Nucleobindin-1 regulates ECM degradation by promoting intra-Golgi trafficking of MMPs

Author:

Pacheco-Fernandez Natalia1ORCID,Pakdel Mehrshad1,Blank Birgit2ORCID,Sanchez-Gonzalez Ismael3,Weber Kathrin4ORCID,Tran Mai Ly12,Hecht Tobias Karl-Heinz12ORCID,Gautsch Renate1,Beck Gisela1,Perez Franck5ORCID,Hausser Angelika3ORCID,Linder Stefan4ORCID,von Blume Julia12ORCID

Affiliation:

1. Max Planck Institute of Biochemistry, Martinsried, Germany

2. Department of Cell Biology, Yale University School of Medicine, New Haven, CT

3. Institute of Cell Biology and Immunology, University of Stuttgart, Stuttgart, Germany

4. Institut für Medizinische Mikrobiologie, Virologie und Hygiene, Universitätsklinikum Hamburg, Hamburg, Germany

5. Institute Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France

Abstract

Matrix metalloproteinases (MMPs) degrade several ECM components and are crucial modulators of cell invasion and tissue organization. Although much has been reported about their function in remodeling ECM in health and disease, their trafficking across the Golgi apparatus remains poorly understood. Here we report that the cis-Golgi protein nucleobindin-1 (NUCB1) is critical for MMP2 and MT1-MMP trafficking along the Golgi apparatus. This process is Ca2+-dependent and is required for invasive MDA-MB-231 cell migration as well as for gelatin degradation in primary human macrophages. Our findings emphasize the importance of NUCB1 as an essential component of MMP transport and its overall impact on ECM remodeling.

Funder

Deutscher Akademischer Austauschdienst

Boehringer Ingelheim Fonds

Deutsche Forschungsgemeinschaft

National Institutes of Health

National Institute of General Medical Sciences

Max Planck Institute of Biochemistry

Publisher

Rockefeller University Press

Subject

Cell Biology

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