Cargando…
Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy
Ciliary neurotrophic factor (CNTF) is well known as a growth/survival factor of neuronal tissue. We investigated the expression of CNTF and its specific receptor alpha (CNTFRα) in a unilateral ureteral obstruction (UUO) model. Complete UUO was produced by left ureteral ligation in Sprague-Dawley rat...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Anatomists
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145847/ https://www.ncbi.nlm.nih.gov/pubmed/21829752 http://dx.doi.org/10.5115/acb.2011.44.2.85 |
_version_ | 1782209136233021440 |
---|---|
author | Lee, Byoung-Seung Choi, Jae-Youn Cha, Jung-Ho |
author_facet | Lee, Byoung-Seung Choi, Jae-Youn Cha, Jung-Ho |
author_sort | Lee, Byoung-Seung |
collection | PubMed |
description | Ciliary neurotrophic factor (CNTF) is well known as a growth/survival factor of neuronal tissue. We investigated the expression of CNTF and its specific receptor alpha (CNTFRα) in a unilateral ureteral obstruction (UUO) model. Complete UUO was produced by left ureteral ligation in Sprague-Dawley rats. The animals were sacrificed on days 1, 3, 5, 7, 14, 21, and 28 after UUO. The kidneys were fixed, and processed for both immunohistochemistry and in situ hybridization. CNTF immunoreactivity in sham-operated kidneys was observed only in the descending thin limb (DTL) of the loop of Henle. In UUO kidneys, CNTF expression was induced in the S3 segment (S3s) of the proximal tubule from day 1, and progressively expanded into the entire S3s and a part of the convoluted proximal tubules, distal tubules (DT), and glomerular parietal epithelium up to day 7. Upregulated CNTF expression was maintained to day 28. From day 14, the inner medullary collecting duct showed weak CNTF immunoreactivity. The CNTFRα mRNA hybridization signal in sham-operated kidneys was weakly detected in the DTL, DT, medullary thick ascending limb, and in a few S3s cells. After UUO, CNTFRα mRNA expression increased progressively in both the renal cortex and the medulla up to day 7 and increased expression was maintained until day 28. The results suggest that the S3s may be the principal induction site for CNTF in response to renal injury, and that CNTF may play a role in chronic renal injury. |
format | Online Article Text |
id | pubmed-3145847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Korean Association of Anatomists |
record_format | MEDLINE/PubMed |
spelling | pubmed-31458472011-08-09 Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy Lee, Byoung-Seung Choi, Jae-Youn Cha, Jung-Ho Anat Cell Biol Original Article Ciliary neurotrophic factor (CNTF) is well known as a growth/survival factor of neuronal tissue. We investigated the expression of CNTF and its specific receptor alpha (CNTFRα) in a unilateral ureteral obstruction (UUO) model. Complete UUO was produced by left ureteral ligation in Sprague-Dawley rats. The animals were sacrificed on days 1, 3, 5, 7, 14, 21, and 28 after UUO. The kidneys were fixed, and processed for both immunohistochemistry and in situ hybridization. CNTF immunoreactivity in sham-operated kidneys was observed only in the descending thin limb (DTL) of the loop of Henle. In UUO kidneys, CNTF expression was induced in the S3 segment (S3s) of the proximal tubule from day 1, and progressively expanded into the entire S3s and a part of the convoluted proximal tubules, distal tubules (DT), and glomerular parietal epithelium up to day 7. Upregulated CNTF expression was maintained to day 28. From day 14, the inner medullary collecting duct showed weak CNTF immunoreactivity. The CNTFRα mRNA hybridization signal in sham-operated kidneys was weakly detected in the DTL, DT, medullary thick ascending limb, and in a few S3s cells. After UUO, CNTFRα mRNA expression increased progressively in both the renal cortex and the medulla up to day 7 and increased expression was maintained until day 28. The results suggest that the S3s may be the principal induction site for CNTF in response to renal injury, and that CNTF may play a role in chronic renal injury. Korean Association of Anatomists 2011-06 2011-06-30 /pmc/articles/PMC3145847/ /pubmed/21829752 http://dx.doi.org/10.5115/acb.2011.44.2.85 Text en Copyright © 2011. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Byoung-Seung Choi, Jae-Youn Cha, Jung-Ho Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title | Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title_full | Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title_fullStr | Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title_full_unstemmed | Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title_short | Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
title_sort | expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145847/ https://www.ncbi.nlm.nih.gov/pubmed/21829752 http://dx.doi.org/10.5115/acb.2011.44.2.85 |
work_keys_str_mv | AT leebyoungseung expressionofciliaryneurotrophicfactoranditsreceptorinexperimentalobstructivenephropathy AT choijaeyoun expressionofciliaryneurotrophicfactoranditsreceptorinexperimentalobstructivenephropathy AT chajungho expressionofciliaryneurotrophicfactoranditsreceptorinexperimentalobstructivenephropathy |