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CorrigendumCardiology Free access | 10.1172/JCI23073C1

PI3K rescues the detrimental effects of chronic Akt activation in the heart during ischemia/reperfusion injury

Tomohisa Nagoshi, Takashi Matsui, Takuma Aoyama, Annarosa Leri, Piero Anversa, Ling Li, Wataru Ogawa, Federica del Monte, Judith K. Gwathmey, Luanda Grazette, Brian Hemmings, David A. Kass, Hunter C. Champion, and Anthony Rosenzweig

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Published February 1, 2006 - More info

Published in Volume 116, Issue 2 on February 1, 2006
J Clin Invest. 2006;116(2):548–548. https://doi.org/10.1172/JCI23073C1.
© 2006 The American Society for Clinical Investigation
Published February 1, 2006 - Version history
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PI3K rescues the detrimental effects of chronic Akt activation in the heart during ischemia/reperfusion injury
Tomohisa Nagoshi, … , Hunter C. Champion, Anthony Rosenzweig
Tomohisa Nagoshi, … , Hunter C. Champion, Anthony Rosenzweig
Research Article Cardiology

PI3K rescues the detrimental effects of chronic Akt activation in the heart during ischemia/reperfusion injury

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Abstract

Acute activation of the serine-threonine kinase Akt is cardioprotective and reduces both infarction and dysfunction after ischemia/reperfusion injury (IRI). However, less is known about the chronic effects of Akt activation in the heart, and, paradoxically, Akt is activated in samples from patients with chronic heart failure. We generated Tg mice with cardiac-specific expression of either activated (myristoylated [myr]) or dominant-negative (dn) Akt and assessed their response to IRI in an ex vivo model. While dn-Akt hearts demonstrated a moderate reduction in functional recovery after IRI, no function was restored in any of the myr-Akt–Tg hearts. Moreover, infarcts were dramatically larger in myr-Akt–Tg hearts. Biochemical analyses demonstrated that chronic Akt activation induces feedback inhibition of PI3K activity through both proteasome-dependent degradation of insulin receptor substrate–1 (IRS-1) and inhibition of transcription of IRS-1 as well as that of IRS-2. To test the functional significance of these signaling changes, we performed in vivo cardiac gene transfer with constitutively active PI3K in myr-Akt–Tg mice. Restoration of PI3K rescued function and reduced injury after IRI. These data demonstrate that PI3K-dependent but Akt-independent effectors are required for full cardioprotection and suggest a mechanism by which chronic Akt activation can become maladaptive.

Authors

Tomohisa Nagoshi, Takashi Matsui, Takuma Aoyama, Annarosa Leri, Piero Anversa, Ling Li, Wataru Ogawa, Federica del Monte, Judith K. Gwathmey, Luanda Grazette, Brian Hemmings, David A. Kass, Hunter C. Champion, Anthony Rosenzweig

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Original citation: J Clin Invest. 2005;115(8):2128–2138. doi:10.1172/JCI23073.

Citation for this corrigendum: J Clin Invest. 2006;116(2):548. doi:10.1172/JCI23073C1.

In the original author list, Brian A. Hemmings’s name appeared incorrectly. The corrected author list appears above.

The authors regret this error.

Version history
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