#METABOLOMICS WORKBENCH hatalbott2_20191118_161906 DATATRACK_ID:1852 STUDY_ID:ST001286 ANALYSIS_ID:AN002137 PROJECT_ID:PR000868 VERSION 1 CREATED_ON December 12, 2019, 5:08 pm #PROJECT PR:PROJECT_TITLE Lipid composition of isolated lipid droplets from the functional bovine corpus PR:PROJECT_TITLE luteum PR:PROJECT_TYPE lipidomics PR:PROJECT_SUMMARY Establishment and maintenance of pregnancy is dependent on progesterone PR:PROJECT_SUMMARY synthesized by the corpus luteum (CL). The CL is known for the prominent PR:PROJECT_SUMMARY presence of intracellular lipid droplets (LDs). However relatively little is PR:PROJECT_SUMMARY known about the composition and function of these luteal LDs. Our objective was PR:PROJECT_SUMMARY to identify the lipid composition of LDs from fully functional bovine CLs. PR:PROJECT_SUMMARY Luteal LDs were isolated by flotation through a discontinuous sucrose gradient, PR:PROJECT_SUMMARY lipids were then extracted using a standard Bligh and Dyer protocol, dried, and PR:PROJECT_SUMMARY sent to Avanti Polar Lipids for lipidomics analysis. The samples were provided PR:PROJECT_SUMMARY for lipidomic profiling of free sterols, cholesteryl esters, triglycerides, PR:PROJECT_SUMMARY diacylglycerols, phospholipids, and sphingolipids. Molecular species were PR:PROJECT_SUMMARY resolved by reversed-phase liquid chromatography in the presence of class and PR:PROJECT_SUMMARY sub-class specific internal standard compounds added to each sample. The PR:PROJECT_SUMMARY compounds were detected by tandem mass spectrometry (MS/MS) with scheduled PR:PROJECT_SUMMARY multiple reaction monitoring (MRM) for mass-specific fragment ions according to PR:PROJECT_SUMMARY the lipid class and molecular weight of the compound. Quantification of PR:PROJECT_SUMMARY cholesterol, cholesteryl esters, triglycerides, and diglycerides were directly PR:PROJECT_SUMMARY calculated with standards and internal standards from calibration response PR:PROJECT_SUMMARY curves. The remaining lipid species were semi-quantization using the integrated PR:PROJECT_SUMMARY area of each analyte’s MRM peak, divided by the appropriate internal standard PR:PROJECT_SUMMARY peak area, and multiplied by the standard’s known concentration. Lipid PR:PROJECT_SUMMARY concentrations were normalized to the corresponding protein concentration of PR:PROJECT_SUMMARY each sample and as a mol % relative to total lipids or within each lipid class. PR:PROJECT_SUMMARY Isolated luteal LDs were composed primarily of triglyceride (88%, mol% of lipid PR:PROJECT_SUMMARY class to total lipids). Other neutral lipids included diacylglycerol, 2.9%; and PR:PROJECT_SUMMARY cholesteryl esters, 1.5%. Polar lipids were primarily composed of PR:PROJECT_SUMMARY phosphatidylcholine (3.1%), sphingomyelin (1.5%), phosphatidylinositol (0.9%), PR:PROJECT_SUMMARY phosphatidylethanolamine (0.8%) and phosphatidylserine (0.4%). A number of other PR:PROJECT_SUMMARY minor lipids representing less than 0.32% of the total lipid pool were also PR:PROJECT_SUMMARY detected including phosphatidylglycerol, lysophospholipids, ceramides, and PR:PROJECT_SUMMARY glycosylated ceramides. Lipid composition of bovine luteal LDs are distinct