#METABOLOMICS WORKBENCH zhaom_20220406_224236 DATATRACK_ID:3181 STUDY_ID:ST002127 ANALYSIS_ID:AN003480
VERSION                          	1
CREATED_ON                       	05-31-2022
#PROJECT
PR:PROJECT_TITLE                 	Amino acid catabolism in hematopoietic cells
PR:PROJECT_SUMMARY               	Hematopoietic stem cells (HSCs) adapt their metabolism to maintenance and
PR:PROJECT_SUMMARY               	proliferation, but the mechanism remains incompletely understood. Here, we have
PR:PROJECT_SUMMARY               	investigated the total levels, uptake and catabolism of amino acid in
PR:PROJECT_SUMMARY               	hematopoietic stem cells, hemopoietic progenitors, and differentiated
PR:PROJECT_SUMMARY               	hematopoietic cells. We have also studied the catabolism of amino acid in
PR:PROJECT_SUMMARY               	hematopoietic stem cells under different conditions, such as homeostasis and
PR:PROJECT_SUMMARY               	proliferation and with drug treatment. Moreover, glycolytic metabolite, NAD+
PR:PROJECT_SUMMARY               	precursor nicotinamide riboside (NR), accelerated AA catabolism to activate GCN2
PR:PROJECT_SUMMARY               	and sustain long-term function of HSCs. Overall, our study uncovers the direct
PR:PROJECT_SUMMARY               	links between metabolic alterations and translation control in HSCs during
PR:PROJECT_SUMMARY               	homeostasis and proliferation.
PR:INSTITUTE                     	Sun Yat-sen University
PR:LAST_NAME                     	Zhao
PR:FIRST_NAME                    	Meng
PR:ADDRESS                       	Zhongshan 2nd Road
PR:EMAIL                         	zhaom38@mail.sysu.edu.cn
PR:PHONE                         	18138799889
PR:DOI                           	http://dx.doi.org/10.21228/M8GD8D
#STUDY
ST:STUDY_TITLE                   	Amino acids and TCA substrates in hematopoietic cells (Part4)
ST:STUDY_SUMMARY                 	This study uses [13C,15N] labeled amino acids to study the amino acid
ST:STUDY_SUMMARY                 	consumption and their catabolism into tricarboxylic acid cycle substrates in
ST:STUDY_SUMMARY                 	hematopoietic stem cells, hemopoietic progenitors, and differentiated
ST:STUDY_SUMMARY                 	hematopoietic cells under different conditions, such as homeostasis and
ST:STUDY_SUMMARY                 	proliferation and with drug treatment.
ST:INSTITUTE                     	Sun Yat-sen University
ST:LAST_NAME                     	Zhao
ST:FIRST_NAME                    	Meng
ST:ADDRESS                       	Zhongshan 2nd Road
ST:EMAIL                         	zhaom38@mail.sysu.edu.cn
ST:PHONE                         	18138799889
ST:SUBMIT_DATE                   	2022-04-06
#SUBJECT
SU:SUBJECT_TYPE                  	Mammal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nd-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nd-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nd-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_0h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-0h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_0h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-0h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_0h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-0h-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_12h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-12h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_12h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-12h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_12h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-12h-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_6h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-6h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_6h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-6h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_ND_6h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nd-6h-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nr-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nr-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	RAW_FILE_NAME=hsc-sot-nr-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_0h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-0h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_0h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-0h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_0h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-0h-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_12h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-12h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_12h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-12h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_12h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-12h-3.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_6h_1	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-6h-1.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_6h_2	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-6h-2.cdf
SUBJECT_SAMPLE_FACTORS           	-	HSC_sot_NR_6h_3	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	RAW_FILE_NAME=hsc-sot-nr-6h-3.cdf
#COLLECTION
CO:COLLECTION_SUMMARY            	5×10^5 indicated cells were incubated with 100 µM stable [13C,15N] amino acids
CO:COLLECTION_SUMMARY            	(MSK-A2-US-1.2, Cambridge Isotope Laboratories) for indicated time and
CO:COLLECTION_SUMMARY            	centrifuged at 500 g for 5 min at 4 °C. The pelleted cells were extracted in
CO:COLLECTION_SUMMARY            	500 µl ice-cold Acetonitrile: Isopropyl Alcohol: water (3:3:2 v/v/v) and
CO:COLLECTION_SUMMARY            	aliquoted as three technical replicates. The extracts were vortexed for 5 min at
CO:COLLECTION_SUMMARY            	4 °C and centrifuged at 14,000 g for 2 min at 4 °C. The supernatants were
CO:COLLECTION_SUMMARY            	dried by vacuum spin for subsequent derivatization and stored at -20 ℃.
