Human adipose-derived mesenchymal stem cells for acute and sub-acute TBI.
Katherine A RuppertKarthik S PrabhakaraNaama E Toledano-FurmanSanjna UdthaAustin Q ArceneauxHyeonggeun ParkAn DaoCharles S CoxScott D OlsonPublished in: PloS one (2020)
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.
Keyphrases
- traumatic brain injury
- stem cells
- mesenchymal stem cells
- immune response
- cell death
- endothelial cells
- flow cytometry
- healthcare
- randomized controlled trial
- bone marrow
- cognitive impairment
- physical activity
- umbilical cord
- cerebral ischemia
- intensive care unit
- brain injury
- blood brain barrier
- multiple sclerosis
- bipolar disorder
- neuropathic pain
- functional connectivity
- resting state
- smoking cessation