Description
Purpose: we performed comparative RNA-seq analyses to identify molecular network characteristics of kidney injury at different ischemia times; Methods: Unilateral clamping of the left renal pedicle plus contralateral nephrectomy was performed. Briefly, mice were anesthetized, right kidney was excised. The left kidney was clamped for indicated minutes (0min for sham-24h group, 16min for uIRIx16min-24h group, 18minfor uIRIx18min-24h group, 20min for uIRIx20min-24h group, 22min for uIRIx22min-24h group, 24min for uIRIx24min-24h group, 26min for uIRIx26min-24h group, 28min for uIRIx28min-24h group, 30min for uIRIx30min-24h group). Mice were placed on 37C heating platform while operation, ischemia and before awakening. At 24h after ischemia, mice were anesthetized and blood was taken to detect creatinine, kidney was harvest for PAS staining and mRNA seq.; Results: After sequence, the clean reads rate of all samples were 98%.The quality of the assembled transcriptome is good enough for functional annotation and further analysis.; Conclusions: We performed RNA-sequencing (RNA-Seq) analyses to identify molecular network characteristics of kidney injury at different ischemia time.
Overall Design
We performed RNA-sequencing (RNA-Seq) on kidney of 9 groups.; ; Grant No. : 82100713; Grant title:The role and mechanism of PFKFB3 in promoting fibrosis after acute kidney injury by regulating the metabolic reprogramming of renal tubular epithelial cells.; Name of the funding source: the National Natural Science Foundation of China.
Curator
yq_pan