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Series GSE4316 Query DataSets for GSE4316
Status Public on Jun 21, 2006
Title Genome-wide expression profile of human trabecular meshwork cultured cells, non-glaucomatous and POAG tissue
Organism Homo sapiens
Experiment type Expression profiling by array
Summary The goal of this study was to contrast genome-wide gene expression profiles of cultured human trabecular meshwork (HTM) cells, to that of control and primary open angle glaucoma (POAG) HTM tissues.

Total RNA from cultured HTM cells and HTM tissue dissected from control and POAG anterior segments fixed in RNA laterâ„¢ was linearly amplified with the OvationTM Biotin RNA Amplification and Labeling System and individually hybridized to Affymetrix Human Genome U133 Plus 2.0 high density microarrays. Data analysis was performed using the GeneSpring Software 7.0. Selected genes showing significant differential expression were validated by Quantitative real-time PCR in nonamplified RNA.

Cultured HTM cells retained the expression of some genes characteristic of the HTM tissue, including chitinase 3-like 1 and matrix Gla protein, but demonstrated downregulation of physiologically important genes such as myocilin. POAG HTM tissue showed relatively small changes compared to that of control donors. These changes included the statistically significant upregulation of several genes associated with inflammation and acute-phase response, including selectin-E (ELAM-I), as well as the downregulation of the antioxidants, paraoxonase 3 and ceruloplasmin.

Downregulation in cultured HTM cells of genes potentially relevant for outflow pathway function highlights the importance of developing new conditions for the culture of TM cells capable of preserving the characteristics of TM cells in vivo. Comparative analysis between control and POAG tissues suggests that the upregulation of inflammation-associated genes might be involved in the progression of glaucoma.
Keywords: Cell type comparison
 
Overall design Total RNA from three cultured HTM cells and HTM tissue dissected from three pairs of control and two pairs of POAG anterior segments fixed in RNA laterâ„¢ was linearly amplified with the OvationTM Biotin RNA Amplification and Labeling System and individually hybridized to Affymetrix Human Genome U133 Plus 2.0 high density microarrays.
 
Contributor(s) Liton PB, Luna C, Challa P, Epstein DL, Gonzalez P
Citation(s) 16862071
Submission date Mar 01, 2006
Last update date Mar 25, 2019
Contact name Pedro Gonzalez
E-mail(s) gonza012@mc.duke.edu
Phone 9196815995
Fax 9196848983
Organization name Duke University
Department Ophthalmology
Lab Glaucoma
Street address Erwin Road Box 3802
City Durham
State/province NC
ZIP/Postal code 27710
Country USA
 
Platforms (1)
GPL570 [HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
Samples (8)
GSM98622 ControlTM-A
GSM98624 ControlTM-B
GSM98625 ControlTM-C
Relations
BioProject PRJNA94735

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Supplementary data files not provided

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