TY - JOUR
T1 - Dp71ab/DAPs complex composition changes during the differentiation process in PC12 cells
AU - Romo-Yáñez, J.
AU - Ceja, V.
AU - Ilarraza-Lomelí, R.
AU - Coral-Vázquez, R.
AU - Velázquez, F.
AU - Mornet, D.
AU - Rendón, A.
AU - Montañez, C.
N1 - Funding Information:
B. Ilmer and A. Reijs are supported by the Dutch Heart Foundation (grant NHS 87.079). M Pozzoli is supported by Fondazione dinka del Lavoro, Centro Medico di Montescano, Pavia, Italy. A. Salustri is supported by the Interuniversity Cardiology Institute of The Netherlands (grant no. 5442).
PY - 2007/9/1
Y1 - 2007/9/1
N2 - PC12 cells express different Dp71 isoforms originated from alternative splicing; one of them, Dp71ab lacks exons 71 and 78. To gain insight into the function of Dp71 isoforms we identified dystrophin associated proteins (DAPs) that associate in vivo with Dp71 ab during nerve growth factor (NGF) induced differentiation of PC12 cells. DAPs expression was analyzed by RT-PCR, Western blot and indirect immunofluorescence, showing the presence of each mRNA and protein corresponding to α-, β-, γ-, δ-, and ε-sarcoglycans as well as ζ-sarcoglycan mRNA. Western blot analysis also revealed the expression of β-dystroglycan, α1-syntrophin, α1-, and β-dystrobrevins. We have established that Dp71ab forms a complex with β-dystroglycan, α1-syntrophin, β-dystrobrevin, and α-, β- and γ-sarcoglycans in undifferentiated PC12 cells. In differentiated PC12 cells, the complex composition changes since Dp71ab associates only with β-dystroglycan, α1 -syntrophin, β-dystrobrevin, and δ-sarcoglycan. Interestingly, neuronal nitric oxide synthase associates with the Dp71ab/DAPs complex during NGF treatment, raising the possibility that Dp71 ab may be involved in signal transduction events during neuronal differentiation.
AB - PC12 cells express different Dp71 isoforms originated from alternative splicing; one of them, Dp71ab lacks exons 71 and 78. To gain insight into the function of Dp71 isoforms we identified dystrophin associated proteins (DAPs) that associate in vivo with Dp71 ab during nerve growth factor (NGF) induced differentiation of PC12 cells. DAPs expression was analyzed by RT-PCR, Western blot and indirect immunofluorescence, showing the presence of each mRNA and protein corresponding to α-, β-, γ-, δ-, and ε-sarcoglycans as well as ζ-sarcoglycan mRNA. Western blot analysis also revealed the expression of β-dystroglycan, α1-syntrophin, α1-, and β-dystrobrevins. We have established that Dp71ab forms a complex with β-dystroglycan, α1-syntrophin, β-dystrobrevin, and α-, β- and γ-sarcoglycans in undifferentiated PC12 cells. In differentiated PC12 cells, the complex composition changes since Dp71ab associates only with β-dystroglycan, α1 -syntrophin, β-dystrobrevin, and δ-sarcoglycan. Interestingly, neuronal nitric oxide synthase associates with the Dp71ab/DAPs complex during NGF treatment, raising the possibility that Dp71 ab may be involved in signal transduction events during neuronal differentiation.
KW - Dystrophin Dp71ab
KW - Dystrophin associated proteins (DAPs)
KW - Dystrophin glycoprotein complex (DGC)
KW - NGF-induced differentiation
KW - PC12 cells
UR - http://www.scopus.com/inward/record.url?scp=34548506970&partnerID=8YFLogxK
U2 - 10.1002/jcb.21281
DO - 10.1002/jcb.21281
M3 - Artículo
C2 - 17390338
SN - 0730-2312
VL - 102
SP - 82
EP - 97
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 1
ER -