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In This Article

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

Summary

The present protocol describes lipid supplementation methods in liquid and on-plate cultures for Caenorhabditis elegans, coupled with longitudinal studies and gene transcriptional analysis from bulk or a few worms and worm tissues.

Abstract

Aging is a complex process characterized by progressive physiological changes resulting from both environmental and genetic contributions. Lipids are crucial in constituting structural components of cell membranes, storing energy, and as signaling molecules. Regulation of lipid metabolism and signaling is essential to activate distinct longevity pathways. The roundworm Caenorhabditis elegans is an excellent and powerful organism to dissect the contribution of lipid metabolism and signaling in longevity regulation. Multiple research studies have described how diet supplementation of specific lipid molecules can extend C. elegans lifespan; however, minor differences in the supplementation conditions can cause reproducibility issues among scientists in different labs. Here, two detailed supplementation methods for C. elegans are reported employing lipid supplementation either with bacteria seeded on plates or bacterial suspension in liquid culture. Also provided herein are the details to perform lifespan assays with lifelong lipid supplementation and qRT-PCR analysis using a whole worm lysate or dissected tissues derived from a few worms. Using a combination of longitudinal studies and transcriptional investigations upon lipid supplementation, the feeding assays provide dependable approaches to dissect how lipids influence longevity and healthy aging. This methodology can also be adapted for various nutritional screening approaches to assess changes in a subset of transcripts using either a small number of dissected tissues or a few animals.

Introduction

Lipids
Lipids are small hydrophobic or amphipathic molecules soluble in organic solvents but insoluble in water1,2. Distinct lipid molecules differentiate from each other based on the number of carbons contained in their chains, location, number of double bonds, and bound structures, including glycerol or phosphates. Lipids play crucial roles within and across distinct cells to regulate organismal functions, including constituting membrane bilayers, providing energy storage, and acting as signaling molecules3,4.

Protocol

Figure 1 depicts a schematic of lipid feeding using different experimental settings.

1. Preparation of lipid-conditioned bacteria

  1. Prepare the Bacterial dilution dietary restriction (BDR) base solution by dissolving 5.85 g of NaCl, 1.0 g of K2HPO4, and 6.0 g of KH2PO4 (see Table of Materials) in 999 mL of deionized water. Adjust the pH to 6.0 with 0.5 M KOH, and then filter th.......

Representative Results

Validation of transcriptional changes using a few whole worms upon lipid supplementation
To investigate whether the protocol to extract and retrotranscribe RNA into cDNA from a few whole worms is reproducible and comparable with the data from bulk worms, a long-lived worm strain overexpressing the lysosomal acid lipase lipl-4 in the intestine was employed7,8,33,35

Discussion

Lipid supplementation has been employed in aging research to elucidate the direct impact of certain lipid species on healthy aging6,7,23,26,27,31. However, the lipid supplementation procedure can be challenging, and any inconsistency between experiments can cause non-reproducible results. Here, the first detailed step-by-step.......

Acknowledgements

We thank P. Svay for maintenance support. This work was supported by NIH grants R01AG045183 (MCW), R01AT009050 (MCW), R01AG062257 (MCW), DP1DK113644 (MCW), March of Dimes Foundation (MCW), Welch Foundation (MCW), HHMI investigator (M.C.W.), and NIH T32 ES027801 pre-doctoral student fellow (M.S.). Some strains were provided by the CGC, which is funded by the NIH Office of Research Infrastructure Programs (P40 OD010440).

....

