scholarly journals Long-term protein exposure reduces albumin binding and uptake in proximal tubule-derived opossum kidney cells.

1998 ◽  
Vol 9 (6) ◽  
pp. 960-968 ◽  
Author(s):  
M Gekle ◽  
S Mildenberger ◽  
R Freudinger ◽  
S Silbernagl
Keyword(s):  
Amino Acids ◽  
Proximal Tubule ◽  
Uptake Rate ◽  
Kidney Cells ◽  
Proximal Tubular Cells ◽  
Opossum Kidney ◽  
Tubular Cells ◽  
Opossum Kidney Cells ◽  
Proximal Tubular ◽  
Protein Reabsorption

To avoid renal loss of large amounts of proteins, filtered proteins are reabsorbed by endocytosis along the proximal tubule. However, although protein reabsorption is a task of proximal tubular cells, it is also a threat because it may cause cell injury. This study determines whether exposure to bovine serum albumin (BSA) leads to regulatory changes in endocytosis of FITC-BSA in proximal tubule-derived opossum kidney cells. Preincubation with BSA led to a decrease of FITC-BSA endocytosis with an IC50 value of 0.58 g/L. Specific binding of FITC-BSA to the apical membrane was also reduced (IC50 = 0.69 g/L). Kinetic analyses revealed that maximal uptake rate and maximal binding capacity were decreased with no change in affinity. Similar effects were observed after preincubation with equimolar amounts of other proteins (lactalbumin, transferrin, and conalbumin), but not after preincubation with dextran. The effect of preincubation with BSA could be mimicked by preincubation with some amino acids. Preincubation with L-Ala, L-Gln, or NH4Cl, but not with L-Leu, L-Glu, or L-Asp, reduced FITC-BSA endocytosis and binding. Preincubation with BSA, but not with dextran, reduced protein degradation and increased ammonia production, vesicular pH, as well as the rate of lactate dehydrogenase release. Apical fluid-phase endocytosis and apical uptake of neutral amino acids were not reduced. It is concluded that proximal tubular cells reduce the uptake rate for proteins, but not for other substrates, in response to increased protein load. This reduction is achieved by reducing the number of apical binding sites, partially in response to increased ammoniagenesis with deranged vesicular pH and enzyme activities. Thus, increased protein filtration could result in reduced protein reabsorption, thereby enhancing proteinuria.

CD36 mediates proximal tubular binding and uptake of albumin and is upregulated in proteinuric nephropathies

2012 ◽  
Vol 303 (7) ◽  
pp. F1006-F1014 ◽  
Author(s):  
Richard J. Baines ◽  
Ravinder S. Chana ◽  
Matthew Hall ◽  
Maria Febbraio ◽  
David Kennedy ◽  
...  
Keyword(s):  
Proximal Tubule ◽  
Renal Biopsy ◽  
Renal Diseases ◽  
Creatinine Ratio ◽  
Proximal Tubular Cells ◽  
Opossum Kidney ◽  
Tubular Cells ◽  
Proximal Tubular

Dysregulation of renal tubular protein handling in proteinuria contributes to the development of chronic kidney disease. We investigated the role of CD36 as a novel candidate mediator of albumin binding and endocytosis in the kidney proximal tubule using both in vitro and in vivo approaches, and in nephrotic patient renal biopsy samples. In CD36-transfected opossum kidney proximal tubular cells, both binding and uptake of albumin were substantially enhanced. A specific CD36 inhibitor abrogated this effect, but receptor-associated protein, which blocks megalin-mediated endocytosis of albumin, did not. Mouse proximal tubular cells expressed CD36 and this was absent in CD36 null animals, whereas expression of megalin was equal in these animals. Compared with wild-type mice, CD36 null mice demonstrated a significantly increased urinary protein-to-creatinine ratio and albumin-to-creatinine ratio. Proximal tubular cells expressed increased CD36 when exposed to elevated albumin concentrations in culture medium. Expression of CD36 was studied in renal biopsy tissue obtained from adult patients with heavy proteinuria due to minimal change disease, membranous nephropathy, or focal segmental glomerulosclerosis. Proximal tubular CD36 expression was markedly increased in proteinuric individuals. We conclude that CD36 is a novel mediator influencing binding and uptake of albumin in the proximal tubule that is upregulated in proteinuric renal diseases. CD36 may represent a potential therapeutic target in proteinuric nephropathy.

