β1 integrins activate a MAPK signalling pathway in neural stem cells that contributes to their maintenance
Author:
Campos Lia S.1, Leone Dino P.2, Relvas Joao B.12, Brakebusch Cord3, Fässler Reinhard3, Suter Ueli2, ffrench-Constant Charles1
Affiliation:
1. Departments of Medical Genetics and Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK 2. Institute of Cell Biology, Department of Biology, Swiss Federal Institute of Technology, ETH Hönggerberg, CH-8093 Zürich, Switzerland 3. Department of Molecular Medicine, Max-Planck-Institut für Biochemie, Am Klopferspitz 18a, D-82152 Martinsried, Germany
Abstract
The emerging evidence that stem cells develop in specialised niches highlights the potential role of environmental factors in their regulation. Here we examine the role of β1 integrin/extracellular matrix interactions in neural stem cells. We find high levels of β1 integrin expression in the stem-cell containing regions of the embryonic CNS, with associated expression of the laminin α2 chain. Expression levels of lamininα2 are reduced in the postnatal CNS, but a population of cells expressing high levels of β1 remains. Using neurospheres –aggregate cultures, derived from single stem cells, that have a three-dimensional architecture that results in the localisation of the stem cell population around the edge of the sphere – we show directly thatβ1 integrins are expressed at high levels on neural stem cells and can be used for their selection. MAPK, but not PI3K, signalling is required for neural stem cell maintenance, as assessed by neurosphere formation, and inhibition or genetic ablation of β1 integrin using cre/lox technology reduces the level of MAPK activity. We conclude that integrins are therefore an important part of the signalling mechanisms that control neural stem cell behaviour in specific areas of the CNS.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
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