TY - JOUR
T1 - Receptor-type protein tyrosine phosphatase ζ as a component of the signaling receptor complex for midkine-dependent survival of embryonic neurons
AU - Sakaguchi, Nahoko
AU - Muramatsu, Hisako
AU - Ichihara-Tanaka, Keiko
AU - Maeda, Nobuaki
AU - Noda, Masaharu
AU - Yamamoto, Tokuo
AU - Michikawa, Makoto
AU - Ikematsu, Shinya
AU - Sakuma, Sadatoshi
AU - Muramatsu, Takashi
N1 - Funding Information:
This work was supported by grants from the Ministry of Education, Science, Sports, Culture and Technology of Japan, Japan Society for the Promotion of Science and from CREST.
PY - 2003/2/1
Y1 - 2003/2/1
N2 - Midkine (MK), a heparin-binding growth factor, suppresses apoptosis of embryonic neurons in culture, induced by serum deprivation. Receptor-type protein tyrosine phosphatase ζ (PTP ζ) is a chondroitin sulfate proteoglycan with a transmembrane domain and intracellular tyrosine phosphatase domains. The activity of MK was abolished by digestion with chondroitinase ABC, or addition of the antibody to PTP ζ, while digestion with heparitinase showed no significant effect. These results suggested that the survival-promoting signal of MK was received by a receptor complex containing PTP ζ. Low density lipoprotein receptor-related protein (LRP) has been identified as another component of the signaling receptor. Ectodomains of two related proteins expressed on neurons, namely LRP6 and apoE receptor 2, were FLAG-tagged and examined for MK binding, using MK-agarose column. Both the ectodomains were found to exhibit calcium-dependent binding to MK. These proteins may participate in MK signaling in certain cases. The survival-promoting activity of MK was abolished by PP1, an inhibitor of src protein kinase, pertussis toxin, an inhibitor of G protein-linked signaling and sodium orthovanadate, an inhibitor of PTPs.
AB - Midkine (MK), a heparin-binding growth factor, suppresses apoptosis of embryonic neurons in culture, induced by serum deprivation. Receptor-type protein tyrosine phosphatase ζ (PTP ζ) is a chondroitin sulfate proteoglycan with a transmembrane domain and intracellular tyrosine phosphatase domains. The activity of MK was abolished by digestion with chondroitinase ABC, or addition of the antibody to PTP ζ, while digestion with heparitinase showed no significant effect. These results suggested that the survival-promoting signal of MK was received by a receptor complex containing PTP ζ. Low density lipoprotein receptor-related protein (LRP) has been identified as another component of the signaling receptor. Ectodomains of two related proteins expressed on neurons, namely LRP6 and apoE receptor 2, were FLAG-tagged and examined for MK binding, using MK-agarose column. Both the ectodomains were found to exhibit calcium-dependent binding to MK. These proteins may participate in MK signaling in certain cases. The survival-promoting activity of MK was abolished by PP1, an inhibitor of src protein kinase, pertussis toxin, an inhibitor of G protein-linked signaling and sodium orthovanadate, an inhibitor of PTPs.
KW - Apoptosis
KW - Chondroitin sulfate proteoglycan
KW - LRP6
KW - Low density lipoprotein receptor-related protein
KW - Midkine
KW - Receptor-type protein tyrosine phosphatase ζ
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U2 - 10.1016/S0168-0102(02)00226-2
DO - 10.1016/S0168-0102(02)00226-2
M3 - Article
C2 - 12573468
AN - SCOPUS:0037306398
SN - 0168-0102
VL - 45
SP - 219
EP - 224
JO - Neuroscience Research
JF - Neuroscience Research
IS - 2
ER -