ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2023 and some content may be unavailable. To unlock all content for 2023, please visit the archives.

Abstract: FR-PO323

Pharmacologic Pyruvate Kinase M2 Activation Maintains Mitochondrial Metabolism by Regulating the Interaction Between HIF-1α and PGC-1α in Diabetic Kidney Disease

Session Information

Category: Diabetic Kidney Disease

  • 701 Diabetic Kidney Disease: Basic

Authors

  • Kim, Gyu Ri, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Joo, Young Su, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Ryu, Jaejin, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Nam, Boyoung, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Park, Jung Tak, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Yoo, Tae-Hyun, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Kang, Shin-Wook, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
  • Han, Seung Hyeok, Yonsei University Institute of Kidney Disease, Seodaemun-gu, Seoul, Korea (the Republic of)
Background

Previous findings have indicated that pyruvate kinase isoform M2 (PKM2) activation may protect kidney injury by improving mitochondrial dysfunction and anerobic glycolysis. However, the underlying molecular mechanisms are incompletely understood. Here, we aimed to clarify mechanistic link between PKM2 and HIF-1α-mediated PGC-1α suppression in animal model of diabetic kidney disease (DKD).

Methods

In an animal DKD study, db/db mice were intraperitoneally injected with TEPP-46, a PKM2 activator. In vitro, primary cultured renal tubular epithelial cells (RTECs) from C57BL/6 mice were treated with high glucose (HG) alone and HG+TEPP-46. The interactions between HIF-1α and PGC1α were further investigated using HIF-1α overexpression and HIF-1α knockdown. PKM2 activity, energy metabolism, mitochondrial mass, dynamics, and morphology, and cell injury markers were examined.

Results

In the kidney of db/db mice, diabetes resulted in decreased PKM2 activation, aberrant glycolysis, impaired fatty acid oxidation, and decreased mitochondrial mass, integrity, and function. These changes were accompanied by increased HIF-1α and decreased PGC-1α levels. Increased fibrosis and apoptosis markers were observed in diabetic mice. In addition, periodic acid–Schiff (PAS) staining revealed significant tubular injury in db/db mice. The direct PKM2 activation by TEPP-46 treatment attenuated the dysregulated energy metabolism, mitochondrial dysfunction, and cell death. Similar alterations were also observed in HG-treated RTECs, which were restored by TEPP-46. Notably, a chromatin immunoprecipitation assay revealed that HIF-1α directly binds to the regulatory region of the Ppargc1a promoter and that this interaction is inversely dependent on PKM2 activation. A luciferase reporter assay showed that HIF-1α regulates the transcriptional activity of PGC-1α in a PKM2-dependent manner. Moreover, Hif1a overexpression suppressed PGC-1α and induced aberrant energy metabolism, mitochondrial dysfunction, and apoptosis. Conversely, these changes were reversed by HIF-1α knockdown.

Conclusion

PKM2 activation improves impaired mitochondrial metabolism and function by modulating HIF-1α and PGC-1α interactions in DKD.

Funding

  • Government Support – Non-U.S.