dc.contributor.author
Janssen, Joseph A. M. J. L.
dc.contributor.author
Hofland, Leo J.
dc.contributor.author
Strasburger, Christian J.
dc.contributor.author
Dungen, Elisabeth S. R. van den
dc.contributor.author
Thevis, Mario
dc.date.accessioned
2018-06-08T03:23:19Z
dc.date.available
2016-04-29T08:46:23.792Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15074
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19262
dc.description.abstract
Aims To compare full-length mechano growth factor (full-length MGF) with human
recombinant insulin-like growth factor-I (IGF-I) and human recombinant insulin
(HI) in their ability to activate the human IGF-I receptor (IGF-IR), the human
insulin receptor (IR-A) and the human insulin receptor-B (IR-B), respectively.
In addition, we tested the stimulatory activity of human MGF and its
stabilized analog Goldspink-MGF on the IGF-IR. Methods The effects of full-
length MGF, IGF-I, human mechano growth factor (MGF), Goldspink-MGF and HI
were compared using kinase specific receptor activation (KIRA) bioassays
specific for IGF-I, IR-A or IR-B, respectively. These assays quantify activity
by measuring auto-phosphorylation of the receptor upon ligand binding. Results
IGF-IR: At high equimolar concentrations maximal IGF-IR stimulating effects
generated by full-length MGF were similar to that of IGF-I (89-fold vs.
77-fold, respectively). However, EC50 values of IGF-I and full-length MGF for
the IGF-I receptor were 0.86 nmol/L (95% CI 0.69–1.07) and 7.83 nmol/L (95%
CI: 4.87–12.58), respectively. No IGF-IR activation was observed by human MGF
and Goldspink-MGF, respectively. IR-A/IR-B: At high equimolar concentrations
similar maximal IR-A stimulating effects were observed for full -length MGF
and HI, but maximal IR-B stimulation achieved by full -length MGF was stronger
than that by HI (292-fold vs. 98-fold). EC50 values of HI and full-length MGF
for the IR-A were 1.13 nmol/L (95% CI 0.69–1.84) and 73.11 nmol/L
(42.87–124.69), respectively; for IR-B these values were 1.28 nmol/L (95% CI
0.64–2.57) and 35.10 nmol/L (95% 17.52–70.33), respectively. Conclusions Full-
length MGF directly stimulates the IGF-IR. Despite a higher EC50
concentration, at high equimolar concentrations full-length MGF showed a
similar maximal potency to activate the IGF-IR as compared to IGF-I. Further
research is needed to understand the actions of full-length MGF in vivo and to
define the physiological relevance of our in vitro findings.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Potency of Full- Length MGF to Induce Maximal Activation of the IGF-I R Is
Similar to Recombinant Human IGF-I at High Equimolar Concentrations
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
PLoS ONE. - 11 (2016), 3, Artikel Nr. e0150453
dcterms.bibliographicCitation.doi
10.1371/journal.pone.0150453
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1371/journal.pone.0150453
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000024453
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000006352
dcterms.accessRights.openaire
open access