Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1)

Superresolution architecture of cornerstone focal adhesions in human pluripotent stem cells




Julkaisun tekijät: Aki Stubb, Camilo Guzmán, Elisa Närvä, Jesse Aaron, Teng-Leong Chew, Markku Saari, Mitro Miihkinen, Guillaume Jacquemet, Johanna Ivaska

Kustantaja: Nature Publishing Group

Julkaisuvuosi: 2019

Journal: Nature Communications

Tietokannassa oleva lehden nimi: Nature Communications

Volyymi: 10

Julkaisunumero: 1

Sivujen määrä: 15

ISSN: 2041-1723

eISSN: 2041-1723

DOI: http://dx.doi.org/10.1038/s41467-019-12611-w

Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/43310710


Tiivistelmä

While it is clear that key transcriptional programmes are important for maintaining pluripotency, the requirement for cell adhesion to the extracellular matrix remains poorly defined. Human pluripotent stem cells (hPSCs) form colonies encircled by an actin ring and large stable cornerstone focal adhesions (FA). Using superresolution two-colour interferometric photo-activated localisation microscopy, we examine the three-dimensional architecture of cornerstone adhesions and report vertical lamination of FA proteins with three main structural features distinct from previously studied focal adhesions: 1) integrin β5 and talin are present at high density, at the edges of cornerstone FA, adjacent to a vertical kank-rich protein wall, 2) vinculin localises higher than previously reported, displaying a head-above-tail orientation, and 3) surprisingly, actin and α-actinin are present in two discrete z-layers. Finally, we report that depletion of kanks diminishes FA patterning, and actin organisation within the colony, indicating a role for kanks in hPSC colony architecture.


Ladattava julkaisu

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.




Last updated on 2022-07-04 at 16:15