scholarly journals Na+/Pi co-transport alters rapidly cytoskeletal protein polymerization dynamics in opossum kidney cells

1996 ◽  
Vol 315 (1) ◽  
pp. 241-247 ◽  
Author(s):  
Evangelia A. PAPAKONSTANTI ◽  
Dimitrios S. EMMANOUEL ◽  
Achille GRAVANIS ◽  
Christos STOURNARAS
Keyword(s):  
Immunoblot Analysis ◽  
Kidney Cells ◽  
Opossum Kidney ◽  
Protein Polymerization ◽  
Phosphonoformic Acid ◽  
Opossum Kidney Cells ◽  
Proximal Tubular ◽  
Microtubule Stabilizer ◽  
Dynamic Equilibria ◽  
Contrast Measurement

We studied with biochemical and immunofluorescent techniques the interactions between the actin microfilament and tubulin microtubule cytoskeleton and Na+/Pi co-transport in opossum kidney cells, a line with proximal tubular characteristics. On brief (5 min) incubation of the cells with a low (0.1 mM) concentration of Pi, a rapid F-actin depolymerization takes place, which fails to occur in cells incubated under similar conditions with 1 mM Pi. The disassembly of actin microfilaments could be quantitatively expressed as a 33% increase in the ratio of monomeric G-actin to polymerized F-actin (G/F-actin ratio from 0.80±0.03 to 1.06±0.06, n = 28, P < 0.01), owing to a significant decrease in the latter. Under these conditions microfilaments were also markedly destabilized, as shown by their diminished resistance to graded cytochalasin B concentrations. In addition, incubation of opossum kidney cells with low Pi concentrations (0.1 mM) resulted within 5 min in a substantial depolymerization of microtubules, shown by immunofluorescence microscopy and measured as a 70.9±6.9% (n = 11, P < 0.01) decrement by immunoblot analysis. These changes, which occur only when extracellular Pi concentrations are kept low, seem to be related to a significant increase within 5 min in the rate of cellular Pi uptake by 25.5% under these conditions. The shifts in the dynamic equilibria between monomeric and polymerized actin and tubulin in response to cellular Pi uptake were transient, being fully reversible within 30 min. Moreover, the effect of Pi seemed to be specific because inhibition of its uptake by phosphonoformic acid blunted microtubular disassembly markedly. In contrast, measurement of Pi uptake in the presence of agents known to stabilize cytoskeletal structures showed a substantial decrease with phallacidin, which stabilizes microfilaments, whereas the microtubule stabilizer taxol had no apparent effect. These results indicate that acute alterations in the polymerization dynamics and stability of both microfilaments and microtubules are involved in the modulation of Na+/Pi co-transport and suggest important cytoskeletal participation in proximal tubular transport functions.

The effect of 2,3,4-trimethylpentane on the ultrastructure of proximal tubular cells in primary cell culture

1989 ◽  
Vol 47 ◽  
pp. 1090-1091
Author(s):  
D.R. Mattie ◽  
J.J. Maslanka ◽  
N.J. Del Raso ◽  
M.R. Chase
Keyword(s):  
Proximal Tubule ◽  
Male Rat ◽  
Proximal Tubular Cells ◽  
Thin Sections ◽  
Proximal Tubule Cells ◽  
Tubular Cells ◽  
Transmission Electron ◽  
Cacodylate Buffer ◽  
Proximal Tubular ◽  
Tubule Cells

