Smoking exposure induces human lung endothelial cell adaptation to apoptotic stress

American Journal of Respiratory Cell and Molecular Biology

Volumn 50, Issue 3, 2014, Pages 513-525

  Petrusca, Daniela N ^a   Van Demark, Mary ^a   Gu, Yuan ^a   Justice, Matthew J ^a   Rogozea, Adriana ^a   Hubbard, Walter C ^c   Petrache, Irina ^a,b  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b RICHARD L ROUDEBUSH VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Apoptosis; Autophagy; Chronic obstructive pulmonary disease; High mobility group box 1; Sphingolipids

Indexed keywords

APOPTOSIS INDUCING FACTOR; CASPASE; CASPASE 3; CERAMIDE; MICROTUBULE ASSOCIATED PROTEIN 1; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE;

APOPTOSIS; ARTICLE; AUTOPHAGY; CELL DIVISION; CELL PROLIFERATION; CELL STRESS; CELL SURVIVAL; CELL VIABILITY; CHRONIC OBSTRUCTIVE LUNG DISEASE; CONTROLLED STUDY; DEPOLARIZATION; ENDOPLASMIC RETICULUM STRESS; ENDOTHELIUM CELL; HUMAN; HUMAN CELL; LONG TERM EXPOSURE; LUNG ALVEOLUS CELL; MITOCHONDRIAL MEMBRANE; PHOSPHORYLATION; PROTEIN EXPRESSION; PROTEIN INDUCTION; SMOKING; UPREGULATION;

ADAPTATION, PHYSIOLOGICAL; APOPTOSIS; APOPTOSIS REGULATORY PROTEINS; AUTOPHAGY; CELL PROLIFERATION; CELLS, CULTURED; CERAMIDES; DOSE-RESPONSE RELATIONSHIP, DRUG; ENDOTHELIAL CELLS; HMGB1 PROTEIN; HUMANS; LUNG; MEMBRANE POTENTIAL, MITOCHONDRIAL; PALMITIC ACIDS; PARACRINE COMMUNICATION; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-AKT; SIGNAL TRANSDUCTION; SMOKE; SMOKING; STRESS, PHYSIOLOGICAL; TIME FACTORS;

EID: 84895543498     PISSN: 10441549     EISSN: 15354989     Source Type: Journal    
DOI: 10.1165/rcmb.2013-0023OC     Document Type: Article

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