Insulin-like growth factor II: complexity of biosynthesis and receptor binding

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Insulin-like growth factor II: complexity of biosynthesis and receptor binding. / Gammeltoft, S; Christiansen, Jan; Nielsen, F C; Verland, S.

In: Advances in Experimental Medicine and Biology, Vol. 293, 1991, p. 31-44.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Gammeltoft, S, Christiansen, J, Nielsen, FC & Verland, S 1991, 'Insulin-like growth factor II: complexity of biosynthesis and receptor binding', Advances in Experimental Medicine and Biology, vol. 293, pp. 31-44.

APA

Gammeltoft, S., Christiansen, J., Nielsen, F. C., & Verland, S. (1991). Insulin-like growth factor II: complexity of biosynthesis and receptor binding. Advances in Experimental Medicine and Biology, 293, 31-44.

Vancouver

Gammeltoft S, Christiansen J, Nielsen FC, Verland S. Insulin-like growth factor II: complexity of biosynthesis and receptor binding. Advances in Experimental Medicine and Biology. 1991;293:31-44.

Author

Gammeltoft, S ; Christiansen, Jan ; Nielsen, F C ; Verland, S. / Insulin-like growth factor II: complexity of biosynthesis and receptor binding. In: Advances in Experimental Medicine and Biology. 1991 ; Vol. 293. pp. 31-44.

Bibtex

@article{cad8a2908c9e11de8bc9000ea68e967b,
title = "Insulin-like growth factor II: complexity of biosynthesis and receptor binding",
abstract = "Insulin-like growth factor II (IGF-II) belongs to the insulin family of peptides and acts as a growth factor in many fetal tissues and tumors. The gene expression of IGF-II is initiated at three different promoters which gives rise to multiple transcripts. In a human rhabdomyosarcoma cell line IN 157 IGF-II mRNAs of 6.0-kb, 4.8-kb, and 4.2-kb are present. Fractionation of cellular extracts on sucrose gradients and Northern blot analysis showed that only the 4.8-kb mRNA was associated with polysomes, whereas the other transcripts cosedimented with monosomal particles. This suggests that only the 4.8-kb mRNA is translated to IGF-II. The cell line secretes two forms of immunoreactive and bioactive IGF-II to the medium of molecular size 10 kd and 7.5 kd which may be involved in autocrine control of cell growth. IGF-II binds to two receptors on the surface of many cell types: the IGF-I receptor and the mannose-6-phosphate (Man-6-P)/IGF-II receptor. There is consensus that the cellular effects of IGF-II are mediated by the IGF-I receptor via activation of its intrinsic tyrosine kinase. The Man-6-P/IGF-II receptor is involved in endocytosis of lysosomal enzymes and IGF-II. In selected cell types, however, Man-6-P induces cellular responses. We have studied rat brain neuronal precursor cells where Man-6-P acted as a mitogen suggesting that phosphomannosylated proteins may act as growth factors via the Man-6-P/IGF-II receptor. In conclusion, the gene expression and mechanism of action of IGF-II is very complex suggesting that its biological actions can be regulated at different levels including the transcription, translation, posttranslational processing, receptor binding and intracellular signalling.",
author = "S Gammeltoft and Jan Christiansen and Nielsen, {F C} and S Verland",
note = "Keywords: Animals; Carrier Proteins; Humans; Insulin-Like Growth Factor Binding Proteins; Insulin-Like Growth Factor II; Mannosephosphates; Protein Biosynthesis; Protein Processing, Post-Translational; Protein-Tyrosine Kinases; RNA, Messenger; Receptor, IGF Type 2; Receptors, Cell Surface",
year = "1991",
language = "English",
volume = "293",
pages = "31--44",
journal = "Advances in Experimental Medicine and Biology",
issn = "0065-2598",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Insulin-like growth factor II: complexity of biosynthesis and receptor binding