CO:SAMPLE_TYPE                   	Bone marrow
#TREATMENT
TR:TREATMENT_SUMMARY             	Germ-free C57BL/6J mice were intraperitoneally injected with 10 mg/kg 5FU
TR:TREATMENT_SUMMARY             	(F6627-5G, Sigma-Aldrich) for 14 days, or fed with vehicle or NR (400 mg/kg per
TR:TREATMENT_SUMMARY             	day) (1341-23-7, ziyi-reagent) for consecutive 8 weeks (long-term) or 1 week
TR:TREATMENT_SUMMARY             	(short-term). Hematopoietic cells were stained and sorted from treated mice.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	To get the corresponding derivatives, the dried aliquots were incubated with 20
SP:SAMPLEPREP_SUMMARY            	µL 2% (w/v) methoxyamine hydrochloride (226904, Sigma-Aldrich) in pyridine for
SP:SAMPLEPREP_SUMMARY            	60 min at 37 °C, and silylated by 30 µL of
SP:SAMPLEPREP_SUMMARY            	N-Methyl-N-(tert-butyldimethylsilyl) trifluoroacetamide with 1%
SP:SAMPLEPREP_SUMMARY            	tert-Butyldimethylchlorosilane (TBDMS, 18162-48-6, Regis Technologies) for 30
SP:SAMPLEPREP_SUMMARY            	min at 45 °C. The corresponding derivatives were analyzed by GC-MS using the
SP:SAMPLEPREP_SUMMARY            	Trace 1310 gas chromatograph (Thermo Fisher) with the DB-35ms column (Agilent
SP:SAMPLEPREP_SUMMARY            	Technologies) connected to the Q ExactiveTM GC OrbitrapTM GC-MS/MS system
SP:SAMPLEPREP_SUMMARY            	(Thermo Fisher).
#CHROMATOGRAPHY
CH:INSTRUMENT_NAME               	TRACE 1310
CH:COLUMN_NAME                   	DB-35ms
CH:CHROMATOGRAPHY_TYPE           	GC
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Thermo Q Exactive Orbitrap
MS:INSTRUMENT_TYPE               	Orbitrap
MS:MS_TYPE                       	EI
MS:MS_COMMENTS                   	GC-MS data was acquired on Q-Exactive Orbitrap mass spectrometer (Thermo Fisher)
MS:MS_COMMENTS                   	coupled with Gas Chromatograph system TRACE 1310 (Thermo Fisher).
MS:MS_COMMENTS                   	Chromatographic separation was performed on a DB-35ms column module (30 m length
MS:MS_COMMENTS                   	x 0.25 mm internal diameter, Agilent Technologies). The column temperature was
MS:MS_COMMENTS                   	programmed with an initial temperature of 50 °C for 2 min, then ramped at
MS:MS_COMMENTS                   	10°C/min to 325 °C, and maintained for 5 min. The mass range was set as 50-600
MS:MS_COMMENTS                   	m/z, and the resolution was 60,000. The ion source temperature was 300°C with
MS:MS_COMMENTS                   	the transfer line temperature of 250°C, and the electron energy was 70 eV with
MS:MS_COMMENTS                   	EI source.
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	Peak Area
MS_METABOLITE_DATA_START
Samples	HSC_sot_ND_1	HSC_sot_ND_2	HSC_sot_ND_3	HSC_sot_ND_0h_1	HSC_sot_ND_0h_2	HSC_sot_ND_0h_3	HSC_sot_ND_12h_1	HSC_sot_ND_12h_2	HSC_sot_ND_12h_3	HSC_sot_ND_6h_1	HSC_sot_ND_6h_2	HSC_sot_ND_6h_3	HSC_sot_NR_1	HSC_sot_NR_2	HSC_sot_NR_3	HSC_sot_NR_0h_1	HSC_sot_NR_0h_2	HSC_sot_NR_0h_3	HSC_sot_NR_12h_1	HSC_sot_NR_12h_2	HSC_sot_NR_12h_3	HSC_sot_NR_6h_1	HSC_sot_NR_6h_2	HSC_sot_NR_6h_3
Factors	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ctrl, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 1 h | Batch:1e | Note:[13C, 15N]AAs were used for AA uptake (FigS6.J)	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:NR 1 week, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1e | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig5.L).	
