ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death

Author:

Raab Matthew12,Gentili Matteo3,de Belly Henry1,Thiam Hawa-Racine1,Vargas Pablo12,Jimenez Ana Joaquina1,Lautenschlaeger Franziska1,Voituriez Raphaël45,Lennon-Duménil Ana-Maria3,Manel Nicolas3,Piel Matthieu12

Affiliation:

1. Institut Curie, PSL Research University, CNRS, UMR 144, F-75005 Paris, France.

2. Institut Pierre-Gilles de Gennes, PSL Research University, F-75005 Paris, France.

3. Institut Curie, PSL Research University, INSERM, U 932, F-75005 Paris, France.

4. Laboratoire de Physique Théorique de la Matière Condensée, CNRS UMR 7600, Université Pierre et Marie Curie, Paris, France.

5. Laboratoire Jean Perrin, CNRS UMR 8237, Université Pierre et Marie Curie, Paris, France.

Abstract

Repairing tears in the nuclear envelope The nuclear envelope segregates genomic DNA from the cytoplasm and regulates protein trafficking between the cytosol and the nucleus. Maintaining nuclear envelope integrity during interphase is considered crucial. However, Raab et al. and Denais et al. show that migrating immune and cancer cells experience frequent and transitory nuclear envelope ruptures when they move through tight spaces (see the Perspective by Burke). The nuclear envelope reseals rapidly during interphase, assisted by components of the ESCRT III membrane-remodeling machinery. Science , this issue pp. 359 and 353 ; see also p. 295

Funder

European Research Council (ERC)

Human Frontier Science Program

Agence Nationale de Research

ERC

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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