AU - Gammeltoft, S

AU - Christiansen, Jan

AU - Nielsen, F C

AU - Verland, S

N1 - Keywords: Animals; Carrier Proteins; Humans; Insulin-Like Growth Factor Binding Proteins; Insulin-Like Growth Factor II; Mannosephosphates; Protein Biosynthesis; Protein Processing, Post-Translational; Protein-Tyrosine Kinases; RNA, Messenger; Receptor, IGF Type 2; Receptors, Cell Surface

PY - 1991

Y1 - 1991

N2 - Insulin-like growth factor II (IGF-II) belongs to the insulin family of peptides and acts as a growth factor in many fetal tissues and tumors. The gene expression of IGF-II is initiated at three different promoters which gives rise to multiple transcripts. In a human rhabdomyosarcoma cell line IN 157 IGF-II mRNAs of 6.0-kb, 4.8-kb, and 4.2-kb are present. Fractionation of cellular extracts on sucrose gradients and Northern blot analysis showed that only the 4.8-kb mRNA was associated with polysomes, whereas the other transcripts cosedimented with monosomal particles. This suggests that only the 4.8-kb mRNA is translated to IGF-II. The cell line secretes two forms of immunoreactive and bioactive IGF-II to the medium of molecular size 10 kd and 7.5 kd which may be involved in autocrine control of cell growth. IGF-II binds to two receptors on the surface of many cell types: the IGF-I receptor and the mannose-6-phosphate (Man-6-P)/IGF-II receptor. There is consensus that the cellular effects of IGF-II are mediated by the IGF-I receptor via activation of its intrinsic tyrosine kinase. The Man-6-P/IGF-II receptor is involved in endocytosis of lysosomal enzymes and IGF-II. In selected cell types, however, Man-6-P induces cellular responses. We have studied rat brain neuronal precursor cells where Man-6-P acted as a mitogen suggesting that phosphomannosylated proteins may act as growth factors via the Man-6-P/IGF-II receptor. In conclusion, the gene expression and mechanism of action of IGF-II is very complex suggesting that its biological actions can be regulated at different levels including the transcription, translation, posttranslational processing, receptor binding and intracellular signalling.

AB - Insulin-like growth factor II (IGF-II) belongs to the insulin family of peptides and acts as a growth factor in many fetal tissues and tumors. The gene expression of IGF-II is initiated at three different promoters which gives rise to multiple transcripts. In a human rhabdomyosarcoma cell line IN 157 IGF-II mRNAs of 6.0-kb, 4.8-kb, and 4.2-kb are present. Fractionation of cellular extracts on sucrose gradients and Northern blot analysis showed that only the 4.8-kb mRNA was associated with polysomes, whereas the other transcripts cosedimented with monosomal particles. This suggests that only the 4.8-kb mRNA is translated to IGF-II. The cell line secretes two forms of immunoreactive and bioactive IGF-II to the medium of molecular size 10 kd and 7.5 kd which may be involved in autocrine control of cell growth. IGF-II binds to two receptors on the surface of many cell types: the IGF-I receptor and the mannose-6-phosphate (Man-6-P)/IGF-II receptor. There is consensus that the cellular effects of IGF-II are mediated by the IGF-I receptor via activation of its intrinsic tyrosine kinase. The Man-6-P/IGF-II receptor is involved in endocytosis of lysosomal enzymes and IGF-II. In selected cell types, however, Man-6-P induces cellular responses. We have studied rat brain neuronal precursor cells where Man-6-P acted as a mitogen suggesting that phosphomannosylated proteins may act as growth factors via the Man-6-P/IGF-II receptor. In conclusion, the gene expression and mechanism of action of IGF-II is very complex suggesting that its biological actions can be regulated at different levels including the transcription, translation, posttranslational processing, receptor binding and intracellular signalling.

M3 - Journal article

C2 - 1722620

VL - 293

SP - 31

EP - 44

JO - Advances in Experimental Medicine and Biology

JF - Advances in Experimental Medicine and Biology

SN - 0065-2598

ER -

ID: 13885597