TY - JOUR
T1 - Fast structural responses of gap junction membrane domains to AB5 toxins
AU - Majoul, Irina V.
AU - Gao, Liang
AU - Betzig, Eric
AU - Onichtchouk, Daria
AU - Butkevich, Eugenia
AU - Kozlov, Yuri
AU - Bukauskas, Feliksas
AU - Bennett, Michael V.L.
AU - Lippincott-Schwartz, Jennifer
AU - Duden, Rainer
PY - 2013/10/29
Y1 - 2013/10/29
N2 - Gap junctions (GJs) represent connexin-rich membrane domains that connect interiors of adjoining cells in mammalian tissues. How fast GJs can respond to bacterial pathogens has not been known previously. Using Bessel beam plane illumination and confocal spinning disk microscopy, we found fast (∼500 ms) formation of connexin-depleted regions (CDRs) inside GJ plaques between cells exposed to AB5 toxins. CDR formation appears as a fast redistribution of connexin channels within GJ plaques with minor changes in outline or geometry. CDR formation does not depend on membrane trafficking or submembrane cytoskeleton and has no effect on GJ conductance. However, CDR responses depend on membrane lipids, can be modified by cholesterol-clustering agents and extracellular K+ ion concentration, and influence cAMP signaling. The CDR response of GJ plaques to bacterial toxins is a phenomenon observed for all tested connexin isoforms. Through signaling, the CDR response may enable cells to sense exposure to AB5 toxins. CDR formation may reflect lipid-phase separation events in the biological membrane of the GJ plaque, leading to increased connexin packing and lipid reorganization. Our data demonstrate very fast dynamics (in the millisecond-To-second range) within GJ plaques, which previously were considered to be relatively stable, long-lived structures.
AB - Gap junctions (GJs) represent connexin-rich membrane domains that connect interiors of adjoining cells in mammalian tissues. How fast GJs can respond to bacterial pathogens has not been known previously. Using Bessel beam plane illumination and confocal spinning disk microscopy, we found fast (∼500 ms) formation of connexin-depleted regions (CDRs) inside GJ plaques between cells exposed to AB5 toxins. CDR formation appears as a fast redistribution of connexin channels within GJ plaques with minor changes in outline or geometry. CDR formation does not depend on membrane trafficking or submembrane cytoskeleton and has no effect on GJ conductance. However, CDR responses depend on membrane lipids, can be modified by cholesterol-clustering agents and extracellular K+ ion concentration, and influence cAMP signaling. The CDR response of GJ plaques to bacterial toxins is a phenomenon observed for all tested connexin isoforms. Through signaling, the CDR response may enable cells to sense exposure to AB5 toxins. CDR formation may reflect lipid-phase separation events in the biological membrane of the GJ plaque, leading to increased connexin packing and lipid reorganization. Our data demonstrate very fast dynamics (in the millisecond-To-second range) within GJ plaques, which previously were considered to be relatively stable, long-lived structures.
UR - http://www.scopus.com/inward/record.url?scp=84887038542&partnerID=8YFLogxK
U2 - 10.1073/pnas.1315850110
DO - 10.1073/pnas.1315850110
M3 - Journal articles
C2 - 24133139
AN - SCOPUS:84887038542
SN - 0027-8424
VL - 110
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 44
ER -