Research Paper Volume 8, Issue 9 pp 2062—2080

Age-associated repression of type 1 inositol 1, 4, 5-triphosphate receptor impairs muscle regeneration

Jeong Yi Choi1,2, , Chae Young Hwang1,3, , Bora Lee1,4, , Seung-Min Lee1, , Young Jae Bahn1, , Kwang-Pyo Lee1, , Moonkyung Kang5, , Yeon-Soo Kim5, , Sun-Hee Woo6, , Jae-Young Lim7, , Eunhee Kim2, , Ki-Sun Kwon1,4, ,

  • 1 Aging Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea
  • 2 College of Biological Science and Biotechnology, Chungnam National University, Daejeon 34134, Republic of Korea
  • 3 Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea
  • 4 Department of Functional Genomics, Korea University of Science and Technology, Daejeon 34113, Republic of Korea
  • 5 Graduate School of New Drug Discovery & Development, Chungnam National University, Daejeon 34143, Republic of Korea
  • 6 College of Pharmacy, Chungnam National University, Daejeon 34143, Republic of Korea
  • 7 Department of Rehabilitation Medicine, Seoul National University Bundang Hospital, Gyeonggi-do 13620, Republic of Korea
* Equal contribution

Received: June 6, 2016       Accepted: August 30, 2016       Published: September 21, 2016
How to Cite


Skeletal muscle mass and power decrease with age, leading to impairment of mobility and metabolism in the elderly. Ca2+ signaling is crucial for myoblast differentiation as well as muscle contraction through activation of transcription factors and Ca2+-dependent kinases and phosphatases. Ca2+ channels, such as dihydropyridine receptor (DHPR), two-pore channel (TPC) and inositol 1,4,5-triphosphate receptor (ITPR), function to maintain Ca2+ homeostasis in myoblasts. Here, we observed a significant decrease in expression of type 1 IP3 receptor (ITPR1), but not types 2 and 3, in aged mice skeletal muscle and isolated myoblasts, compared with those of young mice. ITPR1 knockdown using shRNA-expressing viruses in C2C12 myoblasts and tibialis anterior muscle of mice inhibited myotube formation and muscle regeneration after injury, respectively, a typical phenotype of aged muscle. This aging phenotype was associated with repression of muscle-specific genes and activation of the epidermal growth factor receptor (EGFR)-Ras-extracellular signal-regulated kinase (ERK) pathway. ERK inhibition by U0126 not only induced recovery of myotube formation in old myoblasts but also facilitated muscle regeneration after injury in aged muscle. The conserved decline in ITPR1 expression in aged human skeletal muscle suggests utility as a potential therapeutic target for sarcopenia, which can be treated using ERK inhibition strategies.


CTX: Cardiotoxin; DM: differentiation medium; GM: growth medium; ITPR1: inositol 1,4,5 triphosphate receptor type 1; MyHC: myosin heavy chain; TA: tibialis anterior.