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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003479naa a2200361 4500
001oai:DiVA.org:liu-17895
003SwePub
008090424s2009 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-178952 URI
024a https://doi.org/10.1016/j.ghir.2008.06.0042 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Bäck, Karolinau Linköpings universitet,Cellbiologi,Hälsouniversitetet4 aut0 (Swepub:liu)karol97
2451 0a Changes in insulin and IGF-I receptor expression during differentiation of human preadipocytes
264 1b Elsevier BV,c 2009
338 a electronic2 rdacarrier
500 a Original Publication: Karolina Bäck and Hans Arnqvist, Changes in insulin and IGF-I receptor expression during differentiation of human preadipocytes, 2009, GROWTH HORMONE and IGF RESEARCH, (19), 2, 101-111. http://dx.doi.org/10.1016/j.ghir.2008.06.004 Copyright: Elsevier Science B.V., Amsterdam http://www.elsevier.com/
520 a Mature adipocytes originate from fibroblast-like precursor cells, preadipocytes, which differentiate to obtain the characteristics of adipocytes. Our aim was to investigate how differentiation of human preadipocytes affects the distribution of insulin receptors (IR) and IGF-I receptors (IGF-IR) and other cell characteristics. Preadipocytes were differentiated using indomethacine, dexamethasone, isobutyl-methylxantine (IBMX) and high concentration of insulin. Gene expression was quantified by real-time RT-PCT in preadipocytes (PA), differentiated preadipocytes (dPA) and mature adipocytes (mAD). The amount of expressed receptor protein was analyzed using receptor specific ELISAs and Western blot. We also studied DNA synthesis with radiolabeled thymidine incorporation and glucose accumulation with radiolabeled glucose. Differentiation of PA increased gene expression of IR but not IGF-IR, GLUT4, growth hormone receptor (GHR) and adiponectin appeared or increased. In PA and dPA only IR-A was expressed whereas also IR-B was detected in mAD. By Western blot and ELISA, IR and IGF-IR was phosphorylated by their own ligant at 1 nM and in dPA the acitivation of both receptors was stimulated by IGF-I, but not insulin, at 1 nM. Accumulation of glucose in PA was increased by insulin at 10 nM and by IGF-I at 1 nM and 10 nM. DNA synthesis was increased by insulin and IGF-I at 10 nM. In conclusion, both IR and IGF-IR are present in human preadipocytes and adipocytes. Differentiation is characterized by an increased IR/IGF-IR ratio.
653 a Insulin receptor isoforms
653 a Cell metabolism
653 a Growth factors
653 a MEDICINE
653 a MEDICIN
700a Arnqvist, Hansu Östergötlands Läns Landsting,Linköpings universitet,Cellbiologi,Hälsouniversitetet,Endokrin- och magtarmmedicinska kliniken US4 aut0 (Swepub:liu)hanar64
710a Linköpings universitetb Cellbiologi4 org
773t Growth Hormone & IGF Researchd : Elsevier BVg 19:2, s. 101-111q 19:2<101-111x 1096-6374x 1532-2238
856u https://liu.diva-portal.org/smash/get/diva2:212984/FULLTEXT01.pdfx primaryx Raw objecty fulltext:postprint
856u http://liu.diva-portal.org/smash/get/diva2:212984/FULLTEXT01
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-17895
8564 8u https://doi.org/10.1016/j.ghir.2008.06.004

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Bäck, Karolina
Arnqvist, Hans
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Linköpings universitet

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