Open AccessMembrane distribution of epidermal growth factor receptors in cells expressing different gangliosides
Author(s) -
Zurita Adolfo R.,
Crespo Pilar M.,
Koritschoner Nicolás P.,
Daniotti José L.
Publication year - 2004
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.2004.04165.x
Subject(s) - ganglioside , lipid raft , epidermal growth factor receptor , microbiology and biotechnology , glycolipid , epidermal growth factor , receptor , endogeny , membrane , glycosphingolipid , cell surface receptor , chinese hamster ovary cell , biology , cell membrane , chemistry , biochemistry , signal transduction
Gangliosides have been found to reside in glycosphingolipid‐enriched microdomains (GEM) of the plasma membrane and to be involved in the regulation of epidermal growth factor receptor (EGFr or ErbB1) activity. To gain further insight into the mechanisms involved in EGFr modulation by gangliosides, we investigated the distribution of EGFr family members in the plasma membrane of CHO‐K1 cells, which were genetically modified to express different ganglioside molecules or depleted of glycolipids. Our data demonstrate that at least four different sets of endogenously expressed gangliosides, including GD3, did not have a significant effect on EGFr distribution in the plasma membrane. In addition, using confocal microscopy analysis we clearly demonstrated that the EGFr co‐localizes only to a minor extent with GD3. We also explored the endogenous expression, in wild‐type CHO‐K1 cells, of the orphan receptor ErbB2 (which is the preferred heteroassociation partner of all other ErbB proteins) and the effect of GD3 expression on its membrane distribution. Our results showed that CHO‐K1 cells endogenously express ErbB2 and that expression of the GD3 affected, to some extent, the membrane distribution of endogenous ErbB2. Finally, our findings support the notion that most EGFr are excluded from GEM, while an important fraction of ErbB2 is found to be associated with these microdomains in membranes from CHO‐K1 cells.