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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Stress Granules (SGs) are nonmembranous cytoplasmic structures that form in cells exposed to a variety of stresses. SGs contain mRNAs, RNA-binding proteins, small ribosomal subunits, translation-related factors, and various cell signaling proteins. This protocol describes a workflow that uses several experimental approaches to detect, characterize, and quantify bona fide SGs.

Abstract

Cells are often challenged by sudden environmental changes. Stress Granules (SGs), cytoplasmic ribonucleoprotein complexes that form in cells exposed to stress conditions, are implicated in various aspects of cell metabolism and survival. SGs modulate cellular signaling pathways, post-transcriptional gene expression, and stress response programs. The formation of these mRNA-containing granules is directly connected to cellular translation. SG assembly is triggered by inhibited translation initiation, and SG disassembly is promoted by translation activation or by inhibited translation elongation. This relationship is further highlighted by SG composition. Core SG components are stalled translation pre-initiation complexes, mRNA, and selected RNA-binding Proteins (RBPs). The purpose of SG assembly is to conserve cellular energy by sequestering translationally stalled housekeeping mRNAs, allowing for the enhanced translation of stress-responsive proteins. In addition to the core constituents, such as stalled translation preinitiation complexes, SGs contain a plethora of other proteins and signaling molecules. Defects in SG formation can impair cellular adaptation to stress and can thus promote cell death. SGs and similar RNA-containing granules have been linked to a number of human diseases, including neurodegenerative disorders and cancer, leading to the recent interest in classifying and defining RNA granule subtypes. This protocol describes assays to characterize and quantify mammalian SGs.

Introduction

Cells employ many mechanisms to respond to stress. Some responses occur at the post-transcriptional level and involve regulating mRNA translation and/or stability1,2. Stress-modulated mRNA translational arrest and degradation are associated with the formation of specific nonmembranous cellular foci, the most well characterized being Stress Granules (SGs)3. SGs are cytoplasmic foci that concentrate nontranslating mRNPs in translationally-arrested cells responding to stress (e.g., oxidation, heat shock, nutrient starvation, and viral infection)4. In additi....

Protocol

1. Cell Preparation

  1. Add autoclaved coverslips to 12 wells of a 24-well plate, as indicated in Figure 1A; this can be done using a sterile Pasteur pipette attached to a vacuum to pick up each coverslip. Gently tap the coverslip on the side of the well to release the suction, allowing the coverslip to fall into the well.
  2. Plate 1 x 105 U-2 OS (U2OS) osteosarcoma cells per well at a final volume of 500 µL of medium. Move the plate side to side and up and down several tim.......

Representative Results

Stress-induced foci are not necessarily SGs. SGs are classified as cytoplasmic foci that contain mRNAs, translation initiation factors, and RNA-binding proteins and are in equilibrium with active translation. The above protocol can be used as a template to characterize whether a given stress induces bona fide SGs.

SGs colocalize with other known SG markers, including both proteins and mRNA. SA and VRB induce cytoplasmic.......

Discussion

As evidenced by immunohistological studies in multiple diseases, chronic stress leads to the formation of different intracellular foci. For example, most neurodegenerative diseases are characterized by intracellular aggregates of insoluble proteins. The presence of SG-associated proteins in such aggregates is often the basis for concluding that such foci are SGs. A similar conclusion is also drawn when SG marker-positive cytoplasmic foci are observed in cells treated with new stress stimuli. This protocol provides a simp.......

Acknowledgements

We thank members of the Ivanov and Anderson labs for their helpful discussion and feedback on this manuscript. This work was supported by the National Institutes of Health [GM111700 and CA168872 to PA, NS094918 to PI], the National Science Centre in Poland [grant UMO-2012/06/M/NZ3/00054 to WS]. WS also acknowledges the Ministry of Science and Higher Education in Poland (Mobility Plus Program) and the Polish-American Fulbright Commission for their financial support of his research in the USA.

....

