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Analysis of Phosphatidylinositol Transfer at ER-PM Junctions in Receptor-Stimulated Live Cells.
Chang, Chi-Lun; Liou, Jen.
Afiliação
  • Chang CL; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA. changc10@janelia.hhmi.org.
  • Liou J; Department of Physiology, UT Southwestern Medical Center, Dallas, TX, USA. Jen.Liou@UTSouthwestern.edu.
Methods Mol Biol ; 1949: 1-11, 2019.
Article em En | MEDLINE | ID: mdl-30790244
Phosphatidylinositol (PI) is an inositol-containing phospholipid synthesized in the endoplasmic reticulum (ER). PI is a precursor lipid for PI 4,5-bisphosphate (PI(4,5)P2) in the plasma membrane (PM) important for Ca2+ signaling in response to extracellular stimuli. Thus, ER-to-PM PI transfer becomes essential for cells to maintain PI(4,5)P2 homeostasis during receptor stimulation. In this chapter, we discuss two live-cell imaging protocols to analyze ER-to-PM PI transfer at ER-PM junctions, where the two membrane compartments make close appositions accommodating PI transfer. First, we describe how to monitor PI(4,5)P2 replenishment following receptor stimulation, as a readout of PI transfer, using a PI(4,5)P2 biosensor and total internal reflection fluorescence microscopy. The second protocol directly visualizes PI transfer proteins that accumulate at ER-PM junctions and mediate PI(4,5)P2 replenishment with PI in the ER in stimulated cells. These methods provide spatial and temporal analysis of ER-to-PM PI transfer during receptor stimulation and can be adapted to other research questions related to this topic.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositóis / Membrana Celular / Retículo Endoplasmático Limite: Humans Idioma: En Revista: Methods Mol Biol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositóis / Membrana Celular / Retículo Endoplasmático Limite: Humans Idioma: En Revista: Methods Mol Biol Ano de publicação: 2019 Tipo de documento: Article