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Non-transactivational, dual pathways for LPA-induced Erk1/2 activation in primary cultures of brown pre-adipocytes

Holmström, Therese E. (författare)
Stockholms universitet,Wenner-Grens institut
Mattsson, Charlotte L. (författare)
Stockholms universitet,Wenner-Grens institut
Wang, Yanling, 1982- (författare)
Stockholms universitet,Wenner-Grens institut
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Iakovleva, Irina (författare)
Stockholms universitet,Wenner-Grens institut
Petrovic, Natasa (författare)
Stockholms universitet,Wenner-Grens institut
Nedergaard, Jan (författare)
Stockholms universitet,Wenner-Grens institut
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 (creator_code:org_t)
Elsevier BV, 2010
2010
Engelska.
Ingår i: Experimental Cell Research. - : Elsevier BV. - 0014-4827 .- 1090-2422. ; 316:16, s. 2664-75
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In many cell types, G-protein-coupled receptor (GPCR)-induced Erk1/2 MAP kinase activation is mediated via receptor tyrosine kinase (RTK) transactivation, in particular via the epidermal growth factor (EGF) receptor. Lysophosphatidic acid (LPA), acting via GPCRs, is a mitogen and MAP kinase activator in many systems, and LPA can regulate adipocyte proliferation. The mechanism by which LPA activates the Erk1/2 MAP kinase is generally accepted to be via EGF receptor transactivation. In primary cultures of brown pre-adipocytes, EGF can induce Erk1/2 activation, which is obligatory and determinant for EGF-induced proliferation of these cells. Therefore, we have here examined whether LPA, via EGF transactivation, can activate Erk1/2 in brown pre-adipocytes. We found that LPA could induce Erk1/2 activation. However, the LPA-induced Erk1/2 activation was independent of transactivation of EGF receptors (or PDGF receptors) in these cells (whereas in transformed HIB-1B brown adipocytes, the LPA-induced Erk1/2 activation indeed proceeded via EGF receptor transactivation). In the brown pre-adipocytes, LPA instead induced Erk1/2 activation via two distinct non-transactivational pathways, one G(i)-protein dependent, involving PKC and Src activation, the other, a PTX-insensitive pathway, involving PI3K (but not Akt) activation. Earlier studies showing LPA-induced Erk1/2 activation being fully dependent on RTK transactivation have all been performed in cell lines and transfected cells. The present study implies that in non-transformed systems, RTK transactivation may not be involved in the mediation of GPCR-induced Erk1/2 MAP kinase activation

Ämnesord

NATURVETENSKAP  -- Biologi -- Annan biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Other Biological Topics (hsv//eng)

Nyckelord

Lysophosphatidic acid
Transactivation
Brown adipocytes
Erk1/2
EGF receptor
PI3K
fysiologi
Physiology

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