#METABOLOMICS WORKBENCH  DATATRACK_ID:4082 STUDY_ID:ST000275 ANALYSIS_ID:AN000439
VERSION                          	1
CREATED_ON                       	08-09-2023
#PROJECT
PR:PROJECT_TITLE                 	Metabolic analysis of Parp1 ko/wt Saline & Bleo Mouse Lung Fibroblasts and Human
PR:PROJECT_TITLE                 	IPF & Normal Lung Fibroblasts
PR:PROJECT_TYPE                  	Glycolysis/TCA/Nucleotide analysis (tissue/cells)
PR:PROJECT_SUMMARY               	Hedgehog signaling plays important roles in cell development and
PR:PROJECT_SUMMARY               	differentiation. In this study, the ability of Sonic Hedgehog (SHH) to induce
PR:PROJECT_SUMMARY               	myofibroblast differentiation was analyzed in isolated human lung fibroblasts,
PR:PROJECT_SUMMARY               	and its in vivo significance was evaluated in rodent bleomycin-induced pulmonary
PR:PROJECT_SUMMARY               	fibrosis. The results showed that SHH could induce myofibroblast differentiation
PR:PROJECT_SUMMARY               	in human lung fibroblasts in a Smo- and Gli1-dependent manner. Gel shift
PR:PROJECT_SUMMARY               	analysis, chromatin immunoprecipitation assay, and site-directed mutagenesis
PR:PROJECT_SUMMARY               	revealed that a Gli1 binding consensus in the ?-SMA gene promoter was important
PR:PROJECT_SUMMARY               	for mediating SHH-induced myofibroblast differentiation. Analysis of Hedgehog
PR:PROJECT_SUMMARY               	reemergence in vivo revealed that of all three Hedgehog isoforms, only SHH was
PR:PROJECT_SUMMARY               	significantly induced in bleomycin-injured lung along with Gli1. The induction
PR:PROJECT_SUMMARY               	of SHH was only noted in epithelial cells, and its expression was undetectable
PR:PROJECT_SUMMARY               	in lung fibroblasts or macrophages. Transforming growth factor (TGF)-? induced
PR:PROJECT_SUMMARY               	SHH significantly in cultured alveolar epithelial cells, whereas SHH induced
PR:PROJECT_SUMMARY               	TGF-? in lung fibroblasts. Pulmonary fibrosis and ?-smooth muscle actin (?-SMA)
PR:PROJECT_SUMMARY               	expression were significantly reduced in mice that were Smo deficient only in
PR:PROJECT_SUMMARY               	type I collagen–expressing cells. Thus, the reemergence of SHH in epithelial
PR:PROJECT_SUMMARY               	cells could result in induction of myofibroblast differentiation in a
PR:PROJECT_SUMMARY               	Smo-dependent manner and subsequent Gli1 activation of the ?-SMA promoter.
PR:INSTITUTE                     	University of Michigan
PR:DEPARTMENT                    	Deaprtment of Pathology
PR:LABORATORY                    	Sem H. Phan
PR:LAST_NAME                     	Hu
PR:FIRST_NAME                    	Biao
PR:ADDRESS                       	Ann Arbor, MI
PR:EMAIL                         	biaohu@med.umich.edu
PR:PHONE                         	734-7635731
PR:DOI                           	http://dx.doi.org/10.21228/M8359Z
#STUDY
ST:STUDY_TITLE                   	Metabolic analysis of Parp1 ko/wt Saline & Bleo Mouse Lung Fiboblasts and Human
ST:STUDY_TITLE                   	IPF & Normal Lung Fiboblasts (Part 2)
ST:STUDY_TYPE                    	Glycolysis/TCA/Nucleotide analysis. Ceramide analysis for parp1 wild type lung
ST:STUDY_TYPE                    	tissue/Cells after saline or bleomycin treatment.
