# Cell-type specific effects of the long non-coding RNA HIF1A-AS3 on HIF1A expression in kidney cells

## TL;DR

This study explores how a specific long non-coding RNA, HIF1A-AS3, affects HIF1A expression in kidney cells under different conditions, revealing cell-type specific effects.

## Contribution

The paper identifies a cell-type specific regulatory role of HIF1A-AS3 on HIF1A expression in non-cancerous kidney cells.

## Key findings

- HIF1A-AS3 knockdown significantly reduces HIF1A-AS2 and Hif1α in HK-2 cells but not in mesangial cells.
- HIF1A-AS3 RNA is highly stable in HK-2 cells, as shown by Actinomycin D treatment.
- HIF1A-AS3 has a more pronounced effect on HIF1A expression than HIF1A-AS2.

## Abstract

The hypoxia-inducible factor 1α (Hif1α) represents the master transcription factor coordinating cellular responses to oxygen depletion. With hundreds of target genes it plays a key role in numerous bio-medical conditions as well as neoplastic and non-cancerous diseases, which in turn requires a strict regulation. Long non-coding RNAs have the potential to virtually control every step of gene expression. We aimed to investigate the expression and role of HIF1A antisense lncRNAs HIF1A-AS1, AS2, and AS3 under hyperglycemic, hypoxic, or both conditions in three non-cancerous human renal cell types: HK-2 cells, primary RPTECs, and mesangial cells. We observed that HIF1A-AS2 and AS3 expression was upregulated under oxygen deprivation. Furthermore, knockdown (KD) of HIF1A-AS3 resulted in a significant reduction of HIF1A-AS2 and even more important of Hif1α in HK-2 cells but not mesangial cells. While KD of HIF1A also had a diminishing effect on HIF1A-AS2 and AS3 RNA levels, KD of HIF1A-AS2 only affected HIF1A-AS3 but not HIF1A. Treating HK-2 cells with Actinomycin D revealed a high HIF1A-AS3 RNA stability. In conclusion, our data reveal a cell-type specific effect of HIF1A-AS3 on HIF1A RNA and protein expression which might allow the development of a cell-type specific HIF1A antagonist based on lncRNAs.

The online version contains supplementary material available at 10.1038/s41598-025-12441-5.