Noninvasive and Quantitative Monitoring of Adult Neuronal Stem Cell Migration in Mouse Brain Using Bioluminescence Imaging

Author:

Reumers Veerle12,Deroose Christophe M.134,Krylyshkina Olga4,Nuyts Johan13,Geraerts Martine4,Mortelmans Luc13,Gijsbers Rik14,Van den Haute Chris12,Debyser Zeger14,Baekelandt Veerle12

Affiliation:

1. Molecular Small Animal Imaging Center (MoSAIC), Katholieke Universiteit Leuven, Leuven, Flanders, Belgium

2. Laboratories for Neurobiology and Gene Therapy, Katholieke Universiteit Leuven, Leuven, Flanders, Belgium

3. Division of Nuclear Medicine, Katholieke Universiteit Leuven, Leuven, Flanders, Belgium

4. Laboratories for Molecular Virology and Gene Therapy, Division of Molecular Medicine, Katholieke Universiteit Leuven, Leuven, Flanders, Belgium

Abstract

Abstract It is now generally accepted that continuous neurogenesis occurs in the adult mammalian brain, including that of humans. Modulation of adult neurogenesis can provide therapeutic benefits for various brain disorders, including stroke and Parkinson's disease. The subventricular zone-olfactory bulb pathway is one of the preferred model systems by which to study neural stem cell proliferation, migration, and differentiation in adult rodent brain. Research on adult neurogenesis would greatly benefit from reliable methods for long-term noninvasive in vivo monitoring. We have used lentiviral vectors encoding firefly luciferase to stably mark endogenous neural stem cells in the mouse subventricular zone. We show that bioluminescence imaging (BLI) allows quantitative follow-up of the migration of adult neural stem cells into the olfactory bulb in time. Moreover, we propose a model to fit the kinetic data that allows estimation of migration and survival times of the neural stem cells using in vivo BLI. Long-term expression of brain-derived neurotrophic factor in the subventricular zone attenuated neurogenesis, as detected by histology and BLI. In vivo monitoring of the impact of drugs or genes on adult neurogenesis is now within reach. Disclosure of potential conflicts of interest is found at the end of this article.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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