Tetraspanin 4 mediates migrasome formation via a two-stage mechanism

Migrasomes are recently discovered signalling organelles, enriched with tetraspanin proteins (TSPAN)1. They form by local swelling of retraction fibers, the cylindrical protrusions of cell membranes that form as a result of cell migration along external substrates. Migrasomes can grow up to several micrometers in diameter2, and allow cells to release contents such as chemokines at specific locations, hence, transmitting signals to surrounding cells through the relevant chemokine receptors. Recently, evidence emerged showing that migrasomes play essential roles in fundamental cellular processes such transfer of mRNA and proteins3, organ morphogenesis4, and mitochondria quality control5. Thus, understanding the mechanism of migrasome biogenesis is of outstanding importance. Previously, it was established that the molecules crucial for migrasome formation are tetraspanin proteins and cholesterol forming macrodomains in the migrasome membrane, while the physical forces driving local swelling of the retraction fibers originate from membrane tension and bending rigidity1. Yet, it remained unknown how and in which time sequence these factors are involved in migrasome nucleation, growth, and stabilization, and what are the possible intermediate stages of migrasome biogenesis.

[1]  Xiaoyu Hu,et al.  Mitocytosis, a migrasome-mediated mitochondrial quality-control process , 2021, Cell.

[2]  Xuerui Yang,et al.  Lateral transfer of mRNA and protein by migrasomes modifies the recipient cells , 2020, Cell research.

[3]  O. Nureki,et al.  Structural insights into tetraspanin CD9 function , 2020, Nature Communications.

[4]  P. Kuzmin,et al.  Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon , 2019, Nature Communications.

[5]  Yuling Chen,et al.  Migrasomes provide regional cues for organ morphogenesis during zebrafish gastrulation , 2019, Nature Cell Biology.

[6]  M. Kozlov,et al.  Migrasome formation is mediated by assembly of micron-scale tetraspanin macrodomains , 2019, Nature Cell Biology.

[7]  Y. Li,et al.  Discovery of the migrasome, an organelle mediating release of cytoplasmic contents during cell migration , 2014, Cell Research.

[8]  P. Schwille,et al.  Model membrane platforms to study protein-membrane interactions , 2012, Molecular membrane biology.

[9]  M. Tomlinson,et al.  The emerging role of tetraspanin microdomains on endothelial cells. , 2011, Biochemical Society transactions.

[10]  P. Bassereau,et al.  ArfGAP1 generates an Arf1 gradient on continuous lipid membranes displaying flat and curved regions , 2010, The EMBO journal.

[11]  Eric Rubinstein,et al.  Lateral organization of membrane proteins: tetraspanins spin their web. , 2009, The Biochemical journal.

[12]  A. Callan-Jones,et al.  Curvature-driven lipid sorting needs proximity to a demixing point and is aided by proteins , 2009, Proceedings of the National Academy of Sciences.

[13]  W. Webb,et al.  Fluorescence probe partitioning between Lo/Ld phases in lipid membranes. , 2007, Biochimica et biophysica acta.

[14]  C. Boucheix,et al.  Membrane microdomains and proteomics: Lessons from tetraspanin microdomains and comparison with lipid rafts , 2006, Proteomics.

[15]  Moses,et al.  Instability and "pearling" states produced in tubular membranes by competition of curvature and tension. , 1994, Physical review letters.

[16]  Evans,et al.  Entropy-driven tension and bending elasticity in condensed-fluid membranes. , 1990, Physical review letters.

[17]  S. Veatch,et al.  Giant Plasma Membrane Vesicles: An Experimental Tool for Probing the Effects of Drugs and Other Conditions on Membrane Domain Stability. , 2018, Methods in enzymology.