#METABOLOMICS WORKBENCH lvhuizhen_20240225_234135 DATATRACK_ID:4674 STUDY_ID:ST003244 ANALYSIS_ID:AN005314 PROJECT_ID:PR002014
VERSION             	1
CREATED_ON             	June 7, 2024, 11:12 am
#PROJECT
PR:PROJECT_TITLE                 	Suppression of prostaglandin I2–type I interferon axis induces extramedullary
PR:PROJECT_TITLE                 	hematopoiesis to promote cardiac repair after myocardial infarction
PR:PROJECT_SUMMARY               	Background: Immune cells are closely associated with all processes of cardiac
PR:PROJECT_SUMMARY               	repair following myocardial infarction (MI), including the initiation,
PR:PROJECT_SUMMARY               	development, and resolution of inflammation. Spleen extramedullary hematopoiesis
PR:PROJECT_SUMMARY               	(EMH) serves as a critical source of emergency mature blood cells that are
PR:PROJECT_SUMMARY               	generated through the self-renewal and differentiation of hematopoietic
PR:PROJECT_SUMMARY               	stem/progenitor cells (HSPCs). However, how EMH responds to MI and the role of
PR:PROJECT_SUMMARY               	EMH in cardiac repair post-MI remains unclear. Methods: To assess the role of
PR:PROJECT_SUMMARY               	spleen EMH in MI, a Tcf21CreERScfflox/flox MI mouse model with inhibited EMH was
PR:PROJECT_SUMMARY               	constructed. GFP+ HSCs sorted from eGFP mouse spleen by flow cytometry and
PR:PROJECT_SUMMARY               	injected into Tcf21CreERScfflox/flox mice to test the sources of local
PR:PROJECT_SUMMARY               	inflammatory cells during MI. Using highly specific liquid chromatography-tandem
PR:PROJECT_SUMMARY               	mass spectrometry and single-cell RNA sequencing, we analyzed the lipidomic
PR:PROJECT_SUMMARY               	profile of arachidonic acid metabolites and the transcriptomes of HSPCs in the
PR:PROJECT_SUMMARY               	spleen after MI. Results: We found that MI enhanced EMH, as reflected by the
PR:PROJECT_SUMMARY               	increase in spleen weight and volume and the number of HSPCs in the spleen. The
PR:PROJECT_SUMMARY               	lack of EMH in Scf-deficient mice exacerbated tissue injury post-MI. Analyzing
PR:PROJECT_SUMMARY               	the transcriptome of spleen HSPCs post-MI, we found the type I interferon (IFN)
PR:PROJECT_SUMMARY               	pathway significantly inhibited in HSC/multipotent progenitor subclusters and
PR:PROJECT_SUMMARY               	the absence of type I IFN signaling enhanced the MI-induced spleen EMH.
PR:PROJECT_SUMMARY               	Lipidomics analysis revealed that prostaglandin I2 (PGI2) was markedly reduced
PR:PROJECT_SUMMARY               	in the spleen. Mechanistically, PGI2 suppressed MI-induced EMH through a PGI2
PR:PROJECT_SUMMARY               	receptor (IP)-cAMP-453p-SP1 cascade in spleen HSPCs. Finally, hematopoietic
PR:PROJECT_SUMMARY               	cell-specific IP-deficient mice exhibited enhanced EMH and improved cardiac
PR:PROJECT_SUMMARY               	recovery post-MI, which mitigated the adverse secondary outcomes of treatment
PR:PROJECT_SUMMARY               	with cicaprost, a PGI2 analog and anti-inflammatory agent. Conclusions:
PR:PROJECT_SUMMARY               	Together, our findings revealed that a PGI2–IFN axis was involved in spleen
PR:PROJECT_SUMMARY               	EMH after MI, providing new mechanistic insights into spleen EMH post-MI and
PR:PROJECT_SUMMARY               	offering a new therapeutic target for treating ischemic cardiac injury.
