#METABOLOMICS WORKBENCH aferrarini_20200727_085446 DATATRACK_ID:2103 STUDY_ID:ST001434 ANALYSIS_ID:AN002397 PROJECT_ID:PR000985
VERSION             	1
CREATED_ON             	July 28, 2020, 11:10 am
#PROJECT
PR:PROJECT_TITLE                 	ALDH4A1 is a novel atherosclerosis auto-antigen and a target of protective 6
PR:PROJECT_TITLE                 	antibodies
PR:PROJECT_TYPE                  	LC-MS Untargeted Lipidomics
PR:PROJECT_SUMMARY               	Cardiovascular disease (CVD) is the leading cause of mortality in the world,
PR:PROJECT_SUMMARY               	with most CVD deaths resulting from myocardial infarction and stroke. The main
PR:PROJECT_SUMMARY               	cause underlying thrombosis and cardiovascular events is atherosclerosis, an
PR:PROJECT_SUMMARY               	inflammatory disease that can remain asymptomatic for long periods of time.
PR:PROJECT_SUMMARY               	There is an urgent need for new therapeutic and diagnostic options in this area.
PR:PROJECT_SUMMARY               	Atherosclerotic plaques have long been known to contain autoantibodies 1, 2, and
PR:PROJECT_SUMMARY               	there is a well-accepted connection between atherosclerosis and autoimmunity 3.
PR:PROJECT_SUMMARY               	However, the immunogenic trigger and the impact of the autoantibody response
PR:PROJECT_SUMMARY               	during atherosclerosis are not well understood 3, 4, 5. Here we performed a
PR:PROJECT_SUMMARY               	high-throughput single-cell analysis of the atherosclerosis-associated antibody
PR:PROJECT_SUMMARY               	repertoire. Antibody gene sequencing of more than 1700 B cells from atherogenic
PR:PROJECT_SUMMARY               	LDLR-/- mice and control animals identified 56 antibodies expressed by
PR:PROJECT_SUMMARY               	in-vivo-expanded clones of B lymphocytes in the context of atherosclerosis. A
PR:PROJECT_SUMMARY               	third of the expanded antibodies showed reactivity against the atherosclerotic
PR:PROJECT_SUMMARY               	plaque, indicating that various antigens in the lesion can trigger antibody
PR:PROJECT_SUMMARY               	responses. A deep proteomics analysis revealed aldehyde dehydrogenase 4 family
PR:PROJECT_SUMMARY               	member A1 (ALDH4A1), a mitochondrial dehydrogenase involved in proline
PR:PROJECT_SUMMARY               	metabolism, as target antigen of one of these autoantibodies, A12. We show that
PR:PROJECT_SUMMARY               	ALDH4A1 distribution is altered during atherosclerosis and circulating levels of
PR:PROJECT_SUMMARY               	ALDH4A1 are increased in mice and humans with atherosclerosis, supporting the
PR:PROJECT_SUMMARY               	potential use of ALDH4A1 as disease biomarker. A12 antibody infusion into
PR:PROJECT_SUMMARY               	LDLR-/- mice delayed plaque formation and reduced circulating levels of free
PR:PROJECT_SUMMARY               	cholesterol and LDL suggesting that anti-ALDH4A1 antibodies can play a
PR:PROJECT_SUMMARY               	protective role in atherosclerosis progression and might have therapeutic
PR:PROJECT_SUMMARY               	potential. Our study reveals a new auto-antigenic trigger target of the
PR:PROJECT_SUMMARY               	atherosclerosis-associated antibody response and opens new avenues for
PR:PROJECT_SUMMARY               	diagnostic and therapeutic interventions in CVD.
PR:INSTITUTE                     	Centro Nacional de Investigaciones Cardiovasculares Carlos III
PR:LAST_NAME                     	Ferrarini
PR:FIRST_NAME                    	Alessia
PR:ADDRESS                       	Calle de Melchor Fernández Almagro, 3, 28029 Madrid
PR:EMAIL                         	aferrarini@cnic.es
PR:PHONE                         	+34 914 53 12 00
#STUDY
ST:STUDY_TITLE                   	Untargeted lipidomics of liver to assess the potential protective role in
ST:STUDY_TITLE                   	atherosclerosis progression of A12 antibodies infusion into LDLR-/-mice
ST:STUDY_TYPE                    	LC-MS Untargeted Lipidomics
ST:STUDY_SUMMARY                 	In order to assess the therapeutic potential of A12 antibodies in
ST:STUDY_SUMMARY                 	atherosclerosis, untargeted lipidomics of liver samples was performed.
ST:STUDY_SUMMARY                 	LDLR-/-mice were treated with a fully murine version of the A12 antibody
ST:STUDY_SUMMARY                 	(mA12-IgG2b), with the isotype control antibody mB1.8-IgG2b (n=16) or with PBS
ST:STUDY_SUMMARY                 	as controls.
