Molecular fingerprinting of the podocyte reveals novel gene and protein regulatory networks

被引:121
作者
Boerries, Melanie [1 ,2 ]
Grahammer, Florian [3 ]
Eiselein, Sven [1 ,2 ,4 ]
Buck, Moritz [1 ,2 ]
Meyer, Charlotte [3 ]
Goedel, Markus [3 ]
Bechtel, Wibke [3 ]
Zschiedrich, Stefan [3 ]
Pfeifer, Dietmar [5 ]
Laloe, Denis [6 ]
Arrondel, Christelle [7 ]
Goncalves, Sara [7 ]
Krueger, Marcus [8 ]
Harvey, Scott J. [7 ]
Busch, Hauke [1 ,2 ]
Dengjel, Joern [1 ,2 ,4 ]
Huber, Tobias B. [3 ,4 ]
机构
[1] Univ Freiburg, Freiburg Inst Adv Studies LifeNet, D-79106 Freiburg, Germany
[2] Univ Freiburg, Ctr Biol Syst Anal, D-79106 Freiburg, Germany
[3] Freiburg Univ Med Ctr, Div Renal, D-79106 Freiburg, Germany
[4] Univ Freiburg, BIOSS Ctr Biol Signalling Studies, D-79106 Freiburg, Germany
[5] Freiburg Univ Med Ctr, Dept Hematol & Oncol, D-79106 Freiburg, Germany
[6] INRA, UMR Genet Anim & Biol Integrat 1313, Jouy En Josas, France
[7] Hop Necker Enfants Malad, Inserm Avenir U983, Paris, France
[8] Max Planck Inst Heart & Lung Res, Bad Nauheim, Germany
关键词
gene expression; glomerulus; mass spectrometry; podocyte; proteomic analysis; QUANTITATIVE PROTEOMICS; NUCLEAR-ENVELOPE; EXPRESSION; KIDNEY; IDENTIFICATION; PREDICTION; ENRICHMENT; NEPH1;
D O I
10.1038/ki.2012.487
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A thorough characterization of the transcriptome and proteome of endogenous podocytes has been hampered by low cell yields during isolation. Here we describe a double fluorescent reporter mouse model combined with an optimized bead perfusion protocol and efficient single cell dissociation to yield more than 500,000 podocytes per mouse allowing for global, unbiased downstream applications. Combining mRNA and miRNA transcriptional profiling with quantitative proteomic analyses revealed programs of highly specific gene regulation tightly controlling cytoskeleton, cell differentiation, endosomal transport, and peroxisome function in podocytes. Strikingly, the analyses further predict that these podocyte-specific gene regulatory networks are accompanied by alternative splicing of respective genes. Thus, our 'omics' approach will facilitate the discovery and integration of novel gene, protein, and organelle regulatory networks that deepen our systematic understanding of podocyte biology.
引用
收藏
页码:1052 / 1064
页数:13
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