PR:INSTITUTE                     	Tianjin Medical University
PR:LABORATORY                    	Metabolic cardiovascular disease lab
PR:LAST_NAME                     	Lv
PR:FIRST_NAME                    	Huizhen
PR:ADDRESS                       	Qixiangtai Road 22th, Tianjin, Tianjin, 300070, China
PR:EMAIL                         	lvhuizhen@tmu.edu.cn
PR:PHONE                         	83336591
#STUDY
ST:STUDY_TITLE                   	Suppression of prostaglandin I2–type I interferon axis induces extramedullary
ST:STUDY_TITLE                   	hematopoiesis to promote cardiac repair after myocardial infarction
ST:STUDY_SUMMARY                 	Background: Immune cells are closely associated with all processes of cardiac
ST:STUDY_SUMMARY                 	repair following myocardial infarction (MI), including the initiation,
ST:STUDY_SUMMARY                 	development, and resolution of inflammation. Spleen extramedullary hematopoiesis
ST:STUDY_SUMMARY                 	(EMH) serves as a critical source of emergency mature blood cells that are
ST:STUDY_SUMMARY                 	generated through the self-renewal and differentiation of hematopoietic
ST:STUDY_SUMMARY                 	stem/progenitor cells (HSPCs). However, how EMH responds to MI and the role of
ST:STUDY_SUMMARY                 	EMH in cardiac repair post-MI remains unclear. Methods: To assess the role of
ST:STUDY_SUMMARY                 	spleen EMH in MI, a Tcf21CreERScfflox/flox MI mouse model with inhibited EMH was
ST:STUDY_SUMMARY                 	constructed. GFP+ HSCs sorted from eGFP mouse spleen by flow cytometry and
ST:STUDY_SUMMARY                 	injected into Tcf21CreERScfflox/flox mice to test the sources of local
ST:STUDY_SUMMARY                 	inflammatory cells during MI. Using highly specific liquid chromatography-tandem
ST:STUDY_SUMMARY                 	mass spectrometry and single-cell RNA sequencing, we analyzed the lipidomic
ST:STUDY_SUMMARY                 	profile of arachidonic acid metabolites and the transcriptomes of HSPCs in the
ST:STUDY_SUMMARY                 	spleen after MI. Results: We found that MI enhanced EMH, as reflected by the
ST:STUDY_SUMMARY                 	increase in spleen weight and volume and the number of HSPCs in the spleen. The
ST:STUDY_SUMMARY                 	lack of EMH in Scf-deficient mice exacerbated tissue injury post-MI. Analyzing
ST:STUDY_SUMMARY                 	the transcriptome of spleen HSPCs post-MI, we found the type I interferon (IFN)
ST:STUDY_SUMMARY                 	pathway significantly inhibited in HSC/multipotent progenitor subclusters and
ST:STUDY_SUMMARY                 	the absence of type I IFN signaling enhanced the MI-induced spleen EMH.
ST:STUDY_SUMMARY                 	Lipidomics analysis revealed that prostaglandin I2 (PGI2) was markedly reduced
ST:STUDY_SUMMARY                 	in the spleen. Mechanistically, PGI2 suppressed MI-induced EMH through a PGI2
ST:STUDY_SUMMARY                 	receptor (IP)-cAMP-453p-SP1 cascade in spleen HSPCs. Finally, hematopoietic
ST:STUDY_SUMMARY                 	cell-specific IP-deficient mice exhibited enhanced EMH and improved cardiac
ST:STUDY_SUMMARY                 	recovery post-MI, which mitigated the adverse secondary outcomes of treatment
ST:STUDY_SUMMARY                 	with cicaprost, a PGI2 analog and anti-inflammatory agent. Conclusions:
ST:STUDY_SUMMARY                 	Together, our findings revealed that a PGI2–IFN axis was involved in spleen
ST:STUDY_SUMMARY                 	EMH after MI, providing new mechanistic insights into spleen EMH post-MI and
ST:STUDY_SUMMARY                 	offering a new therapeutic target for treating ischemic cardiac injury.