from PR:PROJECT_SUMMARY LDs isolated from other tissues and in other species. PR:INSTITUTE University of Nebraska Medical Center PR:DEPARTMENT Obstetrics and Gynecology PR:LABORATORY John S. Davis PR:LAST_NAME Davis PR:FIRST_NAME John PR:ADDRESS 983255 Nebraska Medical Center Omaha, NE 68198-3255 PR:EMAIL jsdavis@unmc.edu PR:PHONE 402-599-9079 PR:FUNDING_SOURCE INBRE - P20GM103427-14, COBRE - 1P30GM110768-01 PR:CONTRIBUTORS Heather Talbott, Xiaoying Hou, Crystal Cordes #STUDY ST:STUDY_TITLE Lipid composition of isolated lipid droplets from the functional bovine corpus ST:STUDY_TITLE luteum ST:STUDY_TYPE Lipidomics ST:STUDY_SUMMARY Establishment and maintenance of pregnancy is dependent on progesterone ST:STUDY_SUMMARY synthesized by the corpus luteum (CL). The CL is known for the prominent ST:STUDY_SUMMARY presence of intracellular lipid droplets (LDs). However relatively little is ST:STUDY_SUMMARY known about the composition and function of these luteal LDs. Our objective was ST:STUDY_SUMMARY to identify the lipid composition of LDs from fully functional bovine CLs. ST:STUDY_SUMMARY Luteal LDs were isolated by flotation through a discontinuous sucrose gradient, ST:STUDY_SUMMARY lipids were then extracted using a standard Bligh and Dyer protocol, dried, and ST:STUDY_SUMMARY sent to Avanti Polar Lipids for lipidomics analysis. The samples were provided ST:STUDY_SUMMARY for lipidomic profiling of free sterols, cholesteryl esters, triglycerides, ST:STUDY_SUMMARY diacylglycerols, phospholipids, and sphingolipids. Molecular species were ST:STUDY_SUMMARY resolved by reversed-phase liquid chromatography in the presence of class and ST:STUDY_SUMMARY sub-class specific internal standard compounds added to each sample. The ST:STUDY_SUMMARY compounds were detected by tandem mass spectrometry (MS/MS) with scheduled ST:STUDY_SUMMARY multiple reaction monitoring (MRM) for mass-specific fragment ions according to ST:STUDY_SUMMARY the lipid class and molecular weight of the compound. Quantification of ST:STUDY_SUMMARY cholesterol, cholesteryl esters, triglycerides, and diglycerides were directly ST:STUDY_SUMMARY calculated with standards and internal standards from calibration response ST:STUDY_SUMMARY curves. The remaining lipid species were semi-quantization using the integrated ST:STUDY_SUMMARY area of each analyte’s MRM peak, divided by the appropriate internal standard ST:STUDY_SUMMARY peak area, and multiplied by the standard’s known concentration. Lipid ST:STUDY_SUMMARY concentrations were normalized to the corresponding protein concentration of ST:STUDY_SUMMARY each sample and as a mol % relative to total lipids or within each lipid class. ST:STUDY_SUMMARY Isolated luteal LDs were composed primarily of triglyceride (88%, mol% of lipid ST:STUDY_SUMMARY class to total lipids). Other neutral lipids included diacylglycerol, 2.9%; and ST:STUDY_SUMMARY cholesteryl esters, 1.5%. Polar lipids were primarily composed of ST:STUDY_SUMMARY phosphatidylcholine (3.1%), sphingomyelin (1.5%), phosphatidylinositol (0.9%), ST:STUDY_SUMMARY phosphatidylethanolamine (0.8%) and phosphatidylserine (0.4%). A number of other ST:STUDY_SUMMARY minor lipids representing less than 