Materials

NameCompanyCatalog NumberComments
U-2 OSATCCATCC®HTB-96™- commonly written as "U2OS"
- culture at 37 °C under 5% CO2 in 10% FBS/DMEM
Dulbecco's Modification of Eagle's MediumCorning10-013-CV- abbreviated DMEM
- contains 4.5 g/L glucose, pyruvate, and phenol red
- supplemented with 10% FBS, 10 mM HEPES, and penicillin/steptomycin
- prewarm prior drug(s) dilution
Fetal Bovine SerumSigmaF2442-500ml- abbreviated FBS
- used to supplement media
HEPES (1 M)Thermo Fisher Scientific15630-080- used to supplement media
penicilline streptomycineSigmaP0781-100ml- used to supplement media
24 well plateCostar3524
lab tissuesKIMTECH SCIENCE34120- commonly called "kimwipes"
Coverglass for Growth Cover GlassesFisher Scientific12-545-82- autoclaved before used
- keep sterile in the tissue culture hood
Sodium (meta)arsenite ≥90%SigmaS7400-100G- commonly called sodium arsenite and abbreviated SA
- dissolution in water at 1 M concentration, then dilute to 100 µM as a working stock
VinorelbineTSZ CHEMRS055- abbreviated VRB
- dissolve in water to 10 mM
PuromycinSigmaP9620- used to assess translation level (ribopuromycylation)
- used to assess SG connection with active translation
- dilute in water to 10 mg/mL
Emetine dihydrochloride hydrateSigmaE2375- used in combination with puro to assess general translation level
- used to assess SG connection with active translation
- dilute in water to 10 mg/mL
CycloheximideSigmaC4859- abbreviated CHX
- used to assess SG connection with active translation
- dilute in water to 10 mg/mL
Phosphate Buffered SalineLonza / VWR95042-486- abbreviated PBS
- wash buffer for immunofluorescence
Paraformaldehyde reagent grade, crystallineSigmaP6148-500G- make a 4% solution in hot PBS in fume hood, stir until dissolved
- aliquots can be stored at - 20 °C for several months
- hazardous, use ventilation
- discard in special waste
Methanol, ACSBDH / VWRBDH1135-4LP- pre-chilled to -20°C before use
- discard in special waste
Normal Horse SerumThermo Fisher Scientific31874- abbreviated NHS
- dilute to 5% in PBS
- add sodium azide for storage at 4°C
- blocking solution for immunofluorescence
Ethanol, Pure, 200 Proof (100%),USP, KOPTECDecon Labs / VWR89125-188- dilute to 70% with water
Fisherbrand Superfrost Plus Microscope SlidesFisherbrand12-550-15
mouse anti G3BP1 antibody (TT-Y)Santa Cruzsc-81940- store at 4 °C
- use at 1/100 dilution
rabbit anti eIF4G antibody (H-300)Santa Cruzsc-11373- store at 4 °C
- 1/250 dilution
goat anti eIF3η (N-20) antibodySanta Cruzsc-16377- eIF3η is also known as eIF3b
- store at 4 °C
- 1/250 dilution
mouse anti puromycin 12D10 antibodyMilliporeMABE343- store at 4 °C
- 1/1000 dilution
Cy2 AffiniPure Donkey Anti-Mouse IgG (H+L)Jackson Immunoresearch715-225-150- reconstitute in water as per manufacturer’s instructions then store at 4°C
- 1/250 dilution
Cy3 AffiniPure Donkey Anti-Rabbit IgG (H+L)Jackson Immunoresearch711-165-152- reconstitute in water as per manufacturer’s instructions then store at 4°C
- 1/2500 dilution
Cy5 AffiniPure Donkey Anti-Goat IgG (H+L)Jackson Immunoresearch705-175-147- reconstitute in water as per manufacturer’s instructions then store at 4°C
- 1/250 dilution
Hoechst 33258 solutionSigma94403-1ML- incubate with secondary antibodies
-stock solution 0.5 mg/mL in dH20, protect from light
- Store at 4 °C
Cy3 StreptavidinJackson Immunoresearch016-160-084- reconstitute in water as per manufacturer’s instructions, then store at 4°C
- 1/250 dilution
oligo-(dT)40x probe biotinilatedIntegrated DNA Technologies (IDT)/- reconstitute in water to 100 ng/mL, aliquot and store at -20°C
- dilute in hybridation buffer 1/50 prior to use
- custom order
hybridation box//- make a moisture chamber with any storing slide box by adding humidified paper on the bottom
- prewarm the box prior use
20 x SSC bufferThermo fisher AmbionAM9763- dilute to 2X SSC using RNase Free water (DEPC treated)
- store at room temperature
- wash buffer for FISH
PerfectHybPlus Hybridization BufferSigmaH7033-50ml- block and probe incubation buffer for FISH
slide mounting mediahome made/- mix 5 g of “cold-soluble” poly(vinyl alcohol) in 20 ml of PBS
- mix by sonication, followed by stirring overnight at RT
- Add 5 ml of glycerol and 0.2 ml of 20 % sodium azide, and stir for 16 h at RT
- centrifugation at 20,000 g for 20 min, discard large pellet
- aliquot viscous liquid, long-term storage at -20°C, 1 week at 4°C
Parafilm "M"SigmaP7793-1EA- usually referred as "parafilm"
Poly(vinyl alcohol)SigmaP-8136-250G- reagent to make vinol
GlycerolSigmaG5516-100ML- reagent to make vinol
sodium azideFisher ScientificS2002-5G- preservative agent for blocking solution and vinol
- make a 20 % dilution in water

References

  1. Holcik, M., Sonenberg, N. Translational control in stress and apoptosis. Nat Rev Mol Cell Biol. 6 (4), 318-327 (2005).
  2. Yamasaki, S., Anderson, P. Reprogramming mRNA translation during stress. Curr Opin Cell Biol. 20....

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Cytoplasmic FociStress GranulesMammalian CellsU 2 OS CellsSodium ArseniteVinorelbineCycloheximidePuromycinImmunofluorescenceCell FixationCell Permeabilization

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