ST:INSTITUTE                     	Tianjin Medical University
ST:LAST_NAME                     	Lv
ST:FIRST_NAME                    	Huizhen
ST:ADDRESS                       	Qixiangtai Road 22th, Tianjin, Tianjin, 300070, China
ST:EMAIL                         	lvhuizhen@tmu.edu.cn
ST:PHONE                         	13212161520
#SUBJECT
SU:SUBJECT_TYPE                  	Mammal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
#FACTORS
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Sham-1	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-1
SUBJECT_SAMPLE_FACTORS           	-	Sham-2	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-2
SUBJECT_SAMPLE_FACTORS           	-	Sham-3	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-3
SUBJECT_SAMPLE_FACTORS           	-	Sham-4	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-4
SUBJECT_SAMPLE_FACTORS           	-	Sham-5	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-5
SUBJECT_SAMPLE_FACTORS           	-	Sham-6	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-6
SUBJECT_SAMPLE_FACTORS           	-	Sham-7	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-7
SUBJECT_SAMPLE_FACTORS           	-	Sham-8	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-8
SUBJECT_SAMPLE_FACTORS           	-	Sham-9	Sample source:Spleen | treatment:Sham	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-9
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-1	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-10
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-2	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-11
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-3	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-12
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-4	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-13
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-5	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-14
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-6	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-15
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-7	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-16
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-8	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-17
SUBJECT_SAMPLE_FACTORS           	-	MI 1d-9	Sample source:Spleen | treatment:MI1d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-18
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-1	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-19
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-2	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-20
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-3	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-21
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-4	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-22
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-5	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-23
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-6	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-24
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-7	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-25
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-8	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-26
SUBJECT_SAMPLE_FACTORS           	-	MI 3d-9	Sample source:Spleen | treatment:MI 3d	RAW_FILE_NAME( raw data file names)=Data_2_eico_lvhuizhen_48-27
#COLLECTION
CO:COLLECTION_SUMMARY            	Spleen samples from mice subjected to myocardial infarction (MI) surgery were
CO:COLLECTION_SUMMARY            	extracted with liquid–liquid extraction.
CO:SAMPLE_TYPE                   	Spleen
CO:STORAGE_CONDITIONS            	-80℃
#TREATMENT
TR:TREATMENT_SUMMARY             	No treatment
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	50 mg of spleen tissues was homogenized with methanol (2% formic acid and 0.01
SP:SAMPLEPREP_SUMMARY            	mol/L BHT) spiked with internal standard mixture. After centrifugation, the
SP:SAMPLEPREP_SUMMARY            	supernatant was added to water and ethylacetate, and the sample was mixed and
SP:SAMPLEPREP_SUMMARY            	centrifuged at 12,000 × g. The upper organic phase was transferred to a new
SP:SAMPLEPREP_SUMMARY            	tube, and the water phase was extracted again. The organic phase was combined
SP:SAMPLEPREP_SUMMARY            	and then evaporated to dryness and further dissolved in 100 μL of 30%
SP:SAMPLEPREP_SUMMARY            	acetonitrile. After vigorous mixing, samples were filtered by use of centrifuge
SP:SAMPLEPREP_SUMMARY            	tube filters (nylon membrane, 0.22 μm).
