Human Cord Blood-Derived Unrestricted Somatic Stem Cell Infusion Improves Neurobehavioral Outcome in a Rabbit Model of Intraventricular Hemorrhage

Author:

Vinukonda Govindaiah12,Liao Yanling1,Hu Furong1,Ivanova Larisa1,Purohit Deepti3,Finkel Dina A.3,Giri Priyadarshani3,Bapatla Lakshmipramoda2,Shah Shetal13,Zia Muhammed T.3,Hussein Karen13,Cairo Mitchell S.124,La Gamma Edmund F.153

Affiliation:

1. Department of Pediatrics New York Medical College, Valhalla, New York, USA

2. Cell Biology & Anatomy, New York Medical College, Valhalla, New York, USA

3. The Regional Neonatal Center at Maria Fareri Children's Hospital of Westchester Medical Center, Valhalla, New York, USA

4. Department of Medicine, Pathology, Microbiology & Immunology Cell Biology & Anatomy, New York Medical College, Valhalla, New York, USA

5. Department of Biochemistry and Molecular Biology New York Medical College, Valhalla, New York, USA

Abstract

Abstract Intraventricular hemorrhage (IVH) is a severe complication of preterm birth, which leads to hydrocephalus, cerebral palsy, and mental retardation. There are no available therapies to cure IVH, and standard treatment is supportive care. Unrestricted somatic stem cells (USSCs) from human cord blood have reparative effects in animal models of brain and spinal cord injuries. USSCs were administered to premature rabbit pups with IVH and their effects on white matter integrity and neurobehavioral performance were evaluated. USSCs were injected either via intracerebroventricular (ICV) or via intravenous (IV) routes in 3 days premature (term 32d) rabbit pups, 24 hours after glycerol-induced IVH. The pups were sacrificed at postnatal days 3, 7, and 14 and effects were compared to glycerol-treated but unaffected or nontreated control. Using in vivo live bioluminescence imaging and immunohistochemical analysis, injected cells were found in the injured parenchyma on day 3 when using the IV route compared to ICV where cells were found adjacent to the ventricle wall forming aggregates; we did not observe any adverse events from either route of administration. The injected USSCs were functionally associated with attenuated microglial infiltration, less apoptotic cell death, fewer reactive astrocytes, and diminished levels of key inflammatory cytokines (TNFα and IL1β). In addition, we observed better preservation of myelin fibers, increased myelin gene expression, and altered reactive astrocyte distribution in treated animals, and this was associated with improved locomotor function. Overall, our findings support the possibility that USSCs exert anti-inflammatory effects in the injured brain mitigating many detrimental consequences associated with IVH. Stem Cells Translational Medicine  2019;8:1157–1169

Funder

Pediatric Cancer Research Foundation

Boston Children's Health Physicians' Neonatal Division

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

Reference55 articles.

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