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Series GSE69123 Query DataSets for GSE69123
Status Public on Jan 30, 2023
Title Genome-wide transcriptional alterations during vascular growth in skeletal muscles of type 2 diabetic mice in response to femoral artery ligation
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Diabetes is a major risk factor of cardiovascular disease including coronary and peripheral arterial disease, attributed to impaired arteriogenesis and angiogenesis. Mechanisms behind them are poorly understood due to the complexity of these processes in presence of diabetes. To understand the cellular and molecular mechanisms underlying impaired adaptive vascular responses in type 2 diabetic (T2DM) mouse models of hindlimb ischemia using Genome-wide mRNA sequencing.In response to FAL, collateral density and lumen area were significantly reduced in adductor muscles of T2DM mice at day 7 and 14 days post-FAL. mRNA sequencing suggested an altered gene expression typical for monocyte and macrophage (Mϕ) subsets. Similarly, gene expressions typical of dendritic cell and lymphocyte were altered in adductor muscles of T2DM mice. Ischemic muscles of T2DM mice displayed impaired angiogenesis as revealed by endothelial staining. mRNA sequencing suggested downregulation of crucial genes implicated in angiogenesis and differential expression of genes typical for Mϕ subsets. Immunohistochemistry analysis corroborated with the mRNA sequencing analysis, suggesting an altered Mϕ polarization behind the impaired arteriogenesis and angiogenesis seen in T2DM mouse models of hindlimb ischemia.
 
Overall design Hindlimb ischemia was induced by femoral artery ligation (FAL). Arteriole and capillary parameters together with blood flow were analyzed from normoxic adductor and ischemic gastrocnemius muscles respectively, at day 7 and 14 post-FAL. Total RNA was isolated from both adductor and gastrocnemius muscles at day 7 post-FAL and sequencing was performed with libraries prepared from Poly (A) RNA fraction, using Illumina Genome Analyzer II.
 
Contributor(s) Mohan B, Kaikkonen MU, Ylä-Herttuala S
Citation(s) 36384268
Submission date May 21, 2015
Last update date Jan 31, 2023
Contact name Minna U Kaikkonen
E-mail(s) minna.kaikkonen@uef.fi
Organization name University of Eastern Finland
Department A.I. Virtanen Institute, Department of Biotechnology and Molecular Medicine
Street address P.O. Box 1627
City Kuopio
ZIP/Postal code 70211
Country Finland
 
Platforms (1)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
Samples (24)
GSM1693140 Control_Adductor_1
GSM1693141 Control_Adductor_2
GSM1693142 Control_Adductor_3
Relations
BioProject PRJNA284606
SRA SRP058586

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE69123_GeneExpression_RPKM.txt.gz 7.3 Mb (ftp)(http) TXT
GSE69123_RAW.tar 1.0 Gb (http)(custom) TAR (of BEDGRAPH)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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