sanchez LMQ
Spurlock MS
Hu Z
Mahavadi A
Powell HR
Lujan MM
Nodal S
Cera M
Ciocca I
Bullock R
Gajavelli S
Source :
Neurotrauma reports [Neurotrauma Rep] 2023 Apr 10; Vol. 4 (1), pp. 225-235. Date of Electronic Publication: 2023 Apr 10 (Print Publication: 2023).
Publication Year :
2023

Abstract

Penetrating traumatic brain injury (pTBI) is increasingly survivable, but permanently disabling as adult mammalian nervous system does not regenerate. Recently, our group demonstrated transplant location-dependent neuroprotection and safety of clinical trial-grade human neural stem cell (hNSC) transplantation in a rodent model of acute pTBI. To evaluate whether longer injury-transplantation intervals marked by chronic inflammation impede engraftment, 60 male Sprague-Dawley rats were randomized to three sets. Each set was divided equally into two groups: 1) with no injury (sham) or 2) pTBI. After either 1 week (groups 1 and 2), 2 weeks (groups 3 and 4), or 4 weeks after injury (groups 5 and 6), each animal received 0.5 million hNSCs perilesionally. A seventh group of pTBI animals treated with vehicle served as the negative control. All animals were allowed to survive 12 weeks with standard chemical immunosuppression. Motor capacity was assessed pre-transplant to establish injury-induced deficit and followed by testing at 8 and 12 weeks after transplantation. Animals were euthanized, perfused, and examined for lesion size, axonal degeneration, and engraftment. Compared to vehicle, transplanted groups showed a trend for reduced lesion size and axonal injury across intervals. Remote secondary axonal injury was significantly reduced in groups 2 and 4, but not in group 6. The majority of animals showed robust engraftment independent of the injury-transplant time interval. Modest amelioration of motor deficit paralleled the axonal injury trend. In aggregate, pTBI-induced remote secondary axonal injury was resolved by early, but not delayed, hNSC transplantation.<br />Competing Interests: The human neural stem cells (GFP labeled NSI-566 RSC) were provided by Dr. Karl Johe and Dr. Thomas G. Hazel, employees of NeuralStem Inc. (Germantown, MD). Dr. Gajavelli is an employee of Lacerta Therapeutics, a company developing viral vector-based gene therapies for central nervous system disorders.<br /> (© MaryLourdes Andreu et al., 2023; Published by Mary Ann Liebert, Inc.)

Details

Language :
English
ISSN :
2689-288X
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
Neurotrauma reports
Publication Type :
Academic Journal
Accession number :
37095855
Full Text :
https://doi.org/10.1089/neur.2022.0087