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Reorganization of mitochondria-organelle interactions during postnatal development in skeletal muscle.
Kim, Yuho; Parry, Hailey A; Willingham, T Bradley; Alspaugh, Greg; Lindberg, Eric; Combs, Christian A; Knutson, Jay R; Bleck, Christopher K E; Glancy, Brian.
Afiliação
  • Kim Y; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Parry HA; Department of Physical Therapy and Kinesiology, University of Massachusetts Lowell, Massachusetts, USA.
  • Willingham TB; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Alspaugh G; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Lindberg E; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Combs CA; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Knutson JR; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Bleck CKE; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Glancy B; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
J Physiol ; 602(5): 891-912, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38429930
ABSTRACT
Skeletal muscle cellular development requires the integrated assembly of mitochondria and other organelles adjacent to the sarcomere in support of muscle contractile performance. However, it remains unclear how interactions among organelles and with the sarcomere relates to the development of muscle cell function. Here, we combine 3D volume electron microscopy, proteomic analyses, and live cell functional imaging to investigate the postnatal reorganization of mitochondria-organelle interactions in skeletal muscle. We show that while mitochondrial networks are disorganized and loosely associated with the contractile apparatus at birth, contact sites among mitochondria, lipid droplets and the sarcoplasmic reticulum are highly abundant in neonatal muscles. The maturation process is characterized by a transition to highly organized mitochondrial networks wrapped tightly around the muscle sarcomere but also to less frequent interactions with both lipid droplets and the sarcoplasmic reticulum. Concomitantly, expression of proteins involved in mitochondria-organelle membrane contact sites decreases during postnatal development in tandem with a decrease in abundance of proteins associated with sarcomere assembly despite an overall increase in contractile protein abundance. Functionally, parallel measures of mitochondrial membrane potential, NADH redox status, and NADH flux within intact cells revealed that mitochondria in adult skeletal muscle fibres maintain a more activated electron transport chain compared with neonatal muscle mitochondria. These data demonstrate a developmental redesign reflecting a shift from muscle cell assembly and frequent inter-organelle communication toward a muscle fibre with mitochondrial structure, interactions, composition and function specialized to support contractile function. KEY POINTS Mitochondrial network organization is remodelled during skeletal muscle postnatal development. The mitochondrial outer membrane is in frequent contact with other organelles at birth and transitions to more close associations with the contractile apparatus in mature muscles. Mitochondrial energy metabolism becomes more activated during postnatal development. Understanding the developmental redesign process within skeletal muscle cells may help pinpoint specific areas of deficit in muscles with developmental disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / NAD Limite: Adult / Humans / Newborn Idioma: En Revista: J Physiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / NAD Limite: Adult / Humans / Newborn Idioma: En Revista: J Physiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido