Human Adult Dental Pulp Stem Cells Enhance Poststroke Functional Recovery Through Non-Neural Replacement Mechanisms

Author:

Leong Wai Khay12,Henshall Tanya L.3,Arthur Agnes13,Kremer Karlea L.12,Lewis Martin D.12,Helps Stephen C.4,Field John5,Hamilton-Bruce Monica A.6,Warming Scott2,Manavis Jim7,Vink Robert4,Gronthos Stan13,Koblar Simon A.156

Affiliation:

1. Centre for Stem Cell Research, Robinson Institute, University of Adelaide, Adelaide, South Australia, Australia

2. School of Molecular and Biomedical Science, University of Adelaide, Adelaide, South Australia, Australia

3. Division of Hematology, Hanson Institute, SA Pathology, Adelaide, South Australia, Australia

4. School of Medical Science, University of Adelaide, Adelaide, South Australia, Australia

5. School of Medicine, University of Adelaide, Adelaide, South Australia, Australia

6. Department of Neurology, Queen Elizabeth Hospital, Woodville, South Australia, Australia

7. Centre for Neurological Diseases, Hanson Institute, SA Pathology, Adelaide, South Australia, Australia

Abstract

Abstract Human adult dental pulp stem cells (DPSCs), derived from third molar teeth, are multipotent and have the capacity to differentiate into neurons under inductive conditions both in vitro and following transplantation into the avian embryo. In this study, we demonstrate that the intracerebral transplantation of human DPSCs 24 hours following focal cerebral ischemia in a rodent model resulted in significant improvement in forelimb sensorimotor function at 4 weeks post-treatment. At this time, 2.3 ± 0.7% of engrafted cells had survived in the poststroke brain and demonstrated targeted migration toward the stroke lesion. In the peri-infarct striatum, transplanted DPSCs differentiated into astrocytes in preference to neurons. Our data suggest that the dominant mechanism of action underlying DPSC treatment that resulted in enhanced functional recovery is unlikely to be due to neural replacement. Functional improvement is more likely to be mediated through DPSC-dependent paracrine effects. This study provides preclinical evidence for the future use of human DPSCs in cell therapy to improve outcome in stroke patients.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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