Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells
Autor(a) principal: | |
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Data de Publicação: | 2000 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0100-879X2000000100015 http://repositorio.unifesp.br/handle/11600/882 |
Resumo: | Calcium oxalate (CaOx) crystals adhere to and are internalized by tubular renal cells and it seems that this interaction is related (positively or negatively) to the appearance of urinary calculi. The present study analyzes a series of mechanisms possibly involved in CaOx uptake by Madin-Darby canine kidney (MDCK) cells. CaOx crystals were added to MDCK cell cultures and endocytosis was evaluated by polarized light microscopy. This process was inhibited by an increase in intracellular calcium by means of ionomycin (100 nM; N = 6; 43.9% inhibition; P<0.001) or thapsigargin (1 µM; N = 6; 33.3% inhibition; P<0.005) administration, and via blockade of cytoskeleton assembly by the addition of colchicine (10 µM; N = 8; 46.1% inhibition; P<0.001) or cytochalasin B (10 µM; N = 8; 34.2% inhibition; P<0.001). Furthermore, CaOx uptake was reduced when the activity of protein kinase C was inhibited by staurosporine (10 nM; N = 6; 44% inhibition; P<0.01), or that of cyclo-oxygenase by indomethacin (3 µM; N = 12; 17.2% inhibition; P<0.05); however, the uptake was unaffected by modulation of potassium channel activity with glibenclamide (3 µM; N = 6), tetraethylammonium (1 mM; N = 6) or cromakalim (1 µM; N = 6). Taken together, these data indicate that the process of CaOx internalization by renal tubular cells is similar to the endocytosis reported for other systems. These findings may be relevant to cellular phenomena involved in early stages of the formation of renal stones. |
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Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cellscalcium oxalateDCK cellsmechanisms of endocytosisrenal stoneCalcium oxalate (CaOx) crystals adhere to and are internalized by tubular renal cells and it seems that this interaction is related (positively or negatively) to the appearance of urinary calculi. The present study analyzes a series of mechanisms possibly involved in CaOx uptake by Madin-Darby canine kidney (MDCK) cells. CaOx crystals were added to MDCK cell cultures and endocytosis was evaluated by polarized light microscopy. This process was inhibited by an increase in intracellular calcium by means of ionomycin (100 nM; N = 6; 43.9% inhibition; P<0.001) or thapsigargin (1 µM; N = 6; 33.3% inhibition; P<0.005) administration, and via blockade of cytoskeleton assembly by the addition of colchicine (10 µM; N = 8; 46.1% inhibition; P<0.001) or cytochalasin B (10 µM; N = 8; 34.2% inhibition; P<0.001). Furthermore, CaOx uptake was reduced when the activity of protein kinase C was inhibited by staurosporine (10 nM; N = 6; 44% inhibition; P<0.01), or that of cyclo-oxygenase by indomethacin (3 µM; N = 12; 17.2% inhibition; P<0.05); however, the uptake was unaffected by modulation of potassium channel activity with glibenclamide (3 µM; N = 6), tetraethylammonium (1 mM; N = 6) or cromakalim (1 µM; N = 6). Taken together, these data indicate that the process of CaOx internalization by renal tubular cells is similar to the endocytosis reported for other systems. These findings may be relevant to cellular phenomena involved in early stages of the formation of renal stones.Universidade Federal de São Paulo (UNIFESP)UNIFESPSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Campos, A.h. [UNIFESP]Schor, Nestor [UNIFESP]2015-06-14T13:24:58Z2015-06-14T13:24:58Z2000-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion111-118application/pdfhttp://dx.doi.org/10.1590/S0100-879X2000000100015Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 33, n. 1, p. 111-118, 2000.10.1590/S0100-879X2000000100015S0100-879X2000000100015.pdf0100-879XS0100-879X2000000100015http://repositorio.unifesp.br/handle/11600/882WOS:000085031800015engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T17:06:07Zoai:repositorio.unifesp.br/:11600/882Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T17:06:07Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
title |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
spellingShingle |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells Campos, A.h. [UNIFESP] calcium oxalate DCK cells mechanisms of endocytosis renal stone |
title_short |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
title_full |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
title_fullStr |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
title_full_unstemmed |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
title_sort |
Mechanisms involved in calcium oxalate endocytosis by Madin-Darby canine kidney cells |
author |
Campos, A.h. [UNIFESP] |
author_facet |
Campos, A.h. [UNIFESP] Schor, Nestor [UNIFESP] |
author_role |
author |
author2 |
Schor, Nestor [UNIFESP] |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Campos, A.h. [UNIFESP] Schor, Nestor [UNIFESP] |
dc.subject.por.fl_str_mv |
calcium oxalate DCK cells mechanisms of endocytosis renal stone |
topic |
calcium oxalate DCK cells mechanisms of endocytosis renal stone |
description |
Calcium oxalate (CaOx) crystals adhere to and are internalized by tubular renal cells and it seems that this interaction is related (positively or negatively) to the appearance of urinary calculi. The present study analyzes a series of mechanisms possibly involved in CaOx uptake by Madin-Darby canine kidney (MDCK) cells. CaOx crystals were added to MDCK cell cultures and endocytosis was evaluated by polarized light microscopy. This process was inhibited by an increase in intracellular calcium by means of ionomycin (100 nM; N = 6; 43.9% inhibition; P<0.001) or thapsigargin (1 µM; N = 6; 33.3% inhibition; P<0.005) administration, and via blockade of cytoskeleton assembly by the addition of colchicine (10 µM; N = 8; 46.1% inhibition; P<0.001) or cytochalasin B (10 µM; N = 8; 34.2% inhibition; P<0.001). Furthermore, CaOx uptake was reduced when the activity of protein kinase C was inhibited by staurosporine (10 nM; N = 6; 44% inhibition; P<0.01), or that of cyclo-oxygenase by indomethacin (3 µM; N = 12; 17.2% inhibition; P<0.05); however, the uptake was unaffected by modulation of potassium channel activity with glibenclamide (3 µM; N = 6), tetraethylammonium (1 mM; N = 6) or cromakalim (1 µM; N = 6). Taken together, these data indicate that the process of CaOx internalization by renal tubular cells is similar to the endocytosis reported for other systems. These findings may be relevant to cellular phenomena involved in early stages of the formation of renal stones. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-01-01 2015-06-14T13:24:58Z 2015-06-14T13:24:58Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0100-879X2000000100015 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 33, n. 1, p. 111-118, 2000. 10.1590/S0100-879X2000000100015 S0100-879X2000000100015.pdf 0100-879X S0100-879X2000000100015 http://repositorio.unifesp.br/handle/11600/882 WOS:000085031800015 |
url |
http://dx.doi.org/10.1590/S0100-879X2000000100015 http://repositorio.unifesp.br/handle/11600/882 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 33, n. 1, p. 111-118, 2000. 10.1590/S0100-879X2000000100015 S0100-879X2000000100015.pdf 0100-879X S0100-879X2000000100015 WOS:000085031800015 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
111-118 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268380401631232 |