Materials

NameCompanyCatalog NumberComments
1.5 mL PestleGenesee Scientific93-165P15For worm grinding with Trizol
AgaroseSigmaA9639-500G
AmfiRivert cDNA Synthesis Platinum Master MixGenDEPOTR5600For reverse transcription from bulk worm samples
Applied Biosystems QuanStudio 3 Real-Time PCRThermoFisherA28567For qRT-PCR
Benchmark Scientific StripSpin 12 MicrocentrifugeBenchmark ScientificC1248For spin down PCR tubes
Branson 450 Digital Sonifier, w/ 1/8" tipBranson Ultrasonic Corporation100-132-888R
ChloroformFisher ScientificC298-500
CholesterolSigmaC8503-25G
Dimethyl sulfoxide (DMSO)SigmaD8418-100ML
Eppendorf 5424 R centrifugeEppendorf22620444RFor RNA extraction
Eppendorf vapo protect mastercycler proEppendorf950030010For reverse transcription
Ethanol, Absolute (200 Proof)Fisher ScientificBP2818-500
Greiner Bio-One CELLSTAR, 12 W PlateNeta Scientific66518012-well plates for licuid feeding
Greiner Bio-One Petri Dish, Ps, 100 x 20 mmNeta Scientific664161For bacterial LB plates and worm 10-cm NGM plates
Greiner Bio-One Petri Dish, Ps, 60 x 15 mmNeta Scientific628161For worm6-cm NGM plates
Invitrogen nuclease-free waterThermoFisherAM9937
IsoproanolSigmaPX1835-2
Levamisole hydrochlorideVWRSPCML1054
lipl-4TgMCW LabN/ATransgenic C. elegans
lipl-4Tg;fat-3(wa22)MCW LabN/ATransgenic C. elegans
Luria Broth BaseThermoFisher12795-084
Magnesium sulfate (MgSO4)SigmaM2643-500G
MicroAmp EnduraPlate Optical 96-Well Fast Clear Reaction Plate with BarcodeThermoFisher448335496-well qPCR plate
MicroAmp Optical Adhesive FilmApplied BioSystem4311971For sealing the 96-well qPCR plate
Milli-Q Advantage A10 Water Purification SystemSigmaZ00Q0V0WWDeionized water used to make all reagents, including buffer and cultural media, unless specified as nuclease-free water in the protocol
N2Caenorhabditis Genetics CenterN/AC. elegans wild isolate
NanoDrop ND-1000 SpectrophotometerThermoFisherN/AFor measuring RNA concentration
OP50Caenorhabditis Genetics CenterN/ABacteria used as C. elegans food
Potasium phosphate dibasic trihydrate (K2HPO4·3H2O)SigmaP5504-1KG
Potasium phosphate monobasic (KH2PO4)SigmaP0662-2.5KG
Power SYBR Green cells-to-Ct kitThermoFisher4402953For reverse transcription and qPCR from a few worms or worm tissue
Power SYBR Green Master MixThermoFisher4367659For qPCR from bulk worm samples
Pure Bright germicidal ultra bleach KIK International LLC.596472101436% house bleach For worm egg preparation
Pyrex spot plate with nine depressionsSigmaCLS722085-18EAWatch glass for dissecting the worms
RNaseZap RNase Decontamination SolutionThermoFisherAM9780
Sodium cloride (NaCl)SigmaS7653-1KG
Sodium hydroxide (NaOH)SigmaSX0590-3
Sodium phosphate dibasic heptahydrate (Na2HPO4·7H2O)SigmaS9390-1KG
Thermo Sorvall Legend Mach 1.6R CentrifugeThermo7500-4337For bacteria collection
Thermo Sorvall ST 8 centrifugeThermo7500-7200For worm egg preparation
TRIzol ReagentTheroFisher15596018RNA extraction reagent
Turbo DNA-free kitThermoFisherAM1907For removing DNA contamination in RNA extractions
Vortexer 59Denville Scientific INVS7030
VWR Disposable Pellet Mixers and Cordless MotorVWR47747-370For worm grinding with Trizol
VWR Kinetic Energy 26 Joules Mini Centrifuge C1413 V-115VWRN/AFor worm collection. Discontinued model, a similar one available at VWR with Cat# 76269-064
Worm pickerWormStuff59-AWP

References

  1. Fahy, E., et al. Update of the LIPID MAPS comprehensive classification system for lipids 1. Journal of Lipid Research. 50, 9-14 (2009).
  2. Liebisch, G., et al. Update on LIPID ....

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