Cargando…

BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation

BACKGROUND: BAMBI (BMP and Activin Membrane Bound Inhibitor) is considered to influence TGFβ and Wnt signaling, and thereby fibrosis. Surprisingly data on cell type-specific expression of BAMBI are not available. We therefore examined the localization, gene regulation, and protein turnover of BAMBI...

Descripción completa

Detalles Bibliográficos
Autores principales: Xavier, Sandhya, Gilbert, Victoria, Rastaldi, Maria Pia, Krick, Stefanie, Kollins, Dmitrij, Reddy, Anand, Bottinger, Erwin, Cohen, Clemens D., Schlondorff, Detlef
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945319/
https://www.ncbi.nlm.nih.gov/pubmed/20886049
http://dx.doi.org/10.1371/journal.pone.0012995
_version_ 1782187205859475456
author Xavier, Sandhya
Gilbert, Victoria
Rastaldi, Maria Pia
Krick, Stefanie
Kollins, Dmitrij
Reddy, Anand
Bottinger, Erwin
Cohen, Clemens D.
Schlondorff, Detlef
author_facet Xavier, Sandhya
Gilbert, Victoria
Rastaldi, Maria Pia
Krick, Stefanie
Kollins, Dmitrij
Reddy, Anand
Bottinger, Erwin
Cohen, Clemens D.
Schlondorff, Detlef
author_sort Xavier, Sandhya
collection PubMed
description BACKGROUND: BAMBI (BMP and Activin Membrane Bound Inhibitor) is considered to influence TGFβ and Wnt signaling, and thereby fibrosis. Surprisingly data on cell type-specific expression of BAMBI are not available. We therefore examined the localization, gene regulation, and protein turnover of BAMBI in kidneys. METHODOLOGY/PRINCIPAL FINDINGS: By immunofluorescence microscopy and by mRNA expression, BAMBI is restricted to endothelial cells of the glomerular and some peritubular capillaries and of arteries and veins in both murine and human kidneys. TGFβ upregulated mRNA of BAMBI in murine glomerular endothelial cells (mGEC). LPS did not downregulate mRNA for BAMBI in mGEC or in HUVECs. BAMBI mRNA had a half-life of only 60 minutes and was stabilized by cycloheximide, indicating post-transcriptional regulation due to AU-rich elements, which we identified in the 3′ untranslated sequence of both the human and murine BAMBI gene. BAMBI protein turnover was studied in HUVECs with BAMBI overexpression using a lentiviral system. Serum starvation as an inducer of autophagy caused marked BAMBI degradation, which could be totally prevented by inhibition of lysosomal and autolysosomal degradation with bafilomycin, and partially by inhibition of autophagy with 3-methyladenine, but not by proteasomal inhibitors. Rapamycin activates autophagy by inhibiting TOR, and resulted in BAMBI protein degradation. Both serum starvation and rapamycin increased the conversion of the autophagy marker LC3 from LC3-I to LC3-II and also enhanced co-staining for BAMBI and LC3 in autolysosomal vesicles. CONCLUSIONS/SIGNIFICANCE: 1. BAMBI localizes to endothelial cells in the kidney and to HUVECs. 2. BAMBI mRNA is regulated by post-transcriptional mechanisms. 3. BAMBI protein is regulated by lysosomal and autolysosomal degradation. The endothelial localization and the quick turnover of BAMBI may indicate novel, yet to be defined functions of this modulator for TGFβ and Wnt protein actions in the renal vascular endothelium in health and disease.
format Text
id pubmed-2945319
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29453192010-09-30 BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation Xavier, Sandhya Gilbert, Victoria Rastaldi, Maria Pia Krick, Stefanie Kollins, Dmitrij Reddy, Anand Bottinger, Erwin Cohen, Clemens D. Schlondorff, Detlef PLoS One Research Article BACKGROUND: BAMBI (BMP and Activin Membrane Bound Inhibitor) is considered to influence TGFβ and Wnt signaling, and thereby fibrosis. Surprisingly data on cell type-specific expression of BAMBI are not available. We therefore examined the localization, gene regulation, and protein turnover of BAMBI in kidneys. METHODOLOGY/PRINCIPAL FINDINGS: By immunofluorescence microscopy and by mRNA expression, BAMBI is restricted to endothelial cells of the glomerular and some peritubular capillaries and of arteries and veins in both murine and human kidneys. TGFβ upregulated mRNA of BAMBI in murine glomerular endothelial cells (mGEC). LPS did not downregulate mRNA for BAMBI in mGEC or in HUVECs. BAMBI mRNA had a half-life of only 60 minutes and was stabilized by cycloheximide, indicating post-transcriptional regulation due to AU-rich elements, which we identified in the 3′ untranslated sequence of both the human and murine BAMBI gene. BAMBI protein turnover was studied in HUVECs with BAMBI overexpression using a lentiviral system. Serum starvation as an inducer of autophagy caused marked BAMBI degradation, which could be totally prevented by inhibition of lysosomal and autolysosomal degradation with bafilomycin, and partially by inhibition of autophagy with 3-methyladenine, but not by proteasomal inhibitors. Rapamycin activates autophagy by inhibiting TOR, and resulted in BAMBI protein degradation. Both serum starvation and rapamycin increased the conversion of the autophagy marker LC3 from LC3-I to LC3-II and also enhanced co-staining for BAMBI and LC3 in autolysosomal vesicles. CONCLUSIONS/SIGNIFICANCE: 1. BAMBI localizes to endothelial cells in the kidney and to HUVECs. 2. BAMBI mRNA is regulated by post-transcriptional mechanisms. 3. BAMBI protein is regulated by lysosomal and autolysosomal degradation. The endothelial localization and the quick turnover of BAMBI may indicate novel, yet to be defined functions of this modulator for TGFβ and Wnt protein actions in the renal vascular endothelium in health and disease. Public Library of Science 2010-09-24 /pmc/articles/PMC2945319/ /pubmed/20886049 http://dx.doi.org/10.1371/journal.pone.0012995 Text en Xavier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xavier, Sandhya
Gilbert, Victoria
Rastaldi, Maria Pia
Krick, Stefanie
Kollins, Dmitrij
Reddy, Anand
Bottinger, Erwin
Cohen, Clemens D.
Schlondorff, Detlef
BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title_full BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title_fullStr BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title_full_unstemmed BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title_short BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation
title_sort bambi is expressed in endothelial cells and is regulated by lysosomal/autolysosomal degradation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945319/
https://www.ncbi.nlm.nih.gov/pubmed/20886049
http://dx.doi.org/10.1371/journal.pone.0012995
work_keys_str_mv AT xaviersandhya bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT gilbertvictoria bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT rastaldimariapia bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT krickstefanie bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT kollinsdmitrij bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT reddyanand bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT bottingererwin bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT cohenclemensd bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation
AT schlondorffdetlef bambiisexpressedinendothelialcellsandisregulatedbylysosomalautolysosomaldegradation