Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI

PLoS One. 2020 May 26;15(5):e0233263. doi: 10.1371/journal.pone.0233263. eCollection 2020.

Abstract

In the U.S., approximately 1.7 million people suffer traumatic brain injury each year, with many enduring long-term consequences and significant medical and rehabilitation costs. The primary injury causes physical damage to neurons, glia, fiber tracts and microvasculature, which is then followed by secondary injury, consisting of pathophysiological mechanisms including an immune response, inflammation, edema, excitotoxicity, oxidative damage, and cell death. Most attempts at intervention focus on protection, repair or regeneration, with regenerative medicine becoming an intensively studied area over the past decade. The use of stem cells has been studied in many disease and injury models, using stem cells from a variety of sources and applications. In this study, human adipose-derived mesenchymal stromal cells (MSCs) were administered at early (3 days) and delayed (14 days) time points after controlled cortical impact (CCI) injury in rats. Animals were routinely assessed for neurological and vestibulomotor deficits, and at 32 days post-injury, brain tissue was processed by flow cytometry and immunohistochemistry to analyze neuroinflammation. Treatment with HB-adMSC at either 3d or 14d after injury resulted in significant improvements in neurocognitive outcome and a change in neuroinflammation one month after injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology
  • Animals
  • Brain / pathology
  • Brain Injuries, Traumatic / pathology
  • Brain Injuries, Traumatic / psychology
  • Brain Injuries, Traumatic / therapy*
  • Disease Models, Animal
  • Humans
  • Inflammation / pathology
  • Male
  • Maze Learning
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology
  • Motor Skills
  • Neurogenesis
  • Rats, Sprague-Dawley
  • Time Factors

Grants and funding

SDO and CSC have received research support from Hope Bio as part of a sponsored research agreement between Hope Bio and the University of Texas Health Science System (UTHealth). KAR performed the work in this study as an employee of UTHealth, but has since accepted paid employment at Hope Bio. Hope Bio also provided support for this study in the form of salaries for HP and AD. The specific roles of these authors are articulated in the ‘author contributions’ section. Additionally, this study received funding from the Grace Reynolds Wall Research Fund and the Clare A. Glassell Family Pediatric Stem Cell Research Fund. The funders had no role in study design, data collection and analysis, or decision to publish. Hope Biosciences received and approved a draft of the manuscript prior to submission and contributed some minor corrections and additional details for the methods, specifically the ‘Isolation and Expansion of HB-adMSCs’ section.