0.32% of the total lipid pool were also ST:STUDY_SUMMARY detected including phosphatidylglycerol, lysophospholipids, ceramides, and ST:STUDY_SUMMARY glycosylated ceramides. Lipid composition of bovine luteal LDs are distinct from ST:STUDY_SUMMARY LDs isolated from other tissues and in other species. ST:INSTITUTE University of Nebraska Medical Center ST:DEPARTMENT Obstetrics and Gynecology ST:LABORATORY John S. Davis ST:LAST_NAME Davis ST:FIRST_NAME John ST:ADDRESS 983255 Nebraska Medical Center Omaha, NE 68198-3255 ST:EMAIL jsdavis@unmc.edu ST:PHONE 402-559-9079 ST:NUM_GROUPS 1 ST:TOTAL_SUBJECTS 3 ST:NUM_FEMALES 3 #SUBJECT SU:SUBJECT_TYPE Mammal SU:SUBJECT_SPECIES Bos taurus SU:TAXONOMY_ID 9913 SU:GENDER Female SU:ANIMAL_ANIMAL_SUPPLIER JBS Beef Plant 3435 Edward Babe Gomez Ave, Omaha, NE 68107 #SUBJECT_SAMPLE_FACTORS: SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data SUBJECT_SAMPLE_FACTORS - bovine_CL_LD_replicate1 Treatment:Control SUBJECT_SAMPLE_FACTORS - bovine_CL_LD_replicate2 Treatment:Control SUBJECT_SAMPLE_FACTORS - bovine_CL_LD_replicate3 Treatment:Control #COLLECTION CO:COLLECTION_SUMMARY Tissue (~2.5 g) was washed thoroughly in TE buffer (10 mM Tris, 1 mM EDTA, pH CO:COLLECTION_SUMMARY 7.4). Minced tissue was resuspended in 10 mL tissue homogenate buffer (60% CO:COLLECTION_SUMMARY sucrose w/v in TE buffer containing protease and phosphatase inhibitor CO:COLLECTION_SUMMARY cocktails) and homogenized with a Teflon Dounce homogenizer in a glass vessel. CO:COLLECTION_SUMMARY The post-nuclear supernatant (PNS) fraction was obtained after centrifugation at CO:COLLECTION_SUMMARY 2000 rcf for 10 min. The supernatant was loaded into a 30 mL ultracentrifuge CO:COLLECTION_SUMMARY tube and overlaid sequentially with 40%, 25%, 10%, and 0% sucrose w/v in TE CO:COLLECTION_SUMMARY buffer containing protease and phosphatase inhibitor cocktails. Samples were CO:COLLECTION_SUMMARY centrifuged at 110,000 × g (ravg) for 30 min at 4 °C with no brake in a CO:COLLECTION_SUMMARY Beckman Coulter Avanti J-20 XP ultracentrifuge using an SW 32 Ti rotor. The LDs CO:COLLECTION_SUMMARY concentrated in a yellow-ish band at the top of the gradient were harvested and CO:COLLECTION_SUMMARY concentrated by centrifugation at 2000 rcf for 10 min at 4 °C. This protocol CO:COLLECTION_SUMMARY was derived from Ding et al. 2012, and Brasaemale et al. 2016. Ding, Y., Zhang, CO:COLLECTION_SUMMARY S., Yang, L., Na, H., Zhang, P., Zhang, H., … Liu, P. (2013). Isolating lipid CO:COLLECTION_SUMMARY droplets from multiple species. Nature Protocols, 8(1), 43–51. CO:COLLECTION_SUMMARY https://doi.org/10.1038/nprot.2012.142 Brasaemle, D. L., & Wolins, N. E. (2016). CO:COLLECTION_SUMMARY Isolation of Lipid Droplets from Cells by Density Gradient Centrifugation. CO:COLLECTION_SUMMARY Current Protocols in Cell Biology, 72, 3.15.1-3.15.13. CO:COLLECTION_SUMMARY https://doi.org/10.1002/cpcb.10 CO:SAMPLE_TYPE Ovary CO:VOLUMEORAMOUNT_COLLECTED 2.5 g of corpus luteum tissue #TREATMENT TR:TREATMENT_SUMMARY N/A #SAMPLEPREP SP:SAMPLEPREP_SUMMARY Lipids from CL tissue LDs (~250uL) were extracted using a standard Bligh and SP:SAMPLEPREP_SUMMARY Dyer extraction protocol and then dried and