Papilloma virus immortalized tracheal epithelial cells retain a well-differentiated phenotype. 1993

J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
Division of Pulmonary Diseases, University of North Carolina, Chapel Hill 27599.

Human airway epithelial cell lines that retain phenotypic properties representative of the native tissue will be useful physiological models. Human papilloma viral (HPV) genes can immortalize human genital keratinocytes and breast and bronchial epithelia. We transfected cystic fibrosis (CF) and normal tracheobronchial epithelial cell cultures with DNA encoding the HPV-18 E6 and E7 genes and characterized phenotypic properties of resultant cell lines. Of the 11 CF clones isolated, 6 developed a polarized phenotype with vectorial ion transport and membrane-specific expression of histamine and purinergic receptors. The ion transport properties of these lines differed from the normal lines and approximated those of primary CF airway epithelial cell cultures more closely than do those of cell lines transformed with the simian virus 40 large T gene. When transplanted into denuded tracheal grafts, these cells can differentiate into ciliated and secretory phenotypes. We conclude that HPV-18 E6 and E7 genes are sufficient to transform human airway epithelial cells and that the resultant cell lines express differentiated phenotypic properties that approximate those of the native epithelium.

UI MeSH Term Description Entries
D008297 Male Males
D008564 Membrane Potentials The voltage differences across a membrane. For cellular membranes they are computed by subtracting the voltage measured outside the membrane from the voltage measured inside the membrane. They result from differences of inside versus outside concentration of potassium, sodium, chloride, and other ions across cells' or ORGANELLES membranes. For excitable cells, the resting membrane potentials range between -30 and -100 millivolts. Physical, chemical, or electrical stimuli can make a membrane potential more negative (hyperpolarization), or less negative (depolarization). Resting Potentials,Transmembrane Potentials,Delta Psi,Resting Membrane Potential,Transmembrane Electrical Potential Difference,Transmembrane Potential Difference,Difference, Transmembrane Potential,Differences, Transmembrane Potential,Membrane Potential,Membrane Potential, Resting,Membrane Potentials, Resting,Potential Difference, Transmembrane,Potential Differences, Transmembrane,Potential, Membrane,Potential, Resting,Potential, Transmembrane,Potentials, Membrane,Potentials, Resting,Potentials, Transmembrane,Resting Membrane Potentials,Resting Potential,Transmembrane Potential,Transmembrane Potential Differences
D008565 Membrane Proteins Proteins which are found in membranes including cellular and intracellular membranes. They consist of two types, peripheral and integral proteins. They include most membrane-associated enzymes, antigenic proteins, transport proteins, and drug, hormone, and lectin receptors. Cell Membrane Protein,Cell Membrane Proteins,Cell Surface Protein,Cell Surface Proteins,Integral Membrane Proteins,Membrane-Associated Protein,Surface Protein,Surface Proteins,Integral Membrane Protein,Membrane Protein,Membrane-Associated Proteins,Membrane Associated Protein,Membrane Associated Proteins,Membrane Protein, Cell,Membrane Protein, Integral,Membrane Proteins, Integral,Protein, Cell Membrane,Protein, Cell Surface,Protein, Integral Membrane,Protein, Membrane,Protein, Membrane-Associated,Protein, Surface,Proteins, Cell Membrane,Proteins, Cell Surface,Proteins, Integral Membrane,Proteins, Membrane,Proteins, Membrane-Associated,Proteins, Surface,Surface Protein, Cell
D009856 Oncogene Proteins, Viral Products of viral oncogenes, most commonly retroviral oncogenes. They usually have transforming and often protein kinase activities. Viral Oncogene Proteins,Viral Transforming Proteins,v-onc Proteins,Transforming Proteins, Viral,v onc Proteins
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D011916 Rats, Inbred F344 An inbred strain of rat that is used for general BIOMEDICAL RESEARCH purposes. Fischer Rats,Rats, Inbred CDF,Rats, Inbred Fischer 344,Rats, F344,Rats, Inbred Fisher 344,CDF Rat, Inbred,CDF Rats, Inbred,F344 Rat,F344 Rat, Inbred,F344 Rats,F344 Rats, Inbred,Inbred CDF Rat,Inbred CDF Rats,Inbred F344 Rat,Inbred F344 Rats,Rat, F344,Rat, Inbred CDF,Rat, Inbred F344,Rats, Fischer
D001920 Bradykinin A nonapeptide messenger that is enzymatically produced from KALLIDIN in the blood where it is a potent but short-lived agent of arteriolar dilation and increased capillary permeability. Bradykinin is also released from MAST CELLS during asthma attacks, from gut walls as a gastrointestinal vasodilator, from damaged tissues as a pain signal, and may be a neurotransmitter. Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg,Bradykinin Acetate, (9-D-Arg)-Isomer,Bradykinin Diacetate,Bradykinin Hydrochloride,Bradykinin Triacetate,Bradykinin, (1-D-Arg)-Isomer,Bradykinin, (2-D-Pro)-Isomer,Bradykinin, (2-D-Pro-3-D-Pro-7-D-Pro)-Isomer,Bradykinin, (2-D-Pro-7-D-Pro)-Isomer,Bradykinin, (3-D-Pro)-Isomer,Bradykinin, (3-D-Pro-7-D-Pro)-Isomer,Bradykinin, (5-D-Phe)-Isomer,Bradykinin, (5-D-Phe-8-D-Phe)-Isomer,Bradykinin, (6-D-Ser)-Isomer,Bradykinin, (7-D-Pro)-Isomer,Bradykinin, (8-D-Phe)-Isomer,Bradykinin, (9-D-Arg)-Isomer,Arg Pro Pro Gly Phe Ser Pro Phe Arg
D002118 Calcium A basic element found in nearly all tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes. Coagulation Factor IV,Factor IV,Blood Coagulation Factor IV,Calcium-40,Calcium 40,Factor IV, Coagulation
D002217 Carbachol A slowly hydrolyzed CHOLINERGIC AGONIST that acts at both MUSCARINIC RECEPTORS and NICOTINIC RECEPTORS. Carbamylcholine,Carbacholine,Carbamann,Carbamoylcholine,Carbastat,Carbocholine,Carboptic,Doryl,Isopto Carbachol,Jestryl,Miostat,Carbachol, Isopto
D002454 Cell Differentiation Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs. Differentiation, Cell,Cell Differentiations,Differentiations, Cell

Related Publications

J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
June 2020, Heliyon,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
October 1992, Genes, chromosomes & cancer,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
January 1995, Critical reviews in oncogenesis,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
December 1994, Glycobiology,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
November 2010, Journal of virology,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
January 2008, Experimental cell research,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
May 2004, Journal of veterinary medicine. A, Physiology, pathology, clinical medicine,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
January 2004, In vitro cellular & developmental biology. Animal,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
January 2018, International journal of cell biology,
J R Yankaskas, and J E Haizlip, and M Conrad, and D Koval, and E Lazarowski, and A M Paradiso, and C A Rinehart, and B Sarkadi, and R Schlegel, and R C Boucher
July 1993, The American journal of physiology,
Copied contents to your clipboard!