Results 41 to 48 of about 13,206,578 (48)
Cyclosporine A-induced toxicity in two renal cell culture models (LLC-PK1 and MDCK)
Renal damage caused by therapeutic treatment with cyclosporine A has been well documented. Clinical experiences have shown that cyclosporine A nephrotoxicity is determined by interstitial fibrosis with tubular atrophy.
R. Rezzani +4 more
core +2 more sources
In LLC-PK1 porcine epithelial cells, the urokinase-type plasminogen activator (u-PA) mRNA and protein can be induced either by stimulation of the protein kinase C (PKC) pathway using a tumor promoter (PMA) or by stimulation of the protein kinase A (PKA ...
Knesel J +6 more
core +1 more source
Induction of mitochondrial metabolism and pH-modulated ammoniagenesis by rocking LLC-PK1 cells
In an effort to find a model system in which the regulation of renal ammoniagenesis could be delineated, the LLC-PK1 line of cultured pig kidney epithelial cells was examined.
J. M. Scheid, L. A. Cole, R. L. Tannen
core +1 more source
cDNA cloning and immunolocalization of a Na(+)-H+ exchanger in LLC-PK1 renal epithelial cells
LLC-PK1 cells, an established line from pig kidney, express basolateral and apical Na(+)-H+ exchangers that can be distinguished by their different sensitivities to the amiloride analogue, N-ethyl-N-isopropylamiloride.
C. Sardet +7 more
core +1 more source
An antibody to plasminogen activator (PA) produced by the cultured cells of the pig kidney cell strain LLC-PK1 (LP100) was used to localize PA on the cell's free (unattached) surface. Localization was accomplished by the unlabeled antibody enzyme method
D C Paul +3 more
core +1 more source
The LLC-PK1 mutant cell lines FIB4 and FIB6 are affected in the catalytic (C) subunit of cAMP-dependent protein kinase (cAMP-PK) such that they possess less than 10% parental activity.
Botterell SH, Hemmings BA, Jans DA
core +1 more source
PDI effects on cGMP generation of LLC-PK1 cells stimulated by ANP.
A. PDI expression in vascular smooth muscle cells (VSMC), endothelial cells (HUVEC), and mesangial cells (HMC). Expression of PDI was not detected on LLC-PK1 cells (porcine renal tubular cells). B.
John C. Burnett Jr (282938) +7 more
core +1 more source
GRP78/BIP is Involved in Ouabain-Induced Endocytosis of the Na/K-ATPase in LLC-PK1 Cells
We have demonstrated that ouabain causes dose- and time-dependent decreases both in 86Rb+ uptake and plasmalemmal Na/K-ATPase content of LLC-PK1 cells, which is related to ouabain-induced endocytosis of plasmalemmal Na/K-ATPase in LLC-PK1 cells through a
Liu, Jiang, Kesiry, Riad
core

