GFAP isoforms control intermediate filament network dynamics, cell morphology, and focal adhesions.

M Moeton, Oscar Stassen, JA Sluijs, van der Meer VWN, LJ Kluivers, van Hoorn H, T Schmidt, Reits EAJ, van Strien ME, EM Hol

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

20 Citeringar (Scopus)

Sammanfattning

Glial fibrillary acidic protein (GFAP) is the characteristic intermediate filament (IF) protein in astrocytes. Expression of its main isoforms, GFAPα and GFAPδ, varies in astrocytes and astrocytoma implying a potential regulatory role in astrocyte physiology and pathology. An IF-network is a dynamic structure and has been functionally linked to cell motility, proliferation, and morphology. There is a constant exchange of IF-proteins with the network. To study differences in the dynamic properties of GFAPα and GFAPδ, we performed fluorescence recovery after photobleaching experiments on astrocytoma cells with fluorescently tagged GFAPs. Here, we show for the first time that the exchange of GFP-GFAPδ was significantly slower than the exchange of GFP-GFAPα with the IF-network. Furthermore, a collapsed IF-network, induced by GFAPδ expression, led to a further decrease in fluorescence recovery of both GFP-GFAPα and GFP-GFAPδ. This altered IF-network also changed cell morphology and the focal adhesion size, but did not alter cell migration or proliferation. Our study provides further insight into the modulation of the dynamic properties and functional consequences of the IF-network composition.
OriginalspråkOdefinierat/okänt
Sidor (från-till)4101–4120
TidskriftCellular and Molecular Life Sciences
Volym73
Utgåva21
DOI
StatusPublicerad - 2016
MoE-publikationstypA1 Tidskriftsartikel-refererad

Nyckelord

  • intermediate filaments
  • FRAP
  • GFAP
  • astrocytoma

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