Mitofusin 2 controls mitochondrial and synaptic dynamics of suprachiasmatic VIP neurons and related circadian rhythms

Loading...
Thumbnail Image

Identifiers

Publication date

Authors

Stoiljkovic, Milan
Son, Jae Eun
Hong, Hee-kyung
Eindle, Henko
Varela, Luis
Catarino, Jonathas
Gao, Xiao-Bing
Liu, Zong-Wu
Sotonyi, Peter
Diano, Sabrina

Advisors

Other responsabilities

Journal Title

Bibliographic citation

Stoiljkovic M, Song JE, Hong HK, Endle H, Varela L, Catarino J, Gao XB, Liu ZW, Sotonyi P, Diano S, Cedernaes J, Bass J, Horvath TL. Mitofusin 2 controls mitochondrial and synaptic dynamics of suprachiasmatic VIP neurons and related circadian rhythms. J Clin Invest. 2025 Jul 1;135(13):e185000.

Type of academic work

Academic degree

Abstract

[Abstract] Sustaining the strong rhythmic interactions between cellular adaptations and environmental cues has been posited as essential for preserving the physiological and behavioral alignment of an organism to the proper phase of the daily light/dark (LD) cycle. Here, we demonstrate that mitochondria and synaptic input organization of suprachiasmatic (SCN) vasoactive intestinal peptide–expressing (VIP-expressing) neurons showed circadian rhythmicity. Perturbed mitochondrial dynamics achieved by conditional ablation of the fusogenic protein mitofusin 2 (Mfn2) in VIP neurons caused disrupted circadian oscillation in mitochondria and synapses in SCN VIP neurons, leading to desynchronization of entrainment to the LD cycle in Mfn2-deficient mice that resulted in an advanced phase angle of their locomotor activity onset, alterations in core body temperature, and sleep-wake amount and architecture. Our data provide direct evidence of circadian SCN clock machinery dependence on high-performance, Mfn2-regulated mitochondrial dynamics in VIP neurons for maintaining the coherence in daily biological rhythms of the mammalian organism.

Description

Rights

Attribution 4.0 International
Attribution 4.0 International

Except where otherwise noted, this item's license is described as Attribution 4.0 International