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	Reversed phase
CH:INSTRUMENT_NAME               	Waters Acquity
CH:COLUMN_NAME                   	Waters ACQUITY UPLC BEH C18 (50 x 2.1mm,1.7um)
CH:SOLVENT_A                     	100% water; 0.3% ethanoic acid
CH:SOLVENT_B                     	100% acetonitrile
CH:FLOW_GRADIENT                 	0-3min:70%A:30%B,3-20min:40%A:60%B,
CH:FLOW_GRADIENT                 	20-27min:20%A:80%B,27-30min:70%A;30%B
CH:FLOW_RATE                     	0.25mL/min
CH:COLUMN_TEMPERATURE            	25
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	ABI Sciex 5500 QTrap
MS:INSTRUMENT_TYPE               	QTRAP
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:MS_COMMENTS                   	Arachidonic acid metabolites were quantified by use of a 5500 QTRAP hybrid
MS:MS_COMMENTS                   	triple quadrupole linear ion trap mass spectrometer (AB Sciex, Foster City, CA,
MS:MS_COMMENTS                   	USA) equipped with a Turbo Ion Spray electrospray ionization source. The mass
MS:MS_COMMENTS                   	spectrometer was operated using the software Analyst 1.5.1. Analytes were
MS:MS_COMMENTS                   	detected using multiple reaction monitoring (MRM) scans in negative mode. The
MS:MS_COMMENTS                   	dwell time used for all MRM experiments was 25 ms. The ion source parameters
MS:MS_COMMENTS                   	were set as follows: CUR  =  40 psi, GS1  =  30 psi, GS2  =  30 psi,
MS:MS_COMMENTS                   	IS  =  −4500 V, CAD  =  medium, and temp  =  500°C. Metaboanalyst
MS:MS_COMMENTS                   	3.0 (http://www.metaboanalyst.ca) was used for metabolomic data analysis.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	ng/mg of tissue
MS_METABOLITE_DATA_START
Samples	Sham-1	Sham-2	Sham-3	Sham-4	Sham-5	Sham-6	Sham-7	Sham-8	Sham-9	MI 1d-1	MI 1d-2	MI 1d-3	MI 1d-4	MI 1d-5	MI 1d-6	MI 1d-7	MI 1d-8	MI 1d-9	MI 3d-1	MI 3d-2	MI 3d-3	MI 3d-4	MI 3d-5	MI 3d-6	MI 3d-7	MI 3d-8	MI 3d-9
Factors	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:Sham	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI1d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d	Sample source:Spleen | treatment:MI 3d
AA_COX_6k-PGF1a	1.05	1.14	1.16	1.20	1.25	1.42	1.52	1.57	1.97	0.25	1.16	1.24	0.25	1.25	1.26	1.28	1.43	0.16	0.08	0.66	0.78	0.07	0.06	0.92	0.94	0.94	1.01
AA_COX_PGD2	2.67	2.02	2.65	2.01	2.69	2.66	2.35	3.20	2.43	0.86	2.60	2.63	0.71	2.78	2.49	2.91	2.55	0.43	0.12	1.55	1.55	0.22	0.14	2.06	2.31	1.99	2.62
AA_COX_15d-PGJ2	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00
AA_COX_PGB2	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00	0.00
AA_COX_PGE2	0.51	0.54	0.62	0.49	0.68	0.39	0.58	0.80	0.71	0.12	0.64	0.63	0.10	0.62	0.62	0.68	0.65	0.06	0.02	0.24	0.30	0.03	0.02	0.44	0.40	0.34	0.55
AA_COX_PGF2a	0.06	0.06	0.08	0.05	0.08	0.06	0.06	0.10	0.06	0.01	0.09	0.07	0.02	0.08	0.08	0.07	0.07	0.01	0.00	0.05	0.04	0.00	0.00	0.09	0.05	0.04	0.06
AA_COX_PGJ2	0.03	0.03	0.02	0.02	0.04	0.02	0.02	0.06	0.02	0.00	0.04	0.04	0.00	0.03	0.02	0.04	0.02	0.00	0.00	0.01	0.01	0.00	0.00	0.02	0.02	0.01	0.04
