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

被引:51
作者
Xavier, Sandhya [1 ]
Gilbert, Victoria [1 ]
Rastaldi, Maria Pia [5 ]
Krick, Stefanie [1 ]
Kollins, Dmitrij [1 ]
Reddy, Anand [1 ]
Bottinger, Erwin [1 ]
Cohen, Clemens D. [2 ,3 ,4 ]
Schlondorff, Detlef [1 ]
机构
[1] Mt Sinai Sch Med, Dept Med, New York, NY USA
[2] Univ Hosp, Div Nephrol, Zurich, Switzerland
[3] Univ Hosp, Inst Physiol, Ctr Integrat Human Physiol, Zurich, Switzerland
[4] Univ Zurich, Zurich, Switzerland
[5] Fdn DAmico Ric Malattie Renali, Renal Immunopathol Lab, Milan, Italy
基金
美国国家卫生研究院; 瑞士国家科学基金会;
关键词
GROWTH-FACTOR-BETA; MEMBRANE-BOUND INHIBITOR; ISOLATED RAT HEPATOCYTES; TGF-BETA; GENE-EXPRESSION; PSEUDORECEPTOR BAMBI; PROTEIN-DEGRADATION; COLORECTAL-CANCER; MESANGIAL CELLS; AUTOPHAGY;
D O I
10.1371/journal.pone.0012995
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: BAMBI (BMP and Activin Membrane Bound Inhibitor) is considered to influence TGF beta 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. TGF beta 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 TGF beta and Wnt protein actions in the renal vascular endothelium in health and disease.
引用
收藏
页数:17
相关论文
共 56 条
[1]
Isolation, culture, and characterization of endothelial cells from mouse glomeruli [J].
Akis, N ;
Madaio, MP .
KIDNEY INTERNATIONAL, 2004, 65 (06) :2223-2227
[2]
AU-rich elements and associated factors: are there unifying principles? [J].
Barreau, C ;
Paillard, L ;
Osborne, HB .
NUCLEIC ACIDS RESEARCH, 2005, 33 (22) :7138-7150
[3]
Aquaporin expression in normal human kidney and in renal disease [J].
Bedford, JJ ;
Leader, JP ;
Walker, RJ .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (10) :2581-2587
[4]
The phosphatidylinositol 3-kinase inhibitors wortmannin and LY294002 inhibit autophagy in isolated rat hepatocytes [J].
Blommaart, EFC ;
Krause, U ;
Schellens, JPM ;
VreelingSindelarova, H ;
Meijer, AJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 243 (1-2) :240-246
[5]
TGF-β in renal injury and disease [J].
Bottinger, Erwin P. .
SEMINARS IN NEPHROLOGY, 2007, 27 (03) :309-320
[6]
The TGF-β pseudoreceptor gene Bambi is dispensable for mouse embryonic development and postnatal survival [J].
Chen, Jianquan ;
Bush, Jeffrey O. ;
Ovitt, Catherine E. ;
Lan, Yu ;
Jiang, Rulang .
GENESIS, 2007, 45 (08) :482-486
[7]
Quantitative gene expression analysis in renal biopsies:: A novel protocol for a high-throughput multicenter application [J].
Cohen, CD ;
Frach, K ;
Schlöndorff, D ;
Kretzler, M .
KIDNEY INTERNATIONAL, 2002, 61 (01) :133-140
[8]
High-level transduction and gene expression in hematopoietic repopulating cells using a human imunodeficiency virus type 1-based lentiviral vector containing an internal spleen focus forming virus promoter [J].
Demaison, C ;
Parsley, K ;
Brouns, G ;
Scherr, M ;
Battmer, K ;
Kinnon, C ;
Grez, M ;
Thrasher, AJ .
HUMAN GENE THERAPY, 2002, 13 (07) :803-813
[9]
PERMANENT CELL-LINE EXPRESSING HUMAN FACTOR-VIII-RELATED ANTIGEN ESTABLISHED BY HYBRIDIZATION [J].
EDGELL, CJ ;
MCDONALD, CC ;
GRAHAM, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (12) :3734-3737
[10]
Sepsis induces changes in the expression and distribution of Toll-like receptor 4 in the rat kidney [J].
El-Achkar, TM ;
Huang, XP ;
Plotkin, Z ;
Sandoval, RM ;
Rhodes, GJ ;
Dagher, PC .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (05) :F1034-F1043