sent to Avanti Polar Lipids for SP:SAMPLEPREP_SUMMARY lipidomics analysis. Extracts were received as dried residues in glass vials and SP:SAMPLEPREP_SUMMARY were immediately stored at -80 °C until analysis. Bligh, E. G., & Dyer, W. J. SP:SAMPLEPREP_SUMMARY (1959). A rapid method of total lipid extraction and purification. Canadian SP:SAMPLEPREP_SUMMARY Journal of Biochemistry and Physiology, 37(8), 911–917. SP:SAMPLEPREP_SUMMARY https://doi.org/10.1139/o59-099 SP:PROCESSING_STORAGE_CONDITIONS -80℃ SP:EXTRACTION_METHOD Bligh & Dyer, chloroform:methanol (1:2, v:v) SP:EXTRACT_STORAGE -80℃ SP:SAMPLE_RESUSPENSION 1mL of chloroform:methanol (8:2, v/v) SP:SAMPLE_DERIVATIZATION N/A SP:SUBCELLULAR_LOCATION Lipid Droplet #CHROMATOGRAPHY CH:CHROMATOGRAPHY_SUMMARY Molecular species were resolved by reversed-phase liquid chromatography in the CH:CHROMATOGRAPHY_SUMMARY presence of class and sub-class specific internal standard compounds added to CH:CHROMATOGRAPHY_SUMMARY each sample. Selectivity was further enhanced by scheduling the detection of CH:CHROMATOGRAPHY_SUMMARY each compound according to its elution from the high-performance liquid CH:CHROMATOGRAPHY_SUMMARY chromatography (HPLC) column, known as scheduled MRM (sMRM). CH:CHROMATOGRAPHY_TYPE Reversed phase CH:INSTRUMENT_NAME Waters Acquity CH:COLUMN_NAME Thermo Hypersil Gold C18 (50 x 1.2mm, 1.7um) CH:INTERNAL_STANDARD C17 Sphingosine, C17 Sphinganine,Cer(d18:1/12:0), GlcCer(d18:1/12:0), CH:INTERNAL_STANDARD LacCer(d18:1/12:0) #ANALYSIS AN:ANALYSIS_TYPE MS AN:LABORATORY_NAME Avanti Polar Lipids, Inc AN:DETECTOR_TYPE AcQuRate™ Pulse Counting CEM #MS MS:INSTRUMENT_NAME ABI Sciex 5500 QTrap MS:INSTRUMENT_TYPE Triple quadrupole MS:MS_TYPE ESI MS:ION_MODE POSITIVE MS:MS_COMMENTS sMRM Prec SB frag. #MS_METABOLITE_DATA MS_METABOLITE_DATA:UNITS nM MS_METABOLITE_DATA_START Samples bovine_CL_LD_replicate1 bovine_CL_LD_replicate2 bovine_CL_LD_replicate3 Factors Treatment:Control Treatment:Control Treatment:Control Sphinganine 0 0.074681748 1.109685348 Sphingosine 0 0 0 Cer(d16:1/16:0) 0.26782155 0.148291093 1.024119322 Cer(d16:1/18:0) 0.021927297 0 0.080448647 Cer(d18:1/14:0) 0.650610018 0.363639816 0.819638896 Cer(d18:2/16:0) 0.110654794 0.044851071 1.152945852 Cer(d18:1/16:1) 0 0 0 Cer(d18:1/16:0) 9.071798528 4.592071974 54.02023884 Cer(d18:1/16:0(OH)) 2.536959068 0.745097368 1.60959888 Cer(d18:2/18:1) 0.138269196 0.040078403 0.072016877 Cer(d18:1/18:1) 0.529923136 0.390715591 1.301201072 Cer(d18:1/18:0) 0 0 2.501062395 Cer(d18:2/20:1) 0.039979172 0 0.068108833 Cer(d18:2/20:0) 0.065744525 0.004268173 0 Cer(d18:1/20:0) 0 0 0 Cer(d18:2/22:1) 0.129448482 0.019610636 0.051162394 Cer(d18:1/24:1) 14.22200206 8.710743037 77.6661647 Cer(d18:1/24:0) 0 0 44.69866029 Cer(d18:1/25:0) 0 0 0 GlcCer(d18:1/14:0) 0.06555451 0.045076006 0.111433906 Cer(d18:1/26:1) 0 0 0 Cer(d18:1/26:0) 0 0 0 GlcCer(d18:1/16:1) 0 0 0 GlcCer(d18:1/16:0) 1.54852109 1.197628402 6.48766492 GlcCer(d18:1/18:1) 0 0.000516084 0.119684473 GlcCer(d18:1/18:0) 0.429260822 0.126260802 0.900671088 GlcCer(d18:1/20:1) 0 0 0.039419013 GlcCer(d18:1/20:0) 0 0.086107755 0.243094757 GlcCer(d18:1/22:0) 0.627280885 0.744028618 3.518740946 GlcCer(d18:1/24:1) 