[HTML][HTML] End-stage renal disease is different from chronic kidney disease in upregulating ROS-modulated proinflammatory secretome in PBMCs-A novel multiple-hit …
Redox biology, 2020•Elsevier
Background The molecular mechanisms underlying chronic kidney disease (CKD) transition
to end-stage renal disease (ESRD) and CKD acceleration of cardiovascular and other tissue
inflammations remain poorly determined. Methods We conducted a comprehensive data
analyses on 7 microarray datasets in peripheral blood mononuclear cells (PBMCs) from
patients with CKD and ESRD from NCBI-GEO databases, where we examined the
expressions of 2641 secretome genes (SG). Results 1) 86.7% middle class (molecular …
to end-stage renal disease (ESRD) and CKD acceleration of cardiovascular and other tissue
inflammations remain poorly determined. Methods We conducted a comprehensive data
analyses on 7 microarray datasets in peripheral blood mononuclear cells (PBMCs) from
patients with CKD and ESRD from NCBI-GEO databases, where we examined the
expressions of 2641 secretome genes (SG). Results 1) 86.7% middle class (molecular …
Background
The molecular mechanisms underlying chronic kidney disease (CKD) transition to end-stage renal disease (ESRD) and CKD acceleration of cardiovascular and other tissue inflammations remain poorly determined.
Methods
We conducted a comprehensive data analyses on 7 microarray datasets in peripheral blood mononuclear cells (PBMCs) from patients with CKD and ESRD from NCBI-GEO databases, where we examined the expressions of 2641 secretome genes (SG).
Results
1) 86.7% middle class (molecular weight >500 Daltons) uremic toxins (UTs) were encoded by SGs; 2) Upregulation of SGs in PBMCs in patients with ESRD (121 SGs) were significantly higher than that of CKD (44 SGs); 3) Transcriptomic analyses of PBMC secretome had advantages to identify more comprehensive secretome than conventional secretomic analyses; 4) ESRD-induced SGs had strong proinflammatory pathways; 5) Proinflammatory cytokines-based UTs such as IL-1β and IL-18 promoted ESRD modulation of SGs; 6) ESRD-upregulated co-stimulation receptors CD48 and CD58 increased secretomic upregulation in the PBMCs, which were magnified enormously in tissues; 7) M1-, and M2-macrophage polarization signals contributed to ESRD- and CKD-upregulated SGs; 8) ESRD- and CKD-upregulated SGs contained senescence-promoting regulators by upregulating proinflammatory IGFBP7 and downregulating anti-inflammatory TGF-β1 and telomere stabilizer SERPINE1/PAI-1; 9) ROS pathways played bigger roles in mediating ESRD-upregulated SGs (11.6%) than that in CKD-upregulated SGs (6.8%), and half of ESRD-upregulated SGs were ROS-independent.
Conclusions
Our analysis suggests novel secretomic upregulation in PBMCs of patients with CKD and ESRD, act synergistically with uremic toxins, to promote inflammation and potential disease progression. Our findings have provided novel insights on PBMC secretome upregulation to promote disease progression and may lead to the identification of new therapeutic targets for novel regimens for CKD, ESRD and their accelerated cardiovascular disease, other inflammations and cancers. (Total words: 279).
Elsevier
