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Volume 271,
Number 12,
Issue of March 22, 1996 pp. 6631-6635
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Physical and
Functional Association of Cortactin with Syk in Human Leukemic Cell
Line K562
(Received for publication, July 31, 1995; and in revised form, December 12, 1995)
Shingo
Maruyama ,
Tomohiro
Kurosaki
,
Kiyonao
Sada
,
Yuji
Yamanashi
,
Tadashi
Yamamoto
,
Hirohei
Yamamura
Human leukemic cell line K562 is induced to differentiate into
the megakaryocytic lineage by stimulation with
12-O-tetradecanoylphorbol-13-acetate (TPA). We demonstrate
here that TPA stimulation increases tyrosine phosphorylation of an
80-kDa protein at an early stage of megakaryocytic differentiation and
that this 80-kDa protein is identical with cortactin. Since tyrosine
kinase Syk was activated by TPA stimulation, we examined the
possibility that cortactin is a potential substrate of Syk in K562
cells. TPA-induced tyrosine phosphorylation of cortactin was decreased
profoundly by overexpression of dominant-negative Syk. Furthermore,
cortactin was associated with Syk even before TPA stimulation. Since
cortactin was previously referred as an 80/85-kilodalton
pp60 substrate, we examined the association
between Src and cortactin, whereas its association could not be
detected. These data suggest that Syk phosphorylates cortactin in K562
cells upon TPA treatment.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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