[13C_ 15N]Alanine_ 2TBDMS	331000.0000	317000.0000	310000.0000	3310000.0000	3170000.0000	3100000.0000	875000.0000	921000.0000	830000.0000	1600000.0000	1410000.0000	1360000.0000	332000.0000	299000.0000	312000.0000	3320000.0000	2990000.0000	3120000.0000	753000.0000	727000.0000	691000.0000	1330000.0000	1240000.0000	1290000.0000
[13C_ 15N]Aspartic acid_ 3TBDMS	82500.0000	83500.0000	74300.0000	825000.0000	835000.0000	743000.0000	365000.0000	321000.0000	333000.0000	599000.0000	435000.0000	509000.0000	84000.0000	76900.0000	79700.0000	840000.0000	769000.0000	797000.0000	313000.0000	303000.0000	296000.0000	543000.0000	486000.0000	423000.0000
[13C_ 15N]Glutamic acid_ 3TBDMS	61300.0000	63800.0000	60700.0000	613000.0000	638000.0000	607000.0000	235000.0000	244000.0000	207000.0000	395000.0000	407000.0000	385000.0000	66700.0000	57100.0000	59100.0000	667000.0000	571000.0000	591000.0000	184000.0000	182000.0000	154000.0000	310000.0000	279000.0000	288000.0000
[13C_ 15N]Glycine_ 2TBDMS	51100.0000	63400.0000	50800.0000	6350000.0000	5500000.0000	5380000.0000	3040000.0000	3010000.0000	2070000.0000	3840000.0000	4870000.0000	4100000.0000	58700.0000	59500.0000	57400.0000	6710000.0000	5780000.0000	5350000.0000	3130000.0000	2930000.0000	3380000.0000	3880000.0000	4920000.0000	4900000.0000
[13C_ 15N]Histidine_ 3TBDMS	64800.0000	56500.0000	57700.0000	648000.0000	565000.0000	577000.0000	173000.0000	127000.0000	208000.0000	314000.0000	313000.0000	354000.0000	54600.0000	54400.0000	49500.0000	546000.0000	544000.0000	495000.0000	102000.0000	136000.0000	138000.0000	221000.0000	314000.0000	242000.0000
[13C_ 15N]Isoleucine_ 2TBDMS	328000.0000	306000.0000	281000.0000	3280000.0000	3060000.0000	2810000.0000	1400000.0000	1430000.0000	1100000.0000	2150000.0000	2250000.0000	2140000.0000	296000.0000	384000.0000	357000.0000	2960000.0000	3840000.0000	3570000.0000	1370000.0000	1040000.0000	995000.0000	2270000.0000	2300000.0000	2130000.0000
[13C_ 15N]Leucine_ 2TBDMS	369000.0000	353000.0000	318000.0000	3690000.0000	3530000.0000	3180000.0000	1040000.0000	984000.0000	1080000.0000	2120000.0000	2240000.0000	2140000.0000	302000.0000	353000.0000	321000.0000	3020000.0000	3530000.0000	3210000.0000	782000.0000	810000.0000	741000.0000	1460000.0000	1580000.0000	1900000.0000
[13C_ 15N]Lysine_ 3TBDMS	148000.0000	139000.0000	133000.0000	1480000.0000	1390000.0000	1330000.0000	594000.0000	551000.0000	585000.0000	813000.0000	786000.0000	796000.0000	134000.0000	142000.0000	166000.0000	1340000.0000	1420000.0000	1660000.0000	466000.0000	441000.0000	464000.0000	766000.0000	780000.0000	837000.0000
[13C_ 15N]Methionine_ 2TBDMS	197000.0000	206000.0000	182000.0000	1970000.0000	2060000.0000	1820000.0000	740000.0000	680000.0000	544000.0000	1200000.0000	1180000.0000	927000.0000	200000.0000	220000.0000	173000.0000	2000000.0000	2200000.0000	1730000.0000	501000.0000	575000.0000	607000.0000	1010000.0000	1270000.0000	1040000.0000
[13C_ 15N]Phenylalanine_ 2TBDMS	289000.0000	297000.0000	243000.0000	2890000.0000	2970000.0000	2430000.0000	1240000.0000	1380000.0000	1130000.0000	1410000.0000	1520000.0000	1440000.0000	246000.0000	276000.0000	222000.0000	2460000.0000	2760000.0000	2220000.0000	1000000.0000	929000.0000	926000.0000	1360000.0000	1240000.0000	1360000.0000
[13C_ 15N]Proline_ 2TBDMS	184000.0000	168000.0000	174000.0000	1840000.0000	1680000.0000	1740000.0000	450000.0000	528000.0000	423000.0000	866000.0000	829000.0000	857000.0000	176000.0000	161000.0000	160000.0000	1760000.0000	1610000.0000	1600000.0000	319000.0000	275000.0000	325000.0000	750000.0000	701000.0000	731000.0000
