Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of rat embryonic kidney timepoints and a budded WD-MM recombination tissue


ABSTRACT: Here we compared the expression of an engineered kidney tissue, created by recombining an in vitro budded Wolffian duct with fresh E13 metanephric mesenchyme, with that of three in vivo rat embryonic kidney timepoints (E13, E18, and week 4) Experiment Overall Design: The global gene expression of recombined tissue (non-branched in vitro-formed UBs and MM) was analyzed and compared to the gene expression of early, late, and post developmental kidneys in order to determine whether normal developmental pathways were being followed. Genes with at least a 3-fold difference in expression between any of the 4 conditions (E13, E18, Wk4, recombined tissue) were analyzed and grouped into one of ten expression patterns. The expression of each group of genes was analyzed in the recombined tissue to compare the recombined tissue gene expression levels to the three in vivo time points.

ORGANISM(S): Rattus norvegicus

SUBMITTER: Sanjay Nigam 

PROVIDER: E-GEOD-9570 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Staged in vitro reconstitution and implantation of engineered rat kidney tissue.

Rosines E E   Sampogna R V RV   Johkura K K   Vaughn D A DA   Choi Y Y   Sakurai H H   Shah M M MM   Nigam S K SK  

Proceedings of the National Academy of Sciences of the United States of America 20071217 52


A major hurdle for current xenogenic-based and other approaches aimed at engineering kidney tissues is reproducing the complex three-dimensional structure of the kidney. Here, a stepwise, in vitro method of engineering rat kidney-like tissue capable of being implanted is described. Based on the fact that the stages of kidney development are separable into in vitro modules, an approach was devised that sequentially induces an epithelial tubule (the Wolffian duct) to undergo in vitro budding, foll  ...[more]

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