ST:STUDY_SUMMARY                 	This study is a part of series performed for the same researcher through
ST:STUDY_SUMMARY                 	pilot/feasibility grant program, so the publication is relevant reference for
ST:STUDY_SUMMARY                 	other studies (ST000143, ST000183) This specific experiment is a small pilot
ST:STUDY_SUMMARY                 	study to establish method performance, it includes four biological replicas of
ST:STUDY_SUMMARY                 	identical cell cultures after the identical treatment and a single tissue
ST:STUDY_SUMMARY                 	sample.
ST:INSTITUTE                     	University of Michigan
ST:DEPARTMENT                    	Deaprtment of Pathology
ST:LABORATORY                    	Sem H. Phan
ST:LAST_NAME                     	Hu
ST:FIRST_NAME                    	Biao
ST:ADDRESS                       	Ann Arbor, MI
ST:EMAIL                         	biaohu@med.umich.edu
ST:PHONE                         	734-7635731
ST:SUBMIT_DATE                   	2014-06-11
#SUBJECT
SU:SUBJECT_TYPE                  	Animal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
SU:SPECIES_GROUP                 	Mammal
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	S00014994	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00014995	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00014996	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00014997	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00014998	Sample type:Tissue | Genetic background:B6 wt | bleomycin:yes	
#COLLECTION
CO:COLLECTION_SUMMARY            	-
CO:SAMPLE_TYPE                   	Cells
#TREATMENT
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	-
SP:SAMPLEPREP_PROTOCOL_FILENAME  	Gly-TCA-nucleotides_analysis_protocol-2015-03-09.docx
#CHROMATOGRAPHY
CH:METHODS_ID                    	AQM020
CH:METHODS_FILENAME              	QTOF-002-HILIC-35min-1mm.m
CH:INSTRUMENT_NAME               	Agilent 1260
CH:COLUMN_NAME                   	Phenomenex Luna NH2 (150 x 1mm,3um)
CH:CHROMATOGRAPHY_TYPE           	HILIC
#ANALYSIS
AN:LABORATORY_NAME               	MRC2 (University of Michigan)
AN:ANALYSIS_TYPE                 	MS
AN:ACQUISITION_ID                	AQM011
AN:ACQUISITION_PARAMETERS_FILE   	ALPHA_KETO_ACIDS-FULL.M
AN:PROCESSING_PARAMETERS_FILE    	EX00310-MassHunterQuant-GlyTCA-DataAnalysis-GCMS-Method.m
#MS
MS:INSTRUMENT_NAME               	Agilent 6530 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	uM (500ul of extraction solvent)
MS_METABOLITE_DATA_START
Samples	S00014994	S00014995	S00014996	S00014997	S00014998
Factors	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	Sample type:Cell culture | Genetic background:B6 wt | bleomycin:yes	Sample type:Tissue | Genetic background:B6 wt | bleomycin:yes	
Alanine	6.2436	5.8979	6.0826	5.8632	4.4470
alpha-Ketoglutarate	0.3880	0.3836	0.4108	0.4049	0.2233
Aspartate	7.7196	7.1164	8.4866	7.9883	17.3353
fumarate	0.5219	0.5178	0.5209	0.5249	0.5905
Glutamate	8.6397	7.9679	8.8075	8.5750	4.3956
glutamine	12.1172	10.6305	12.8258	14.2882	3.0844
Lactate	30.9503	39.2068	32.3482	43.0763	10.2946
Oxaloacetate					
pyruvate	2.0451	2.3407	2.0106	2.4476	1.1894
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	
Alanine	5950		C00041	ALA	UM_Target_ID				
alpha-Ketoglutarate	51		C00026	AKG	UM_Target_ID				
Aspartate	5960		C00049	ASP	UM_Target_ID				
fumarate	444972		C00122	FUM	UM_Target_ID				
Glutamate	611			GLU	UM_Target_ID				
glutamine	5961		C00064	GLN	UM_Target_ID				
Lactate	107689		C00186	LAC	UM_Target_ID				
Oxaloacetate	970		C00036	OAA	UM_Target_ID				
pyruvate	1060		C00022	PYR	UM_Target_ID				
METABOLITES_END
#END