author_facet Crisman, Jacqueline M.
Richards, Laura L.
Valach, Daniel P.
Franzoni, David F.
Diamond, Jonathan R.
Crisman, Jacqueline M.
Richards, Laura L.
Valach, Daniel P.
Franzoni, David F.
Diamond, Jonathan R.
author Crisman, Jacqueline M.
Richards, Laura L.
Valach, Daniel P.
Franzoni, David F.
Diamond, Jonathan R.
spellingShingle Crisman, Jacqueline M.
Richards, Laura L.
Valach, Daniel P.
Franzoni, David F.
Diamond, Jonathan R.
Nephron Experimental Nephrology
Chemokine Expression in the Obstructed Kidney
Nephrology
Genetics
Physiology
General Medicine
author_sort crisman, jacqueline m.
spelling Crisman, Jacqueline M. Richards, Laura L. Valach, Daniel P. Franzoni, David F. Diamond, Jonathan R. 1660-2129 S. Karger AG Nephrology Genetics Physiology General Medicine http://dx.doi.org/10.1159/000052618 <jats:p>Chemokines are chemotactic cytokines that are important mediators of leukocyte extravasation and chemotaxis. Herein, we provide evidence that after 1 day of unilateral ureteral obstruction (UUO), the mouse obstructed kidney (OBK) expresses MCP-1 (monocyte chemoattractant protein-1), RANTES (Regulated on activation normal T-cell expressed and secreted) and IP-10 (interferon-γ-induced protein-10). In addition, by day 7, MIP-2 (macrophage inflammatory protein-2) expression is elevated in the obstructed kidneys compared to the contralateral control kidneys (CLK). After 7 days of obstruction, RANTES was the most abundant of the four chemokines detected in the OBK. In situ hybridization results indicate that several cellular compartments contribute to the expression of RANTES in the OBK. However, clearly cortical tubules within the OBK contribute substantially to the elevated expression of RANTES. These data support the contention that the cortical tubular epithelium plays a pivotal role in the inflammation associated with experimental hydronephrosis.</jats:p> Chemokine Expression in the Obstructed Kidney Nephron Experimental Nephrology
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series Nephron Experimental Nephrology
source_id 49
title Chemokine Expression in the Obstructed Kidney
title_unstemmed Chemokine Expression in the Obstructed Kidney
title_full Chemokine Expression in the Obstructed Kidney
title_fullStr Chemokine Expression in the Obstructed Kidney
title_full_unstemmed Chemokine Expression in the Obstructed Kidney
title_short Chemokine Expression in the Obstructed Kidney
title_sort chemokine expression in the obstructed kidney
topic Nephrology
Genetics
Physiology
General Medicine
url http://dx.doi.org/10.1159/000052618
publishDate 2001
physical 241-248
description <jats:p>Chemokines are chemotactic cytokines that are important mediators of leukocyte extravasation and chemotaxis. Herein, we provide evidence that after 1 day of unilateral ureteral obstruction (UUO), the mouse obstructed kidney (OBK) expresses MCP-1 (monocyte chemoattractant protein-1), RANTES (Regulated on activation normal T-cell expressed and secreted) and IP-10 (interferon-γ-induced protein-10). In addition, by day 7, MIP-2 (macrophage inflammatory protein-2) expression is elevated in the obstructed kidneys compared to the contralateral control kidneys (CLK). After 7 days of obstruction, RANTES was the most abundant of the four chemokines detected in the OBK. In situ hybridization results indicate that several cellular compartments contribute to the expression of RANTES in the OBK. However, clearly cortical tubules within the OBK contribute substantially to the elevated expression of RANTES. These data support the contention that the cortical tubular epithelium plays a pivotal role in the inflammation associated with experimental hydronephrosis.</jats:p>
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author Crisman, Jacqueline M., Richards, Laura L., Valach, Daniel P., Franzoni, David F., Diamond, Jonathan R.
author_facet Crisman, Jacqueline M., Richards, Laura L., Valach, Daniel P., Franzoni, David F., Diamond, Jonathan R., Crisman, Jacqueline M., Richards, Laura L., Valach, Daniel P., Franzoni, David F., Diamond, Jonathan R.
author_sort crisman, jacqueline m.
container_issue 4
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container_title Nephron Experimental Nephrology
container_volume 9
description <jats:p>Chemokines are chemotactic cytokines that are important mediators of leukocyte extravasation and chemotaxis. Herein, we provide evidence that after 1 day of unilateral ureteral obstruction (UUO), the mouse obstructed kidney (OBK) expresses MCP-1 (monocyte chemoattractant protein-1), RANTES (Regulated on activation normal T-cell expressed and secreted) and IP-10 (interferon-γ-induced protein-10). In addition, by day 7, MIP-2 (macrophage inflammatory protein-2) expression is elevated in the obstructed kidneys compared to the contralateral control kidneys (CLK). After 7 days of obstruction, RANTES was the most abundant of the four chemokines detected in the OBK. In situ hybridization results indicate that several cellular compartments contribute to the expression of RANTES in the OBK. However, clearly cortical tubules within the OBK contribute substantially to the elevated expression of RANTES. These data support the contention that the cortical tubular epithelium plays a pivotal role in the inflammation associated with experimental hydronephrosis.</jats:p>
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institution DE-Gla1, DE-Zi4, DE-15, DE-Rs1, DE-Pl11, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161
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spelling Crisman, Jacqueline M. Richards, Laura L. Valach, Daniel P. Franzoni, David F. Diamond, Jonathan R. 1660-2129 S. Karger AG Nephrology Genetics Physiology General Medicine http://dx.doi.org/10.1159/000052618 <jats:p>Chemokines are chemotactic cytokines that are important mediators of leukocyte extravasation and chemotaxis. Herein, we provide evidence that after 1 day of unilateral ureteral obstruction (UUO), the mouse obstructed kidney (OBK) expresses MCP-1 (monocyte chemoattractant protein-1), RANTES (Regulated on activation normal T-cell expressed and secreted) and IP-10 (interferon-γ-induced protein-10). In addition, by day 7, MIP-2 (macrophage inflammatory protein-2) expression is elevated in the obstructed kidneys compared to the contralateral control kidneys (CLK). After 7 days of obstruction, RANTES was the most abundant of the four chemokines detected in the OBK. In situ hybridization results indicate that several cellular compartments contribute to the expression of RANTES in the OBK. However, clearly cortical tubules within the OBK contribute substantially to the elevated expression of RANTES. These data support the contention that the cortical tubular epithelium plays a pivotal role in the inflammation associated with experimental hydronephrosis.</jats:p> Chemokine Expression in the Obstructed Kidney Nephron Experimental Nephrology
spellingShingle Crisman, Jacqueline M., Richards, Laura L., Valach, Daniel P., Franzoni, David F., Diamond, Jonathan R., Nephron Experimental Nephrology, Chemokine Expression in the Obstructed Kidney, Nephrology, Genetics, Physiology, General Medicine
title Chemokine Expression in the Obstructed Kidney
title_full Chemokine Expression in the Obstructed Kidney
title_fullStr Chemokine Expression in the Obstructed Kidney
title_full_unstemmed Chemokine Expression in the Obstructed Kidney
title_short Chemokine Expression in the Obstructed Kidney
title_sort chemokine expression in the obstructed kidney
title_unstemmed Chemokine Expression in the Obstructed Kidney
topic Nephrology, Genetics, Physiology, General Medicine
url http://dx.doi.org/10.1159/000052618