[13C_ 15N]Serine_ 3TBDMS	321000.0000	324000.0000	282000.0000	3210000.0000	3240000.0000	2820000.0000	964000.0000	851000.0000	886000.0000	2120000.0000	2190000.0000	1860000.0000	347000.0000	311000.0000	356000.0000	3470000.0000	3110000.0000	3560000.0000	712000.0000	793000.0000	822000.0000	1940000.0000	1880000.0000	1650000.0000
[13C_ 15N]Threonine_ 3TBDMS	86000.0000	79700.0000	77200.0000	860000.0000	797000.0000	772000.0000	342000.0000	313000.0000	322000.0000	510000.0000	508000.0000	413000.0000	61200.0000	67200.0000	85200.0000	612000.0000	672000.0000	852000.0000	286000.0000	244000.0000	232000.0000	362000.0000	350000.0000	368000.0000
[13C_ 15N]Tyrosine_ 3TBDMS	798000.0000	774000.0000	724000.0000	7980000.0000	7740000.0000	7240000.0000	2250000.0000	2370000.0000	2940000.0000	4140000.0000	4380000.0000	3180000.0000	730000.0000	698000.0000	740000.0000	7300000.0000	6980000.0000	7400000.0000	2210000.0000	1830000.0000	1850000.0000	3120000.0000	3970000.0000	3320000.0000
[13C_ 15N]Valine_ 2TBDMS	805000.0000	762000.0000	793000.0000	8050000.0000	7620000.0000	7930000.0000	3210000.0000	2980000.0000	2570000.0000	5270000.0000	4440000.0000	4280000.0000	822000.0000	769000.0000	787000.0000	8220000.0000	7690000.0000	7870000.0000	1790000.0000	2280000.0000	2610000.0000	4020000.0000	4230000.0000	4080000.0000
[13C]Alpha_Ketoglutarate				2160000.0000	1880000.0000	2000000.0000	34000.0000	37400.0000	41200.0000	26100.0000	28500.0000	30100.0000				23500.0000	20500.0000	21700.0000	50900.0000	51500.0000	50900.0000	33400.0000	32100.0000	35000.0000
[13C]Citrate				45400.0000	42100.0000	39700.0000	81800.0000	80700.0000	86800.0000	70200.0000	69300.0000	69800.0000				48900.0000	55500.0000	46700.0000	107000.0000	90600.0000	95600.0000	82200.0000	84200.0000	82400.0000
[13C]Fumatate				173000.0000	176000.0000	142000.0000	343000.0000	315000.0000	342000.0000	244000.0000	249000.0000	275000.0000				159000.0000	138000.0000	138000.0000	364000.0000	354000.0000	367000.0000	293000.0000	276000.0000	285000.0000
[13C]Malate				84900.0000	90700.0000	104000.0000	142000.0000	162000.0000	145000.0000	116000.0000	136000.0000	133000.0000				108000.0000	137000.0000	119000.0000	164000.0000	178000.0000	184000.0000	141000.0000	150000.0000	156000.0000
[13C]Succinate				128000.0000	135000.0000	113000.0000	213000.0000	235000.0000	231000.0000	192000.0000	160000.0000	185000.0000				108000.0000	111000.0000	123000.0000	247000.0000	246000.0000	267000.0000	209000.0000	192000.0000	206000.0000
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	pubchem_id	inchi_key	kegg_id	other_id	other_id_type	ri	ri_type	moverz_quant	
[13C, 15N]Alanine, 2TBDMS						15.06			
[13C, 15N]Aspartic acid, 3TBDMS						21.49			
[13C, 15N]Glutamic acid, 3TBDMS						22.54			
[13C, 15N]Glycine, 2TBDMS						15.39			
[13C, 15N]Histidine, 3TBDMS						25.11			
[13C, 15N]Isoleucine, 2TBDMS						17.26			
[13C, 15N]Leucine, 2TBDMS						16.91			
[13C, 15N]Lysine, 3TBDMS						23.48			
[13C, 15N]Methionine, 2TBDMS						19.74			
[13C, 15N]Phenylalanine, 2TBDMS						20.92			
[13C, 15N]Proline, 2TBDMS						20.49			
[13C, 15N]Serine, 3TBDMS						19.94			
[13C, 15N]Threonine, 3TBDMS						20.22			
[13C, 15N]Tyrosine, 3TBDMS						25.51			
[13C, 15N]Valine, 2TBDMS						16.46			
[13C]Alpha_Ketoglutarate						21.03			
[13C]Citrate						26.51			
[13C]Fumatate						18.77			
[13C]Malate						22.05			
[13C]Succinate						18.37			
METABOLITES_END
#END