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Description
Growth and maintenance of skeletal muscle mass is critical for long-term health and quality of life. Muscle is
important for mobility but it is also crucial for metabolic health because of its contribution to glucose uptake
and fat metabolism. Our lab and others have demonstrated that signaling through the mammalian target of
rapamycin (mTOR) is necessary for skeletal muscle growth but the molecular links between signal input and
downstream function are far from understood. In our previous studies we showed that a) prolonged
activation of mTOR signaling is specific to growth inducing contractions, b) mechanical strain activates
mTOR signaling in skeletal muscle but not in non-muscle cells, c) strain-induced mTOR signaling is
independent of the IGF1/insulin/PI3 kinase signaling pathways, and d) cell cycle genes, such as cyclin D1
and c-myc, are induced during mTOR dependent growth and they likely function, in the differentiated muscle
cell, to induce ribosomal biogenesis/protein synthesis.
The overall goal of this research is to use in vitro and in vivo models of skeletal muscle growth with
molecular tools to identify the necessary upstream regulators and downstream effectors of mTOR. The two
main hypotheses are I) mechanical strain acts synergistically with growth factors to prolong activation of
mTOR signaling in skeletal muscle and II) mTOR dependent up-regulation of cyclin D and c-myc expression
is necessary for ribosomal biogenesis and increased protein synthesis. These hypotheses will be tested by
the following specific aims:
Specific Aim 1. To determine the molecular signals by which mechanical strain regulates mTOR signaling.
Specific Aim 2. To demonstrate whether mechanical signaling acts synergistically with IGF1 to regulate
growth-related mTOR function.
Specific Aim 3. To determine whether cyclin D or c-myc expression is necessary and/or sufficient for
ribosomal biogenesis and increased protein synthesis.
The results of these studies will provide novel insight for the field of mTOR regulation and the role of
mechanical strain in the growth process of skeletal muscle. The clinical implications of this work are also
significant and will contribute to development of strategies to attenuate or ameliorate muscle atrophy
associated with disuse, aging, bed rest and cachexia.
Status | Finished |
---|---|
Effective start/end date | 2/5/99 → 2/28/13 |
Funding
- National Institute Arthritis Musculoskeletal & Skin: $1,725,900.00
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Projects
- 1 Finished
-
Intracellular Signaling During Skeletal Muscle Hypertrophy - Research Supplement
Esser, K. & Park-Sarge, O.
National Institute Arthritis Musculoskeletal & Skin
2/5/99 → 2/28/12
Project: Research project