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A direct role for SNX9 in the biogenesis of filopodia
Author(s) -
Iris K. Jarsch,
Jonathan R Gadsby,
Annalisa Nuccitelli,
Julia Mason,
Hanae Shimo,
Ludovic Pilloux,
N. Bishara Marzook,
Claire M. Mulvey,
Ulrich Dobramysl,
Charles R. Bradshaw,
Kathryn S. Lilley,
Richard D. Hayward,
Tristan J. Vaughan,
Claire Dobson,
Jennifer L. Gallop
Publication year - 2020
Publication title -
the journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.414
H-Index - 380
eISSN - 1540-8140
pISSN - 0021-9525
DOI - 10.1083/jcb.201909178
Subject(s) - filopodia , biology , microbiology and biotechnology , invadopodia , actin , internalization , endocytosis , cell , genetics , cancer cell , cancer
Filopodia are finger-like actin-rich protrusions that extend from the cell surface and are important for cell-cell communication and pathogen internalization. The small size and transient nature of filopodia combined with shared usage of actin regulators within cells confounds attempts to identify filopodial proteins. Here, we used phage display phenotypic screening to isolate antibodies that alter the actin morphology of filopodia-like structures (FLS) in vitro. We found that all of the antibodies that cause shorter FLS interact with SNX9, an actin regulator that binds phosphoinositides during endocytosis and at invadopodia. In cells, we discover SNX9 at specialized filopodia in Xenopus development and that SNX9 is an endogenous component of filopodia that are hijacked by Chlamydia entry. We show the use of antibody technology to identify proteins used in filopodia-like structures, and a role for SNX9 in filopodia.

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