ST:INSTITUTE                     	Centro Nacional de Investigaciones Cardiovasculares Carlos III
ST:LAST_NAME                     	Ferrarini
ST:FIRST_NAME                    	Alessia
ST:ADDRESS                       	Calle de Melchor Fernández Almagro, 3, 28029 Madrid
ST:EMAIL                         	aferrarini@cnic.es
ST:PHONE                         	+34 914 53 12 00
ST:NUM_GROUPS                    	3
ST:TOTAL_SUBJECTS                	18
#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]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	A12_01	Antibody Group:A12	RAW_FILE_NAME=P_A12_01;N_A12_01
SUBJECT_SAMPLE_FACTORS           	-	A12_02	Antibody Group:A12	RAW_FILE_NAME=P_A12_02;N_A12_02
SUBJECT_SAMPLE_FACTORS           	-	A12_03	Antibody Group:A12	RAW_FILE_NAME=P_A12_03;N_A12_03
SUBJECT_SAMPLE_FACTORS           	-	A12_04	Antibody Group:A12	RAW_FILE_NAME=P_A12_04;N_A12_04
SUBJECT_SAMPLE_FACTORS           	-	A12_05	Antibody Group:A12	RAW_FILE_NAME=P_A12_05;N_A12_05
SUBJECT_SAMPLE_FACTORS           	-	A12_06	Antibody Group:A12	RAW_FILE_NAME=P_A12_06;N_A12_06
SUBJECT_SAMPLE_FACTORS           	-	B18_01	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_01;N_B18_01
SUBJECT_SAMPLE_FACTORS           	-	B18_02	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_02;N_B18_02
SUBJECT_SAMPLE_FACTORS           	-	B18_03	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_03;N_B18_03
SUBJECT_SAMPLE_FACTORS           	-	B18_04	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_04;N_B18_04
SUBJECT_SAMPLE_FACTORS           	-	B18_05	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_05;N_B18_05
SUBJECT_SAMPLE_FACTORS           	-	B18_06	Antibody Group:B1.8	RAW_FILE_NAME=P_B18_06;N_B18_06
SUBJECT_SAMPLE_FACTORS           	-	CTRL_01	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_01;N_CTRL_01
SUBJECT_SAMPLE_FACTORS           	-	CTRL_02	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_02;N_CTRL_02
SUBJECT_SAMPLE_FACTORS           	-	CTRL_03	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_03;N_CTRL_03
SUBJECT_SAMPLE_FACTORS           	-	CTRL_04	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_04;N_CTRL_04
SUBJECT_SAMPLE_FACTORS           	-	CTRL_05	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_05;N_CTRL_05
SUBJECT_SAMPLE_FACTORS           	-	CTRL_06	Antibody Group:PBS	RAW_FILE_NAME=P_CTRL_06;N_CTRL_06
SUBJECT_SAMPLE_FACTORS           	-	QC_01	Antibody Group:QC	RAW_FILE_NAME=P_QC_01;N_QC_01
SUBJECT_SAMPLE_FACTORS           	-	QC_02	Antibody Group:QC	RAW_FILE_NAME=P_QC_02;N_QC_02
SUBJECT_SAMPLE_FACTORS           	-	QC_03	Antibody Group:QC	RAW_FILE_NAME=P_QC_03;N_QC_03
SUBJECT_SAMPLE_FACTORS           	-	QC_04	Antibody Group:QC	RAW_FILE_NAME=P_QC_04;N_QC_04
SUBJECT_SAMPLE_FACTORS           	-	QC_05	Antibody Group:QC	RAW_FILE_NAME=P_QC_05;N_QC_05
SUBJECT_SAMPLE_FACTORS           	-	QC_06	Antibody Group:QC	RAW_FILE_NAME=P_QC_06;N_QC_06
SUBJECT_SAMPLE_FACTORS           	-	QC_07	Antibody Group:QC	RAW_FILE_NAME=P_QC_07;N_QC_07
#COLLECTION
CO:COLLECTION_SUMMARY            	Liver were collected after mice sacrifice, frozen in liquid N2 and store at
CO:COLLECTION_SUMMARY            	-80°C until the day of analysis.
CO:SAMPLE_TYPE                   	Liver
#TREATMENT
TR:TREATMENT_SUMMARY             	LDLR-/-mice under high fat diet were injected with mA12-IgG2b and PBS or a B1-8
TR:TREATMENT_SUMMARY             	IgG2b isotype as control antibody
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Frozen liver tissues were lysed in 0.5X PBS (sample:solvent 1:10 ratio)
SP:SAMPLEPREP_SUMMARY            	containing 1 mg/mL butylhydroxytoluene (BHT) solution in methanol (proportion
SP:SAMPLEPREP_SUMMARY            	200 µL per g of tissue), with FastPrep-24 5G instrument (MP Biomedicals, USA).
SP:SAMPLEPREP_SUMMARY            	25 µL aliquots of homogenate were collected and stored at -80°C until
SP:SAMPLEPREP_SUMMARY            	lipidomic extraction. Tissue homogenates were thawed and extracted with
SP:SAMPLEPREP_SUMMARY            	methyl-tert-butylether (MTBE) as described in [Matyash, V., et al., Lipid
SP:SAMPLEPREP_SUMMARY            	extraction by methyl-tert-butyl ether for high-throughput lipidomics. Journal of
SP:SAMPLEPREP_SUMMARY            	lipid research, 2008. 49(5): p. 1137-46]. 900 µL of organic phase were
SP:SAMPLEPREP_SUMMARY            	dried-out in speedvac and resuspended in 50 µL of ACN:H2O (20:80, v:v) just
SP:SAMPLEPREP_SUMMARY            	before injection.
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	Reversed phase
CH:INSTRUMENT_NAME               	Thermo Dionex Ultimate 3000
CH:COLUMN_NAME                   	Agilent mRP-Recovery C18 column (100 × 0.5 mm, 5 µm)
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Thermo Orbitrap Elite Hybrid Ion Trap-Orbitrap
MS:INSTRUMENT_TYPE               	Orbitrap
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:MS_COMMENTS                   	MS was operating in full scan mode from 70 to 1700 m/z at 60000 resolution. Data
MS:MS_COMMENTS                   	processing was carried-out using Compound Discoverer (ThermoFisher; USA) with
MS:MS_COMMENTS                   	the Metaboprofiler node.
MS:MS_RESULTS_FILE               	ST001434_AN002397_Results.txt	UNITS:peak area	Has m/z:Yes	Has RT:No	RT units:No RT data
#END