0.209399747 0.251806011 2.295401581 GlcCer(d18:1/24:0) 0.518468154 0.755765793 3.918735835 GlcCer(d18:1/26:1) 0 0 0 GlcCer(d18:1/26:0) 0 0 0 LacCer(d18:1/16:0) 1.045194528 0.306367937 2.59754704 LacCer(d18:1/18:1) 0.073331926 0.053298592 0 LacCer(d18:1/18:0) 0.097210509 0 0.09068017 LacCer(d18:1/22:0) 0 0 0.338500303 LacCer(d18:1/24:1) 0 0.092433279 0 LacCer(d18:1/24:0) 0 0 0.034537728 LacCer(d18:1/26:1) 0 0 0 LacCer(d18:1/26:0) 0.019520366 0 0.049075767 Cer(d18:0/16:0) 0.827192721 0.959490725 7.166436435 Cer(d18:0/18:1) 0 0 0.040171863 Cer(d18:0/18:0) 0 0 0.195856123 Cer(d18:0/20:0) 0 0 0 Cer(d18:0/22:0) 0 0 0.416537403 Cer(d18:0/24:1) 0 0 1.087529251 Cer(d18:0/24:0) 0 0 0.114948774 MS_METABOLITE_DATA_END #METABOLITES METABOLITES_START metabolite_name Formula Mass MW structure Mass Info (precursor ion, product ion) Retention Times Human Metabolome Database InChIKey LipidMAPS Sphinganine C18H39NO2 301.2981 30476 1.8 HMDB0000269 OTKJDMGTUTTYMP-ZWKOTPCHSA-N LMSP01020001 Sphingosine C18H37NO2 299.2824 30474 1.52 WWUZIQQURGPMPG-KRWOKUGFSA-N LMSP01010001 Cer(d16:1/16:0) C32H63NO3 509.4808 3.97 Cer(d16:1/18:0) C34H67NO3 537.5121 30603 4.16 Cer(d18:1/14:0) C32H63NO3 509.4808 30562 3.96 Cer(d18:2/16:0) C34H65NO3 535.4964 30582 4 Cer(d18:1/16:1) C34H65NO3 535.4964 4.09 Cer(d18:1/16:0) C34H67NO3 537.5121 30565 4.16 Cer(d18:1/16:0(OH)) C34H67NO4 553.507 4.09 Cer(d18:2/18:1) C36H67NO3 561.5121 30583 4.07 Cer(d18:1/18:1) C36H69NO3 563.5277 30564 4.19 Cer(d18:1/18:0) C36H71NO3 565.5434 30566 4.33 Cer(d18:2/20:1) C38H71NO3 589.5434 30585 3.86 Cer(d18:2/20:0) C38H73NO3 591.559 30584 4.36 Cer(d18:1/20:0) C38H75NO3 593.5747 30567 4.48 Cer(d18:2/22:1) C40H75NO3 617.5747 4.39 Cer(d18:1/24:1) C42H81NO3 647.6216 30569 4.62 Cer(d18:1/24:0) C42H83NO3 649.6373 30572 4.75 Cer(d18:1/25:0) C43H85NO3 663.6529 30573 4.84 GlcCer(d18:1/14:0) 3.86 Cer(d18:1/26:1) C44H85NO3 675.6529 30570 4.78 Cer(d18:1/26:0) C44H87NO3 677.6686 30571 4.92 GlcCer(d18:1/16:1) C40H75NO8 697.5493 3.76 GlcCer(d18:1/16:0) C40H77NO8 699.5649 31063 4.06 GlcCer(d18:1/18:1) C42H79NO8 725.5806 31080 4.1 GlcCer(d18:1/18:0) C42H81NO8 727.5962 31065 4.23 GlcCer(d18:1/20:1) C44H83NO8 753.6119 4.26 GlcCer(d18:1/20:0) C44H85NO8 755.6275 31066 4.39 GlcCer(d18:1/22:0) C46H89NO8 783.6588 31067 4.52 GlcCer(d18:1/24:1) C48H91NO8 809.6745 31068 4.52 GlcCer(d18:1/24:0) C48H93NO8 811.6901 31069 4.65 GlcCer(d18:1/26:1) C50H95NO8 837.7058 31070 4.66 GlcCer(d18:1/26:0) C50H97NO8 839.7214 31071 4.8 LacCer(d18:1/16:0) C46H87NO13 861.6177 31136 4 LacCer(d18:1/18:1) C48H89NO13 887.6334 31144 4.06 LacCer(d18:1/18:0) C48H91NO13 889.649 31137 4.19 LacCer(d18:1/22:0) C52H99NO13 945.7116 31139 4.49 LacCer(d18:1/24:1) C54H101NO13 971.7273 31142 4.49 LacCer(d18:1/24:0) C54H103NO13 973.7429 31140 4.59 LacCer(d18:1/26:1) C56H105NO13 999.7586 31143 4.63 LacCer(d18:1/26:0) C56H107NO13 1001.7742 31141 4.76 Cer(d18:0/16:0) C34H69NO3 539.5277 30653 4.21 Cer(d18:0/18:1) C36H71NO3 565.5434 30661 4.26 Cer(d18:0/18:0) C36H73NO3 567.559 30654 4.37 Cer(d18:0/20:0) C38H77NO3 595.5903 30655 4.46 Cer(d18:0/22:0) C40H81NO3 623.6216 30656 4.59 Cer(d18:0/24:1) C42H83NO3 649.6373 30657 4.65 Cer(d18:0/24:0) C42H85NO3 651.6529 30658 4.78 METABOLITES_END #END