دورية أكاديمية

Runx1 promotes proliferation and neuronal differentiation in adult mouse neurosphere cultures

التفاصيل البيبلوغرافية
العنوان: Runx1 promotes proliferation and neuronal differentiation in adult mouse neurosphere cultures
المؤلفون: T.T. Logan, M. Rusnak, A.J. Symes
المصدر: Stem Cell Research, Vol 15, Iss 3, Pp 554-564 (2015)
بيانات النشر: Elsevier, 2015.
سنة النشر: 2015
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: Runx1, AML1, Adult neural stem cells, Neurosphere, Proliferation, Neuronal differentiation, Biology (General), QH301-705.5
الوصف: Traumatic brain injury alters the signaling environment of the adult neurogenic niche and may activate unique proliferative cell populations that contribute to the post-injury neurogenic response. Runx1 is not normally expressed by adult neural stem or progenitor cells (NSPCs) but is induced in a subpopulation of putative NSPCs after brain injury in adult mice. In order to investigate the role of Runx1 in NSPCs, we established neurosphere cultures of adult mouse subventricular zone NSPCs. We show that Runx1 is basally expressed in neurosphere culture. Removal of the mitogen bFGF or addition of 1% FBS decreased Runx1 expression. Inhibition of endogenous Runx1 activity with either Ro5-3335 or shRNA-mediated Runx1 knockdown inhibited NSPC proliferation without affecting differentiation. Lentiviral mediated over-expression of Runx1 in neurospheres caused a significant change in cell morphology without reducing proliferation. Runx1-overexpressing neurospheres changed from floating spheres to adherent colonies or individual unipolar or bipolar cells. Flow cytometry analysis indicated that Runx1 over-expression produced a significant increase in expression of the neuronal marker TuJ1 and a minor increase in the astrocytic marker S100β. Thus, Runx1 expression drove adult NSPC differentiation, predominantly toward a neuronal lineage. These data suggest that Runx1 could be manipulated after injury to promote neuronal differentiation to facilitate repair of the CNS.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1873-5061
1876-7753
Relation: http://www.sciencedirect.com/science/article/pii/S1873506115001336; https://doaj.org/toc/1873-5061; https://doaj.org/toc/1876-7753
DOI: 10.1016/j.scr.2015.09.014
URL الوصول: https://doaj.org/article/b54756ab76e2478a9543f90e7afc4450
رقم الأكسشن: edsdoj.b54756ab76e2478a9543f90e7afc4450
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18735061
18767753
DOI:10.1016/j.scr.2015.09.014