BioGPS
  • Home
  • Help
  • Plugins
  • Datasets
  • Sign Up
  • Login
Examples: Gene Symbol(s), Gene Ontology, Splicing plugins, Melanoma datasets
advanced
Home › Dataset Library › Expression data from human with IgA nephropathy (IgAN) [HG-U133A]

Dataset: Expression data from human with IgA nephropathy (IgAN) [HG-U133A]

Proteinuria is the most important predictor of outcome in glomerulonephritis and experimental data suggest that the tubular cell response...

Registered by ArrayExpress Uploader
View Dataset

Proteinuria is the most important predictor of outcome in glomerulonephritis and experimental data suggest that the tubular cell response to proteinuria is an important determinant of progressive fibrosis in the kidney. However, it is unclear whether proteinuria is a marker of disease severity or has a direct effect on tubular cells in the kidneys of patients with glomerulonephritis. Accordingly we studied an in vitro model of proteinuria, and identified 231 albumin-regulated genes differentially expressed by primary human kidney tubular epithelial cells exposed to albumin. We translated these findings to human disease by studying mRNA levels of these genes in the tubulo-interstitial compartment of kidney biopsies from patients with IgA nephropathy using microarrays. Biopsies from patients with IgAN (n=25) could be distinguished from those of control subjects (n=6) based solely upon the expression of these 231 albumin-regulated genes. The expression of an 11-transcript subset related to the degree of proteinuria, and this 11-mRNA subset was also sufficient to distinguish biopsies of subjects with IgAN from control biopsies. We tested if these findings could be extrapolated to other proteinuric diseases beyond IgAN and found that the all forms of primary glomerulonephritis (n=33) can be distinguished from controls (n=21) based solely on the expression levels of these 11 genes derived from our in vitro proteinuria model. Pathway analysis suggests common regulatory elements shared by these 11 transcripts. In conclusion, we have identified an albumin-regulated 11-gene signature shared between all forms of primary glomerulonephritis. Our findings support the hypothesis that albuminuria may directly promote injury in the tubulo-interstitial compartment of the kidney in patients with glomerulonephritis. We used microarrays to analyze the transcriptome of microdissected renal biopsies from patients with IgA nephropathy (IgAN) RNA from tubulointerstitial compartments was extracted and processed for hybridization on Affymetrix HG-U133A microarrays.

Species:
human

Samples:
31

Source:
E-GEOD-35487

Updated:
Dec.12, 2014

Registered:
Jun.18, 2014


Factors: (via ArrayExpress)
Sample
GSM869344 1
GSM869343 1
GSM869342 1
GSM869341 1
GSM869340 1
GSM869339 1
GSM869338 1
GSM869337 1
GSM869336 1
GSM869335 1
GSM869334 1
GSM869333 1
GSM869332 1
GSM869331 1
GSM869330 1
GSM869329 1
GSM869328 1
GSM869327 1
GSM869326 1
GSM869325 1
GSM869324 1
GSM869323 1
GSM869322 1
GSM869321 1
GSM869320 1
GSM869319 1
GSM869318 1
GSM869317 1
GSM869316 1
GSM869315 1
GSM869311 1

Tags

  • cell
  • compartment
  • disease
  • glomerulonephritis
  • iga nephropathy
  • kidney
  • proteinuria

Other Formats

JSON    XML
  • About
  • Blog
  • Help
  • FAQ
  • Downloads
  • API
  • iPhone App
  • Email updates
© 2025 The Scripps Research Institute. All rights reserved. (ver 94eefe6 )
  • Terms of Use