The Disintegrin/Metalloproteinase ADAM10 Is Essential for the Establishment of the Brain Cortex

Ellen Jorissen(Vlaams Instituut voor Biotechnologie), Johannes Prox(Christian-Albrechts-Universität zu Kiel), Christian Bernreuther(Universität Hamburg), Silvio Weber(Christian-Albrechts-Universität zu Kiel), Ralf Schwanbeck(Christian-Albrechts-Universität zu Kiel), Lutgarde Serneels(Vlaams Instituut voor Biotechnologie), An Snellinx(Vlaams Instituut voor Biotechnologie), Katleen Craessaerts(Vlaams Instituut voor Biotechnologie), Amantha Thathiah(Vlaams Instituut voor Biotechnologie), Ina Tesseur(Vlaams Instituut voor Biotechnologie), Udo Bartsch(Universität Hamburg), Gisela Weskamp(Hospital for Special Surgery), Carl Blobel(Hospital for Special Surgery), Markus Glatzel(Universität Hamburg), Bart De Strooper(Vlaams Instituut voor Biotechnologie), Paul Säftig(Christian-Albrechts-Universität zu Kiel)
Journal of Neuroscience
April 6, 2010
Cited by 355Open Access
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Abstract

The metalloproteinase and major amyloid precursor protein (APP) alpha-secretase candidate ADAM10 is responsible for the shedding of proteins important for brain development, such as cadherins, ephrins, and Notch receptors. Adam10(-/-) mice die at embryonic day 9.5, due to major defects in development of somites and vasculogenesis. To investigate the function of ADAM10 in brain, we generated Adam10 conditional knock-out (cKO) mice using a Nestin-Cre promotor, limiting ADAM10 inactivation to neural progenitor cells (NPCs) and NPC-derived neurons and glial cells. The cKO mice die perinatally with a disrupted neocortex and a severely reduced ganglionic eminence, due to precocious neuronal differentiation resulting in an early depletion of progenitor cells. Premature neuronal differentiation is associated with aberrant neuronal migration and a disorganized laminar architecture in the neocortex. Neurospheres derived from Adam10 cKO mice have a disrupted sphere organization and segregated more neurons at the expense of astrocytes. We found that Notch-1 processing was affected, leading to downregulation of several Notch-regulated genes in Adam10 cKO brains, in accordance with the central role of ADAM10 in this signaling pathway and explaining the neurogenic phenotype. Finally, we found that alpha-secretase-mediated processing of APP was largely reduced in these neurons, demonstrating that ADAM10 represents the most important APP alpha-secretase in brain. Our study reveals that ADAM10 plays a central role in the developing brain by controlling mainly Notch-dependent pathways but likely also by reducing surface shedding of other neuronal membrane proteins including APP.


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