TY - JOUR
T1 - Preserved phosphorylation of RET receptor protein in spinal motor neurons of patients with amyotrophic lateral sclerosis
T2 - An immunohistochemical study by a phosphorylation-specific antibody at tyrosine 1062
AU - Yamamoto, Masahiko
AU - Li, Mei
AU - Mitsuma, Norimasa
AU - Ito, Shinji
AU - Kato, Masashi
AU - Takahashi, Masahide
AU - Sobue, Gen
N1 - Funding Information:
This work was supported by a COE grant from the Ministry of Education, Science and Culture of Japan, and grants from the Ministry of Health and Welfare of Japan.
PY - 2001/8/31
Y1 - 2001/8/31
N2 - Ret oncoprotein is a functional receptor for the glial cell line-derived neurotrophic factor (GDNF) family and it is expressed in motor neurons, playing an important role in the motor neuron function. In this study, we examined the expression of the phosphorylation state of tyrosine residue 1062 (Tyr-1062) of Ret in the spinal cords of amyotrophic lateral sclerosis (ALS), using the phosphorylation state specific antibody at Tyr-1062 of Ret. The immunohistochemical study demonstrated that Tyr-1062 of Ret was phosphorylated to variable extents in the surviving motor neurons of all the ALS as well as controls studied. This is the first report that the phosphorylation of Tyr-1062 occurred in neurons with nononcogenic type of Ret. The Ret-signaling pathway by Tyr-1062 autophosphorylation is constitutively activated via the phosphatidylinositol 3-kinase and/or mitogen-activated protein kinase cascade for motoneuron survival even in the ALS motor neurons, supporting the view that GDNF is a candidate for therapeutic approach to ALS.
AB - Ret oncoprotein is a functional receptor for the glial cell line-derived neurotrophic factor (GDNF) family and it is expressed in motor neurons, playing an important role in the motor neuron function. In this study, we examined the expression of the phosphorylation state of tyrosine residue 1062 (Tyr-1062) of Ret in the spinal cords of amyotrophic lateral sclerosis (ALS), using the phosphorylation state specific antibody at Tyr-1062 of Ret. The immunohistochemical study demonstrated that Tyr-1062 of Ret was phosphorylated to variable extents in the surviving motor neurons of all the ALS as well as controls studied. This is the first report that the phosphorylation of Tyr-1062 occurred in neurons with nononcogenic type of Ret. The Ret-signaling pathway by Tyr-1062 autophosphorylation is constitutively activated via the phosphatidylinositol 3-kinase and/or mitogen-activated protein kinase cascade for motoneuron survival even in the ALS motor neurons, supporting the view that GDNF is a candidate for therapeutic approach to ALS.
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U2 - 10.1016/S0006-8993(01)02542-2
DO - 10.1016/S0006-8993(01)02542-2
M3 - Article
C2 - 11520496
AN - SCOPUS:0035979832
SN - 0006-8993
VL - 912
SP - 89
EP - 94
JO - Brain Research
JF - Brain Research
IS - 1
ER -