TY - JOUR
T1 - The expression of PDGF-α but not PDGF-β receptors is suppressed in Swiss/3T3 fibroblasts over-expressing protein kinase C-α
AU - Fitzer-Attas, Cheryl
AU - Eldar, Hagit
AU - Eisenbach, Lea
AU - Livneh, Etta
N1 - Funding Information:
Ac~no~~edge~e~ts:T his work was supportedb y grantsf rom the US-Israel Binational ScienceF und @SF), Jerusalem,I srael (No. 990-00400()t o E.L.) and by grantsf rom the IsraelC ancerR esearchF und, the Scheefl oundationa ndt heN ationalI nstituteo f Health( CA 281 39) (to L.E.).
PY - 1994/4/4
Y1 - 1994/4/4
N2 - The generation and characterization of Swiss/3T3 cells which stably over-express protein kinase C (PKC)-α were previously described by us. In these cells over-expression of PKC-α reduced the expression of epidermal growth factor (EGF) receptor molecules [(1990) J. Biol. Chem. 265, 13290-13296]. Here we show that the expression of PDGF-α receptors, but not PDGF-β receptors, was specifically decreased in these cells. Not only were the levels of PDGF-α receptor mRNA transcript and protein significantly diminished in the PKC-α over-producing cells, but their ability to respond to short- and long-term growth factor signals was appropriately compromised. This was reflected in a reduced tyrosine autophosphorylation signal in response to PDGF-AA, as well as in decreased growth rates of PKC-α over-expressing cells when supplied with external PDGF-AA. A similar decrease in PDGF-α receptors was also demonstrated in parental Swiss/3T3 cells treated with phorbol esters. Our studies imply that PKC-α is involved in a cellular mechanism suppressing the expression of PDGF-α receptors in Swiss/3T3 cells. Hence, activation of PKC-α or alterations in its cellular levels may affect, in turn, the expression of a specific set of cell surface receptors and their responses to external growth factors.
AB - The generation and characterization of Swiss/3T3 cells which stably over-express protein kinase C (PKC)-α were previously described by us. In these cells over-expression of PKC-α reduced the expression of epidermal growth factor (EGF) receptor molecules [(1990) J. Biol. Chem. 265, 13290-13296]. Here we show that the expression of PDGF-α receptors, but not PDGF-β receptors, was specifically decreased in these cells. Not only were the levels of PDGF-α receptor mRNA transcript and protein significantly diminished in the PKC-α over-producing cells, but their ability to respond to short- and long-term growth factor signals was appropriately compromised. This was reflected in a reduced tyrosine autophosphorylation signal in response to PDGF-AA, as well as in decreased growth rates of PKC-α over-expressing cells when supplied with external PDGF-AA. A similar decrease in PDGF-α receptors was also demonstrated in parental Swiss/3T3 cells treated with phorbol esters. Our studies imply that PKC-α is involved in a cellular mechanism suppressing the expression of PDGF-α receptors in Swiss/3T3 cells. Hence, activation of PKC-α or alterations in its cellular levels may affect, in turn, the expression of a specific set of cell surface receptors and their responses to external growth factors.
KW - PDGF-α receptor
KW - PKC-α
KW - Receptor expression
UR - http://www.scopus.com/inward/record.url?scp=0028178537&partnerID=8YFLogxK
U2 - 10.1016/0014-5793(94)80493-1
DO - 10.1016/0014-5793(94)80493-1
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C2 - 8143871
VL - 342
SP - 165
EP - 170
JO - FEBS Letters
JF - FEBS Letters
SN - 0014-5793
IS - 2
ER -