AA_COX_TXB2	0.23	0.22	0.28	0.21	0.27	0.23	0.24	0.31	0.24	0.06	0.28	0.27	0.06	0.28	0.27	0.31	0.29	0.03	0.01	0.16	0.18	0.02	0.01	0.22	0.21	0.23	0.25
AA_LOX_11-HETE	1.04	0.92	0.82	0.83	1.13	0.96	1.11	1.21	1.27	0.15	1.11	1.18	0.17	1.29	1.52	1.36	1.14	0.10	0.03	0.46	0.43	0.04	0.04	0.86	0.85	0.59	1.15
AA_LOX_12-HETE	3.87	11.80	12.50	4.25	13.59	12.49	10.30	9.74	3.34	0.55	24.46	6.23	0.63	5.11	8.95	5.74	6.51	0.43	0.14	1.72	5.30	0.12	0.10	15.58	6.73	6.27	7.26
AA_LOX_15-HETE	0.98	0.72	0.63	0.77	0.84	0.60	0.94	1.00	0.82	0.15	0.84	0.95	0.25	1.01	1.09	0.95	0.71	0.12	0.05	0.40	0.27	0.05	0.03	0.65	0.63	0.45	0.97
AA_LOX_15-oxo-ETE	0.002409956	0.001532624	0.001613604	0.002338645	0.00170946	0.002797267	0.003836576	0.001952622	0.003850409	0.000357583	0.002055459	0.002515349	0.000738419	0.002101508	0.003487624	0.002644413	0.003946888	0.003213431	0.001946889	0.000626202	0.00096191	0.000162622	0.000971286	0.002619516	0.001551862	0.001223242	0.002172712
AA_LOX_5-HETE	0.027932526	0.037928319	0.202144734	0.043274949	0.06116742	0.041279395	0.063962025	0.060255403	0.026342497	0.023595074	0.069691661	0.052677639	0.055174281	0.034349704	0.039310253	0.046780287	0.060636874	0.065518715	0.046397559	0.037335355	0.042499965	0.038234793	0.03145908	0.061105901	0.039760849	0.062526751	0.055116653
AA_LOX_5-oxo-ETE	0.00101255	0.001971416	0.004525831	0.001034923	0.001269489	0.003380108	0.003643455	0.001513189	0.001319479	0.00086096	0.003422661	0.000767154	0.004564144	0.002150404	0.002049362	0.001288748	0.00489081	0.012040301	0.002800802	0.000901782	0.004436582	0.002752644	0.003162656	0.001579587	0.001343931	0.005464265	0.001900404
AA_LOX_6S-LXA4	0.000145033	0.0000679	0.000249423	0.000118506	0.000164676	0.000173091	0.000181115	0.000216246	0.000144219	0.0000523	0.000066	0.00013944	0.000126383	0.000124849	0.000227307	0.000140048	0.000161348	0.000138304	0.0000799	0.0000819	0.000121096	0.0000939	0.0000502	0.000098	0.00013712	0.000066	0.000151197
AA_LOX_8-HETE	0.023744583	0.054924533	0.049023844	0.023575332	0.058353912	0.079289283	0.037813593	0.038950032	0.020088235	0.004768437	0.100543132	0.029971608	0.008991937	0.023104165	0.047885652	0.027674879	0.047394221	0.004543164	0.005969483	0.010421346	0.036828913	0.005307692	0.00182904	0.059795743	0.037086925	0.047452268	0.030240401
AA_LOX_9-HETE	0.007295621	0.011002488	0.008192	0.006119154	0.014340378	0.009365577	0.008594754	0.011371206	0.00799454	0.00288256	0.017195192	0.008236151	0.001014529	0.007524789	0.010816241	0.006776366	0.01262844	0.00241221	0.002396591	0.004969957	0.006334453	0.003066016	0.00517978	0.00813996	0.008289194	0.015963906	0.00631243
AA_LOX_LTB4	0.002271877	0.006051621	0.009203877	0.00397283	0.0101093	0.005690528	0.003176524	0.007841132	0.001455883	0.000234541	0.010274134	0.003015295	0.000800788	0.003344209	0.002783428	0.003591388	0.002315991	0.00048532	0.000214958	0.000966328	0.003333185	0.00035384	0.000120266	0.009043062	0.003094596	0.004526602	0.002801694
