Summary

В режиме реального времени Визуализация лейкотриена B 4 Опосредованного миграции клеток и BLT1 Взаимодействие с β-arrestin

Published: December 23, 2010
doi:

Summary

Эта статья описывает методологию для определения хемотаксиса лейкоцитов ответ на специфических лигандов и определить взаимодействие между рецепторами клеточной поверхности и цитозольного белков с использованием живых методов визуализации клеток.

Abstract

G-protein coupled receptors (GPCRs) belong to the seven transmembrane protein family and mediate the transduction of extracellular signals to intracellular responses. GPCRs control diverse biological functions such as chemotaxis, intracellular calcium release, gene regulation in a ligand dependent manner via heterotrimeric G-proteins1-2. Ligand binding induces a series of conformational changes leading to activation of heterotrimeric G-proteins that modulate levels of second messengers such as cyclic adenosine monophosphate (cAMP), inositol triphosphate (IP3) and diacyl glycerol (DG). Concomitant with activation of the receptor ligand binding also initiates a series of events to attenuate the receptor signaling via desensitization, sequestration and/or internalization. The desensitization process of GPCRs occurs via receptor phosphorylation by G-protein receptor kinases (GRKs) and subsequent binding of β-arrestins3. β-arrestins are cytosolic proteins and translocate to membrane upon GPCR activation, binding to phosphorylated receptors (most cases) there by facilitating receptor internalization 4-6.

Leukotriene B4 (LTB4) is a pro-inflammatory lipid molecule derived from arachidonic acid pathway and mediates its actions via GPCRs, LTB4 receptor 1 (BLT1; a high affinity receptor) and LTB4 receptor 2 (BLT2; a low affinity receptor)7-9. The LTB4-BLT1 pathway has been shown to be critical in several inflammatory diseases including, asthma, arthritis and atherosclerosis10-17. The current paper describes the methodologies developed to monitor LTB4-induced leukocyte migration and the interactions of BLT1 with β-arrestin and , receptor translocation in live cells using microscopy imaging techniques18-19.

Bone marrow derived dendritic cells from C57BL/6 mice were isolated and cultured as previously described 20-21. These cells were tested in live cell imaging methods to demonstrate LTB4 induced cell migration. The human BLT1 was tagged with red fluorescent protein (BLT1-RFP) at C-terminus and β-arrestin1 tagged with green fluorescent protein (β-arr-GFP) and transfected the both plasmids into Rat Basophilic Leukomia (RBL-2H3) cell lines18-19. The kinetics of interaction between these proteins and localization were monitored using live cell video microscopy. The methodologies in the current paper describe the use of microscopic techniques to investigate the functional responses of G-protein coupled receptors in live cells. The current paper also describes the use of Metamorph software to quantify the fluorescence intensities to determine the kinetics of receptor and cytosolic protein interactions.

Protocol

Методология Описание микроскоп Живая клетка экспериментов изображений производится с помощью FM-TE-эпи-флуоресценции систему, подключенную к инвертированный микроскоп Nikon Eclipse, TE300. Микроскоп оснащен отопления стадии. Прохладный оснастки HQ цифрового Ч / Б CCD (…

Discussion

Живая клетка изображений является мощным инструментом для демонстрации функции и взаимодействие специфических белков, как они происходят в режиме реального времени. Методы, описанные в этой рукописи ясно показывают, что LTB 4 может вызвать быструю миграцию дендритных клеток. Эти …

Disclosures

The authors have nothing to disclose.

Acknowledgements

Исследование поддержано Национальным институтом здоровья гранты АИ-52 381, CA138623 и Кентукки рака легких совета исследований и организационной поддержке со Джеймс Грэм Браун онкологический центр.

Materials

Material Name Type Company Catalogue Number Comment
Cell lines:        
Rat Basophilic Leukomia Cell line (RBL-2H3) or HEK293 cells.   ATCC CRL-2256  
Media:        
Delbecco’s modified Eagle’s Medium (DMEM)   Invitrogen 11995  
Phenol red free RPMI or DMEM   Invitrogen 11835-030  
Fetal Bovine Serum   Invitrogen 16000-044  
L-Glutamine (200 mM)   Invitrogen 25030  
Penicillin-streptomycin (10000 U/mL)   Invitrogen 15140  
Trypsin, 0.05% (1X) with EDTA 4Na, liquid   Invitrogen 25300  
HEPES (1M)   Invitrogen 15630  
Others:        
35 mm sterile glass coverslip-bottomed Fluoro dishes (0.17 mm thick) (WillCo-dish)   WPI FD35-100  
Sterile Gene Pulser Cuvette (0.4 cm electrode gap) (Bio-Rad)   Bio-Rad 16552088  
Instruments/software:        
Gene Pulser II electroporater   Bio-Rad    
TE-FM Epi-Fluorescence system attached to Nikon Inverted Microscope Eclipse TE300   Nikon    
Metamorph Software   Universal Imaging    
Vertical Micro-pipette puller   Narishige International    
Micro-Forge M-900   Narishige International    
Hadraulic Micromanipulator MO-188NE   Narishige International    
Coarse Manual Manipulator, MN-188NE   Narishige International    
cDNA constructs:        
cDNA of G-Protein coupled receptor tagged with red fluorescence protein at C-terminus (hBLT1-RFP)   Jala et al 2005    
cDNA of cytosolic protein tagged with GFP (β-arrestin1-GFP in present study).   Jala et al 2005    

References

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Cite This Article
Jala, V. R., Haribabu, B. Real-time Imaging of Leukotriene B4 Mediated Cell Migration and BLT1 Interactions with β-arrestin. J. Vis. Exp. (46), e2315, doi:10.3791/2315 (2010).

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