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1000 Titel
  • Development of a Sensitive Bioassay for the Analysis of IGF-Related Activation of AKT/mTOR Signaling in Biological Matrices
1000 Autor/in
  1. Walz, Michael |
  2. Höflich, Christine |
  3. Walz, Christina |
  4. Ohde, Daniela |
  5. Brenmoehl, Julia |
  6. Sawitzky, Mandy |
  7. Vernunft, Andreas |
  8. Zettl, Uwe K. |
  9. Holtze, Susanne |
  10. Hildebrandt, Thomas B |
  11. Wolf, Eckhard |
  12. Hoeflich, Andreas |
1000 Erscheinungsjahr 2021
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-02-24
1000 Erschienen in
1000 Quellenangabe
  • 10(3):482
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3390/cells10030482 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995968/ |
1000 Ergänzendes Material
  • https://www.mdpi.com/2073-4409/10/3/482#supplementary |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The bioactivity of the IGF system is not a function of isolated hormone concentrations in a given biological matrix. Instead, the biological activities of IGFs are regulated by IGFBPs, IGFBP proteases, and inhibitors of IGFBP proteases. Therefore, assays based on IGF-related bioactivity may describe functions of the complete IGF system in a given biological matrix. Of particular interest are the IGF system effects on the AKT/mTOR pathway, as a dominant system for controlling growth, metabolism, and aging. In order to improve the sensitivity of IGF-dependent bioactivity, we made use of the known short-term and enhancing effects of IGFBP2 on the intracellular PI3K pathway. As a specific readout of this pathway, and further as a marker of the mTOR pathway, we assessed the phosphorylation of AKT-Ser473. Preincubation using IGFBP2 enhanced IGF1-dependent AKT-Ser473 phosphorylation in our experimental system. The assay’s specificity was demonstrated by inhibition of IGF1 receptors outside or inside the cell, using antiserum or small molecule inhibitors, which reduced AKT phosphorylation in response to exogenous IGF1 (p < 0.05). The maximal response of AKT phosphorylation was recorded 15 to 60 min after the addition of IGF1 to cell monolayers (p < 0.001). In our cellular system, insulin induced AKT phosphorylation only at supra-physiological concentrations (µM). Using this novel assay, we identified the differential biological activity of the IGF system in AKT-Ser473 phosphorylation in serum (mouse, naked mole rat, and human), in cerebrospinal fluid (human), and in colostrum or mature milk samples (dairy cow). We have developed a sensitive and robust bioassay to assess the IGF-related activation of the AKT/mTOR pathway. The assay works efficiently and does not require expensive cell culture systems. By using capillary immuno-electrophoresis, the readout of IGF-related bioactivity is substantially accelerated, requiring a minimum of hands-on time. Importantly, the assay system is useful for studying IGF-related activity in the AKT/mTOR pathway in a broad range of biological matrices.
1000 Sacherschließung
lokal milk
lokal bioactivity
lokal western immunoblotting
lokal bioassay
lokal capillary immuno-electrophoresis
lokal mTOR
lokal IGF
lokal colostrum
lokal BIRA assay
lokal AKT phosphorylation
lokal cerebrospinal fluid
lokal serum
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/V2FseiwgTWljaGFlbA==|https://frl.publisso.de/adhoc/uri/SMO2ZmxpY2gsIENocmlzdGluZQ==|https://frl.publisso.de/adhoc/uri/V2FseiwgQ2hyaXN0aW5h|https://orcid.org/0000-0002-0669-8409|https://orcid.org/0000-0002-7958-0655|https://frl.publisso.de/adhoc/uri/U2F3aXR6a3ksIE1hbmR5|https://frl.publisso.de/adhoc/uri/VmVybnVuZnQsIEFuZHJlYXM=|https://frl.publisso.de/adhoc/uri/WmV0dGwsIFV3ZSBLLg==|https://orcid.org/0000-0002-4654-1916|https://frl.publisso.de/adhoc/uri/SGlsZGVicmFuZHQsIFRob21hcyBC|https://frl.publisso.de/adhoc/uri/V29sZiwgRWNraGFyZA==|https://frl.publisso.de/adhoc/uri/SG9lZmxpY2gsIEFuZHJlYXM=
1000 (Academic) Editor
1000 Label
1000 Förderer
  1. H. Wilhelm Schaumann Stiftung |
  2. Leibniz-Gemeinschaft |
  3. Leibniz-Institut für Nutztierbiologie |
1000 Fördernummer
  1. -
  2. -
  3. -
1000 Förderprogramm
  1. -
  2. Open Access Fund
  3. Open Access Fund
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer H. Wilhelm Schaumann Stiftung |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Leibniz-Gemeinschaft |
    1000 Förderprogramm Open Access Fund
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Leibniz-Institut für Nutztierbiologie |
    1000 Förderprogramm Open Access Fund
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6434323.rdf
1000 Erstellt am 2022-07-27T12:28:54.198+0200
1000 Erstellt von 317
1000 beschreibt frl:6434323
1000 Bearbeitet von 317
1000 Zuletzt bearbeitet 2022-08-05T16:12:58.864+0200
1000 Objekt bearb. Fri Aug 05 16:12:58 CEST 2022
1000 Vgl. frl:6434323
1000 Oai Id
  1. oai:frl.publisso.de:frl:6434323 |
1000 Sichtbarkeit Metadaten public
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