To aid in the assessment of the risk of Air Force personnel working with hydrocarbon fuels and compounds, an attempt was made to further characterize the nephropathy that results from exposure to hydrocarbons. The purpose of this study was to isolate and establish purified primary cultures of male rat proximal tubular cells suitable for experimental exposure to sublethal concentrations of solubilized 2,3, 4-trimethylpentane (TMP), a model hydrocarbon. Experiments were conducted to evaluate the cytotoxicity and metabolism of solubilized TMP in media containing or lacking the protein albumin.Proximal tubule cells in primary suspension culture were exposed to one of the following levels of TMP: 7.9, 12.0, 15.7, 19.1 or 25.5 mM. After 4 hours of exposure, pelleted cells were fixed for transmission electron microscopy by resuspension in 2% glutaraldehyde and 2.5% paraformaldehyde in 0.1M cacodylate buffer at pH 7.4. After a minimum fixation of at least 24 hours, the cells were post-fixed with 2% osmium tetroxide in 0,1M cacodylate buffer at pH 7.4. Cells were processed into Polybed 812 plastic capsules. Sections one micron thick, were cut in order to verify that cells were intact and suitable for thin sectioning. Thin sections (60- 90 nm) were cut on an ultramicrotome using a diamond knife. Thin sections, stained with uranyl acetate and lead citrate, were examined with a transmission electron microscope at 60 kV. Photographs of representative proximal tubule cells were taken at three levels of magnification.

scholarly journals Apoptosis as a mechanism of the albumin-induced kidney damage in childhood nephrotic syndrome

2018 ◽  
pp. 25-30
Author(s):  
Ie.A. Burlaka ◽  
I.V. Bagdasarova
Keyword(s):  
Nephrotic Syndrome ◽  
Primary Culture ◽  
Kidney Damage ◽  
In Vitro Studies ◽  
Kidney Cells ◽  
Proximal Tubular Cells ◽  
Tubular Cells ◽  
Proximal Tubular ◽  
Nephrotic Children

It was shown previously on in vivo studies that proteinuria-induced effects play a crucial role in renal damage in chronic kidney disease (CKD). However, an initial mechanism of irreversible kidney damage in pediatric diseases characterized by chronic proteinuria, i.e. nephrotic syndrome, remains to be unclear. The aim of our work was to study the initial mechanism of kidney cells apoptosis development in nephrotic children. Methods.An examination of renal biopsies of 53 patients (aged 10 to 15 years) with nephrotic syndrome hospitalized in Pediatric Nephrology unit of the Children Clinical Hospital №7 (Kyiv, Ukraine) done. In vitro studies of albumin toxicity performed on rat proximal tubular cells in primary culture (RPTC). Results. Our study showed that albumin overload in nephrotic children leads to high levels of apoptosis. Its distribution and level varies regarding the level of focal segmental glomerulosclerosis (FSGS). The progression of sclerosis as a sign of irreversible kidney damage is accompanied by gradual increase in expression of proapoptotic factor Bax. In vitro studies on rat proximal tubular cells in primary culture (RPTC) showed that excessive albumin uptake into rat primary renal cells causes an almost immediate mitochondrial accumulation of the apoptotic factor Bax. We hypothesize that this might be initial pathway leading to kidney cells apoptosis in childhood nephrotic syndrome. Conclusions. We show thatoverexpression of apoptotic factor Bax has a place in children with nephrotic syndrome. Thus, chronic influence of albumin is a factor predisposing disturbances in system controlling apoptosis in this cohort of patients. Our data demonstrate that there is a dependence between the Bax overexpression level and the stage of CKD. We show the topologic difference between the Bax levels and FSGS degree. This is an indication thatdevelopment of glomerular and tubule-interstitial disorders under the influence of proteinuria occurs in specific range. In vitro data demonstrate that albumin overload causes mitochondrial Bax translocation that could be an initial factor in apoptotic pathway activation.

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