Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair

• Published in: Nature communications Vol. 8; no. 1; pp. 1623 - 11
• Main Authors: Boye, Theresa Louise, Maeda, Kenji, Pezeshkian, Weria, Sønder, Stine Lauritzen, Haeger, Swantje Christin, Gerke, Volker, Simonsen, Adam Cohen, Nylandsted, Jesper
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 20.11.2017; Nature Publishing Group UK; Nature Portfolio
• Subjects: Annexin A4 - genetics; Annexin A4 - metabolism; Annexin A6 - genetics; Annexin A6 - metabolism; Binding sites; Calcium - metabolism; Calcium influx; Cancer; Cell Membrane - chemistry; Cell Membrane - genetics; Cell Membrane - metabolism; Cloning; CRISPR; Curvature; Gene expression; HeLa Cells; Humans; Injuries; Lasers; Membranes; Membranes, Artificial; Micrometers; Phospholipids; Phospholipids - metabolism; Plasma; Proteins; Repair; Wound Healing; Wounds
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-017-01743-6

Efficient cell membrane repair mechanisms are essential for maintaining membrane integrity and thus for cell life. Here we show that the Ca - and phospholipid-binding proteins annexin A4 and A6 are involved in plasma membrane repair and needed for rapid closure of micron-size holes. We demonstrate that annexin A4 binds to artificial membranes and generates curvature force initiated from free edges, whereas annexin A6 induces constriction force. In cells, plasma membrane injury and Ca influx recruit annexin A4 to the vicinity of membrane wound edges where its homo-trimerization leads to membrane curvature near the edges. We propose that curvature force is utilized together with annexin A6-mediated constriction force to pull the wound edges together for eventual fusion. We show that annexin A4 can counteract various plasma membrane disruptions including holes of several micrometers indicating that induction of curvature force around wound edges is an early key event in cell membrane repair.