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Implantation of Neuronal Stem Cells Enhances Object Recognition without Increasing Neurogenesis after Lateral Fluid Percussion Injury in Mice

  • Laura B. Ngwenya
  • , Sarmistha Mazumder
  • , Zachary R. Porter
  • , Amy Minnema
  • , Duane J. Oswald
  • , H. Francis Farhadi

Producción científica: Articlerevisión exhaustiva

13 Citas (Scopus)

Resumen

Cognitive deficits after traumatic brain injury (TBI) are debilitating and contribute to the morbidity and loss of productivity of over 10 million people worldwide. Cell transplantation has been linked to enhanced cognitive function after experimental traumatic brain injury, yet the mechanism of recovery is poorly understood. Since the hippocampus is a critical structure for learning and memory, supports adult neurogenesis, and is particularly vulnerable after TBI, we hypothesized that stem cell transplantation after TBI enhances cognitive recovery by modulation of endogenous hippocampal neurogenesis. We performed lateral fluid percussion injury (LFPI) in adult mice and transplanted embryonic stem cell-derived neural progenitor cells (NPC). Our data confirm an injury-induced cognitive deficit in novel object recognition, a hippocampal-dependent learning task, which is reversed one week after NPC transplantation. While LFPI alone promotes hippocampal neurogenesis, as revealed by doublecortin immunolabeling of immature neurons, subsequent NPC transplantation prevents increased neurogenesis and is not associated with morphological maturation of endogenous injury-induced immature neurons. Thus, NPC transplantation enhances cognitive recovery early after LFPI without a concomitant increase in neuron numbers or maturation.

Idioma originalEnglish
Número de artículo4209821
PublicaciónStem Cells International
Volumen2018
DOI
EstadoPublished - 2018

Nota bibliográfica

Publisher Copyright:
© 2018 Laura B. Ngwenya et al.

Financiación

The authors acknowledge Drs. Ashley Fenn and Jonathan Godbout for establishing the fluid percussion injury model at The Ohio State University. The authors would like to thank Amy Tovar and members of the laboratories of Drs. Philip Popovich and Dana McTigue for helpful discussions and input in designing and administering the behavioral studies. The authors thank the Center for Brain and Spinal Cord Repair at The Ohio State University for use of surgical and behavioral equipment and resources. The authors also thank Lesley Fisher and the laboratory of Dr. Michelle Basso for allowing use of the Stereo Investigator Microscopy and Software. Confocal images were acquired using the Campus Microscopy and Imaging Facility at The Ohio State University. HFF received funding support from The Ohio State University Neurosignature Program, Center for Clinical and Translational Science (UL1TR000090), and a P30 Core Grant NINDS P30-NS045758. Funding support was in part also provided through a University of Cincinnati Gardner Neuroscience Institute Research Pilot grant (to Laura B. Ngwenya).

FinanciadoresNúmero del financiador
Ohio State University Neurosignature Program
University of Cincinnati Gardner Neuroscience Institute
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilP30-NS045758
Center for Clinical and Translational Science, University of Illinois at ChicagoUL1TR000090

    ASJC Scopus subject areas

    • Molecular Biology
    • Cell Biology

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