AI Article Synopsis

  • Studies show kidney disease is linked to viral infections, causing kidney injury through systemic inflammation and direct infection of kidney cells.
  • Research using an immortalized human podocyte cell line (HPC) infected with lentivirus revealed strong immune responses and pathways related to cell death, indicating compromised cell viability.
  • The findings suggest that these lentivirus-infected HPC cells serve as a valuable model for studying how viral infections specifically damage podocytes, separate from other stressors like Adriamycin.

Article Abstract

A large number of studies have shown the association of kidney disease with viral infections in the body. Viral infections cause kidney injury in two manners, the systemic inflammation (cytokine storm) and the direct infection of kidney cells. Concerning direct viral infection of podocytes, the mechanism underlying virus-induced podocyte injury remains largely unknown and requires effective experimental models to facilitate its study. Here, we performed molecular characterization of immortalized human podocyte cell line (HPC) infected with lentivirus by RNA-seq. Bioinformatics analysis revealed a strong innate immune response in the cells, including interferon production and signaling. Meanwhile, activations of ferroptosis pathway and TNF-alpha signaling were also found, consistent with an impaired viability of the cells. Lentiviral infection also upregulated expression of APOL1 as observed in patients with HIV associated nephropathy (HIVAN) and diabetic nephropathy (DN). Interestingly, when the lentiviral infected cells were treated with Adriamycin (ADR), the ADR-associated signaling pathways were not interfered and remained activated as that in the cells treated with ADR only, suggesting that the virus and ADR have distinct mechanisms in damaging podocytes. Thus, the lentivirus-infected HPC cells represent a useful model of viral infection-associated podocytopathy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578807PMC
http://dx.doi.org/10.62347/BBCX1142DOI Listing

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