PC12 cells overexpressing the insulin receptor undergo insulin-dependent neuronal differentiation (Q57270016)

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29 October 2019

title

PC12 cells overexpressing the insulin receptor undergo insulin-dependent neuronal differentiation (English)

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29 October 2019

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1

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29 October 2019

2

J Schlessinger

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29 October 2019

author name string

I Lax

series ordinal

3

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29 October 2019

language of work or name

English

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publication date

1 August 1994

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29 October 2019

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29 October 2019

volume

4

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issue

8

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29 October 2019

page(s)

702-708

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Signal transduction by receptors with tyrosine kinase activity

29 October 2019

cites work

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The effect of fibroblast growth factor on PC12 cells

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The trk family of tyrosine protein kinase receptors

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The beta-PDGF receptor induces neuronal differentiation of PC12 cells

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Growth factor signaling: where is the specificity?

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PC12 cell neuronal differentiation is associated with prolonged p21ras activity and consequent prolonged ERK activity

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Sustained activation of the mitogen-activated protein (MAP) kinase cascade may be required for differentiation of PC12 cells. Comparison of the effects of nerve growth factor and epidermal growth factor

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7 January 2021

Insulin and insulin-like growth factors stimulate deoxyribonucleic acid synthesis in PC12 pheochromocytoma cells

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7 January 2021

The cytoplasmic raf oncogene induces a neuronal phenotype in PC12 cells: a potential role for cellular raf kinases in neuronal growth factor signal transduction

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Acidic and basic fibroblast growth factors promote stable neurite outgrowth and neuronal differentiation in cultures of PC12 cells

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Overexpression of the trk tyrosine kinase rapidly accelerates nerve growth factor-induced differentiation

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Signal transduction by nerve growth factor and fibroblast growth factor in PC12 cells requires a sequence of src and ras actions

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Ras is essential for nerve growth factor- and phorbol ester-induced tyrosine phosphorylation of MAP kinases

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ras mediates nerve growth factor receptor modulation of three signal-transducing protein kinases: MAP kinase, Raf-1, and RSK

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How receptor tyrosine kinases activate Ras.

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The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signaling

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C. elegans cell-signalling gene sem-5 encodes a protein with SH2 and SH3 domains

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Association of the Shc and Grb2/Sem5 SH2-containing proteins is implicated in activation of the Ras pathway by tyrosine kinases

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The function of GRB2 in linking the insulin receptor to Ras signaling pathways

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Activation of the MAP kinase pathway by the protein kinase raf

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Activation of mitogen-activated protein kinase kinase by v-Raf in NIH 3T3 cells and in vitro

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Nuclear localization and regulation of erk- and rsk-encoded protein kinases

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The SH2 and SH3 domains of mammalian Grb2 couple the EGF receptor to the Ras activator mSos1

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Guanine-nucleotide-releasing factor hSos1 binds to Grb2 and links receptor tyrosine kinases to Ras signalling

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EGF triggers neuronal differentiation of PC12 cells that overexpress the EGF receptor

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Neuronal differentiation signals are controlled by nerve growth factor receptor/Trk binding sites for SHC and PLC gamma.

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Sarcoma viruses carrying ras oncogenes induce differentiation-associated properties in a neuronal cell line

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Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells

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High-efficiency expression/cloning of epidermal growth factor-receptor-binding proteins with Src homology 2 domains

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High-efficiency transformation of mammalian cells by plasmid DNA

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Mapping of the residues responsible for the negative cooperativity of the receptor-binding region of insulin

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Identifiers

DOI

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29 October 2019

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