TY - JOUR
T1 - Caveolin-mediated regulation of signaling along the p42/44 MAP kinase cascade in vivo
T2 - A role for the caveolin-scaffolding domain
AU - Engelman, Jeffrey A.
AU - Chu, Caryn
AU - Lin, Anning
AU - Jo, Hanjoong
AU - Ikezu, Tsuneya
AU - Okamoto, Takashi
AU - Kohtz, D. Stave
AU - Lisanti, Michael P.
N1 - Funding Information:
We thank Drs. G.N. Gill, C. Marshall, R. Krauss, M. Weber, R. Treisman for generously donating a variety of cDNA constructions. This work was supported by an NIH FIRST Award (GM-50443; to M.P.L.), and grants from the G. Harold and Leila Y. Mathers Charitable Foundation (to M.P.L.) and the Charles E. Culpeper Foundation (to M.P.L.). J.A.E. was supported by an NIH Medical Scientist Training Program Grant T32-GM07288. H.J. is supported by an NIH FIRST Award (HL-53601) and an American Heart Association Grant-In-Aid (AL-G-960035). A.L. is supported by an NIH grant (CA73740) and an American Heart Association Scientist Development grant (9630261N). T.O. is supported by an NIH FIRST Award (MH-56036). T.I. is a fellow of JSPS for Research Abroad. D.S.K. was supported by an NIH Grant CA-72775 and a Grant-In-Aid from the American Heart Association.
PY - 1998/5/29
Y1 - 1998/5/29
N2 - The p42/44 mitogen-activated protein (MAP)-kinase cascade is a well- established signal transduction pathway that is initiated at the cell surface and terminates within the nucleus. More specifically, receptor tyrosine kinases can indirectly activate Raf, which in turn leads to activation of MEK and ERK and ultimately phosphorylation of Elk, a nuclear transcription factor. Recent reports have suggested that some members of p42/44 MAP kinase cascade can be sequestered within plasmalemmal caveolae in vivo. For example, morphological studies have directly shown that ERK-1/2 is concentrated in plasma membrane caveolae in vivo using immunoelectron microscopy. In addition, constitutive activation of the p42/44 MAP kinase cascade is sufficient to reversibly down-regulate caveolin-1 mRNA and protein expression. However, the functional relationship between the p42/44 MAP kinase cascade and caveolins remains unknown. Here, we examine the in vivo role of caveolins in regulating signaling along the MAP kinase cascade. We find that co-expression with caveolin 1 dramatically inhibits signaling from EGF-R, Raf, MEK-1 and ERK-2 to the nucleus. Using a variety of caveolin-1 deletion mutants, we mapped this in vivo inhibitory activity to caveolin-1 residues 32-95. Peptides derived from this region of caveolin 1 also inhibit the in vitro kinase activity of purified MEK-1 and ERK-2. Thus, we show here that caveolin-1 expression can inhibit signal transduction from the p42/44 MAP kinase cascade both in vitro and in vivo. Taken together with previous data, our results also suggest that a novel form of reciprocal negative regulation exists between p42/44 MAP kinase activation and caveolin-1 protein expression, i.e. up-regulation of caveolin-1 protein expression down- modulates p42/44 MAP kinase activity (this report) and up-regulation of p42/44 MAP kinase activity down-regulates caveolin-1 mRNA and protein expression.
AB - The p42/44 mitogen-activated protein (MAP)-kinase cascade is a well- established signal transduction pathway that is initiated at the cell surface and terminates within the nucleus. More specifically, receptor tyrosine kinases can indirectly activate Raf, which in turn leads to activation of MEK and ERK and ultimately phosphorylation of Elk, a nuclear transcription factor. Recent reports have suggested that some members of p42/44 MAP kinase cascade can be sequestered within plasmalemmal caveolae in vivo. For example, morphological studies have directly shown that ERK-1/2 is concentrated in plasma membrane caveolae in vivo using immunoelectron microscopy. In addition, constitutive activation of the p42/44 MAP kinase cascade is sufficient to reversibly down-regulate caveolin-1 mRNA and protein expression. However, the functional relationship between the p42/44 MAP kinase cascade and caveolins remains unknown. Here, we examine the in vivo role of caveolins in regulating signaling along the MAP kinase cascade. We find that co-expression with caveolin 1 dramatically inhibits signaling from EGF-R, Raf, MEK-1 and ERK-2 to the nucleus. Using a variety of caveolin-1 deletion mutants, we mapped this in vivo inhibitory activity to caveolin-1 residues 32-95. Peptides derived from this region of caveolin 1 also inhibit the in vitro kinase activity of purified MEK-1 and ERK-2. Thus, we show here that caveolin-1 expression can inhibit signal transduction from the p42/44 MAP kinase cascade both in vitro and in vivo. Taken together with previous data, our results also suggest that a novel form of reciprocal negative regulation exists between p42/44 MAP kinase activation and caveolin-1 protein expression, i.e. up-regulation of caveolin-1 protein expression down- modulates p42/44 MAP kinase activity (this report) and up-regulation of p42/44 MAP kinase activity down-regulates caveolin-1 mRNA and protein expression.
KW - Caveolin
KW - Kinase activity
KW - Protein phosphorylation
KW - Reciprocal regulation
KW - p42/44 mitogen-activated protein kinase cascade
UR - http://www.scopus.com/inward/record.url?scp=0032577647&partnerID=8YFLogxK
U2 - 10.1016/S0014-5793(98)00470-0
DO - 10.1016/S0014-5793(98)00470-0
M3 - Article
C2 - 9654135
AN - SCOPUS:0032577647
SN - 0014-5793
VL - 428
SP - 205
EP - 211
JO - FEBS Letters
JF - FEBS Letters
IS - 3
ER -