1989
DOI: 10.1002/jcp.1041410128
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Maintenance of proximal and distal cell functions in SV40‐transformed tubular cell lines derived from rabbit kidney cortex

Abstract: This paper reports the preparation and describes the properties of three renal tubular cell lines derived using SV40 infection of primary cultures of rabbit kidney cortical cells, enriched in proximal cells. RC.SV1 was initially derived from cultures grown in the presence of fetal calf serum exhibiting a low degree of proximal differentiation. The cells were subsequently adapted to grow in serum-free hormonally defined medium and display basic properties of proximal tubule cells including well-developed apical… Show more

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Cited by 76 publications
(57 citation statements)
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“…Briefly, the kidneys were rapidly removed under sterile conditions, and primary cultures of RTECs were prepared using previously described methods (8,33). Kidneys were injected using fine needles with modified defined medium (DM) as described (33) supplemented with 0.1% collagenase (Roche Diagnostics GmBH).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Briefly, the kidneys were rapidly removed under sterile conditions, and primary cultures of RTECs were prepared using previously described methods (8,33). Kidneys were injected using fine needles with modified defined medium (DM) as described (33) supplemented with 0.1% collagenase (Roche Diagnostics GmBH).…”
Section: Methodsmentioning
confidence: 99%
“…Thin kidney slices were then minced and incubated in the same collagenase-supplemented DM for 45 min at 37°C. Kidney slices were gently dispersed using sterile needles, and then poured through 100-and 40-m nylon gauzes, as described (33). The resulting cell suspension was then seeded on chambered coverglass slides or collagencoated 48-well trays (ϳ 2 ϫ 10 4 cells per well), and grown at 37°C in a 5% CO 2 -95% air atmosphere in the same modified defined DM medium.…”
Section: Methodsmentioning
confidence: 99%
“…To analyze the effects of temperature per se irrespective of the functional status of SV40 large-T oncogene on metalloproteinase synthesis, we used as control a rabbit collecting duct cell line of the same cell type origin (RC.SV3), previously established in our laboratory after infection of renal cells with the wild-type SV40 strain LP (23). This cell line was studied under the same culture conditions as RC.SVtsA58 and analyzed at 33 and 39.5°C.…”
Section: Methodsmentioning
confidence: 99%
“…Rabbit RCSV3 cells derived from a kidney cortical collecting duct 14 (kindly provided by Prof P. Ronco, Hôpital Tenon, Paris, France) were grown as described previously 15 and transfected using lipofectamine 2000 (Invitrogen) with 0.25 g of pcDNA3 plasmid containing either MR-2G or MR-2C, 0.625 g of a GRE2_TATA_luc reporter plasmid plasmid 16 and 0.25 g of pSV␤gal. The day after transfection, steroids were added at different concentrations, and 48 hours after transfection, luciferase and ␤-galactosidase activities were assayed using the Dual-Light System and the Galacton-Plus Substrate (Applied Biosystems).…”
Section: Transactivation Assaysmentioning
confidence: 99%