AA_P450_11,12 DHET	0.00040079	0.000401592	0.000420748	0.000269552	0.000645826	0.001181929	0.000448872	0.000634598	0.000687993	0.000298442	0.000482548	0.000413823	0.000302653	0.000503133	0.000764535	0.000482428	0.000674604	0.000492168	0.000242351	0.000429024	0.000635374	0.000181805	0.000230282	0.00050755	0.000487258	0.000698179	0.000640395
AA_P450_11,12-EET	0.001683118	0.000609304	0.00056345	0.000093	0.000250702	0.0009142	0.002886204	0.000561975	0.000453411	0.000270243	0.002214996	0.000394409	0.000751391	0.000632992	0.000805489	0.00018057	0.002850797	0.006012438	0.000127464	0.000392109	0.001211135	0.0000523	0.000705238	0.002454158	0.000419311	0.001465909	0.000252531
AA_P450_14,15 DHET	0.000760168	0.001182643	0.000895647	0.001001846	0.001108592	0.001011573	0.001350773	0.001442812	0.001360733	0.000493765	0.001687366	0.00095773	0.000704474	0.001487014	0.00170882	0.001682204	0.001651927	0.000826726	0.000518124	0.000390575	0.001521254	0.000711281	0.000506318	0.001339538	0.000967465	0.001808827	0.001451008
AA_P450_18-HETE	0.001081858	0.000657614	0.000891901	0.001245989	0.000986232	0.001578849	0.000911818	0.00089479	0.001379011	0.000201357	0.001345789	0.001295374	0.000309537	0.001248734	0.002304486	0.000743183	0.002008279	0.000332721	0.000467921	0.000568623	0.001402724	0.00004	0.000332722	0.000963705	0.001740116	0.003126812	0.000571019
AA_P450_5,6 DHET	0.000311983	0.0006921	0.00073283	0.000343147	0.000821177	0.000168613	0.000612264	0.001331133	0.000189608	0.000332599	0.000731727	0.000520814	0.000916645	0.000433882	0.00040085	0.000737963	0.000369149	0.002398183	0.001174243	0.001041785	0.000626279	0.000822585	0.000957739	0.001396468	0.000253932	0.001362183	0.000798327
AA_P450_8,9 DHET	0.000140118	0.000418255	0.00021897	0.000256406	0.000295539	0.000546618	0.000157428	0.000865373	0.000257253	0.0000431	0.000318861	0.000181693	0.000193483	0.000351441	0.000244099	0.000336914	0.00069002	0.000311104	0.00021218	0.000337393	0.000157057	0.000178004	0.000136387	0.000299215	0.000315906	0.00064426	0.000468815
AA_P450_8,9-EET	0.001170465	0.002936516	0.008641766	0.001372076	0.004724973	0.009308307	0.003327657	0.003548665	0.002793081	0.00091554	0.001252152	0.000300729	0.001318327	0.000769279	0.00078899	0.000574555	0.004667413	0.002615436	0.000471854	0.000433034	0.003217061	0.002589999	0.001131542	0.005684427	0.000953105	0.004199676	0.002420551
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	Pubchem ID	Kegg ID
AA_COX_6k-PGF1a	5280888	C05961
AA_COX_PGD2	448457	C00696
AA_COX_15d-PGJ2	5311211	C14717
AA_COX_PGB2	5280881	C05954
AA_COX_PGE2	5280360	C00584
AA_COX_PGF2a	5280363	C00639
AA_COX_PGJ2	5280884	C05957
AA_COX_TXB2	5283137	C05963
AA_LOX_11-HETE	14123410
AA_LOX_12-HETE	13786989	C14777
AA_LOX_15-HETE	9966861	C21482
AA_LOX_15-oxo-ETE	5280701	C04577
AA_LOX_5-HETE	5280733	C04805
AA_LOX_5-oxo-ETE	5283159	C14732
AA_LOX_6S-LXA4	42607306
AA_LOX_8-HETE	11976122
AA_LOX_9-HETE	14123398
AA_LOX_LTB4	5280492	C02165
AA_P450_11,12 DHET	5283146	C14774
AA_P450_11,12-EET	5283204	C14770
AA_P450_14,15 DHET	5283147	C14775
AA_P450_18-HETE	6442778
AA_P450_5,6 DHET	5283142	C14772
AA_P450_8,9 DHET	5283144	C14773
AA_P450_8,9-EET	5283203	C14769
METABOLITES_END
#END