ATP synthase inhibitory factor 1 (IF1), a novel myokine, regulates glucose metabolism by AMPK and Akt dual pathways. Issue 12 (31st October 2019)
- Record Type:
- Journal Article
- Title:
- ATP synthase inhibitory factor 1 (IF1), a novel myokine, regulates glucose metabolism by AMPK and Akt dual pathways. Issue 12 (31st October 2019)
- Main Title:
- ATP synthase inhibitory factor 1 (IF1), a novel myokine, regulates glucose metabolism by AMPK and Akt dual pathways
- Authors:
- Lee, Hye Jeong
Moon, Jiyoung
Chung, InHyeok
Chung, Ji Hyung
Park, Chan
Lee, Jung Ok
Han, Jeong Ah
Kang, Min Ju
Yoo, Eun Hye
Kwak, So‐Young
Jo, Garam
Park, Wonil
Park, Jonghoon
Kim, Kyoung Min
Lim, Soo
Ngoei, Kevin R. W.
Ling, Naomi X. Y.
Oakhill, Jonathan S.
Galic, Sandra
Murray‐Segal, Lisa
Kemp, Bruce E.
Mantzoros, Christos S.
Krauss, Ronald M.
Shin, Min‐Jeong
Kim, Hyeon Soo - Abstract:
- Abstract : ATPase inhibitory factor 1 (IF1) is an ATP synthase‐interacting protein that suppresses the hydrolysis activity of ATP synthase. In this study, we observed that the expression of IF1 was up‐regulated in response to electrical pulse stimulation of skeletal muscle cells and in exercized mice and healthy men. IF1 stimulates glucose uptake via AMPK in skeletal muscle cells and primary cultured myoblasts. Reactive oxygen species and Rac family small GTPase 1 (Rac1) function in the upstream and downstream of AMPK, respectively, in IF1‐mediated glucose uptake. In diabetic animal models, the administration of recombinant IF1 improved glucose tolerance and down‐regulated blood glucose level. In addition, IF1 inhibits ATP hydrolysis by β‐F1‐ATPase in plasma membrane, thereby increasing extracellular ATP and activating the protein kinase B (Akt) pathway, ultimately leading to glucose uptake. Thus, we suggest that IF1 is a novel myokine and propose a mechanism by which AMPK and Akt contribute independently to IF1‐mediated improvement of glucose tolerance impairment. These results demonstrate the importance of IF1 as a potential antidiabetic agent.—Lee, H. J., Moon, J., Chung, I., Chung, J. H., Park, C., Lee, J. O., Han, J. A., Kang, M. J., Yoo, E. H., Kwak, S.‐Y., Jo, G., Park, W., Park, J., Kim, K. M., Lim, S., Ngoei, K. R. W., Ling, N. X. Y., Oakhill, J. S., Galic, S., Murray‐Segal, L., Kemp, B. E., Mantzoros, C. S., Krauss, R. M., Shin, M.‐J., Kim, H. S. ATP synthaseAbstract : ATPase inhibitory factor 1 (IF1) is an ATP synthase‐interacting protein that suppresses the hydrolysis activity of ATP synthase. In this study, we observed that the expression of IF1 was up‐regulated in response to electrical pulse stimulation of skeletal muscle cells and in exercized mice and healthy men. IF1 stimulates glucose uptake via AMPK in skeletal muscle cells and primary cultured myoblasts. Reactive oxygen species and Rac family small GTPase 1 (Rac1) function in the upstream and downstream of AMPK, respectively, in IF1‐mediated glucose uptake. In diabetic animal models, the administration of recombinant IF1 improved glucose tolerance and down‐regulated blood glucose level. In addition, IF1 inhibits ATP hydrolysis by β‐F1‐ATPase in plasma membrane, thereby increasing extracellular ATP and activating the protein kinase B (Akt) pathway, ultimately leading to glucose uptake. Thus, we suggest that IF1 is a novel myokine and propose a mechanism by which AMPK and Akt contribute independently to IF1‐mediated improvement of glucose tolerance impairment. These results demonstrate the importance of IF1 as a potential antidiabetic agent.—Lee, H. J., Moon, J., Chung, I., Chung, J. H., Park, C., Lee, J. O., Han, J. A., Kang, M. J., Yoo, E. H., Kwak, S.‐Y., Jo, G., Park, W., Park, J., Kim, K. M., Lim, S., Ngoei, K. R. W., Ling, N. X. Y., Oakhill, J. S., Galic, S., Murray‐Segal, L., Kemp, B. E., Mantzoros, C. S., Krauss, R. M., Shin, M.‐J., Kim, H. S. ATP synthase inhibitory factor 1 (IF1), a novel myokine, regulates glucose metabolism by AMPK and Akt dual pathways. FASEB J. 33, 14825‐14840 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 12(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 12(2019)
- Issue Display:
- Volume 33, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 12
- Issue Sort Value:
- 2019-0033-0012-0000
- Page Start:
- 14825
- Page End:
- 14840
- Publication Date:
- 2019-10-31
- Subjects:
- diabetes -- glucose uptake
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201901440RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15336.xml