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Cellular hypertrophy

Cellular hypertrophy. Control of protein synthesis Endogenous Nutrient status Functional adequacy History Exogenous Nutrient availability Growth factors Space General phenomenon, muscle context. Immediate controls on protein synthesis. Substrate availability m-/t-RNA Amino acids

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Cellular hypertrophy

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  1. Cellular hypertrophy • Control of protein synthesis • Endogenous • Nutrient status • Functional adequacy • History • Exogenous • Nutrient availability • Growth factors • Space • General phenomenon, muscle context

  2. Immediate controls on protein synthesis • Substrate availability • m-/t-RNA • Amino acids • Catalyst availability & activity • rRNA & S6 phosphorylation • eIF2, 4 • eEF1, 2

  3. Stimuli for muscle size change • Developmental • Strongly dependent on growth factors • Feedforward • Mechanical • Overload (high force, short time) • Overwork (low force, long time) • Endogenous factors • Feedback • Integrative • Autocrine/paracrine factors

  4. Linking growth stimuli to growth • Insulin/IGF-1 • IGF1IGF1RIRS1 Grb2SOSRasRafMEKERKMNK--|4EBP1 PI3K • PI3K • IGF1/FAKPI3KPIP3PDK1akt --|TSC--|RhebmTOR RSKS6translational apparatus --|4EBP--|eIF4Etranslational activity --|eEF2K--|eEF2translational activity --|GSK3b--|eIF2translational activity

  5. Negative controls on growth • AMPK • AMPAMPK TSC--|mTOR --|IRS1 GSK3b--|eIF2 • FOXO, esp FOXO3 • Oxidative/heat stress/Ppar-g  FOXO p27Kip--|cell cycle MuRF, atroginubiquitinylation myostatin (FOXO1) • TGF-b • TGFRSMADapoptosis, cell cycle arrest…

  6. Conditions that change growth • High force generation • Functional adequacy • Intrinsic force sensors • Damage • Nutrient/metabolite status – ATP/O2/Ca2+ • Stretch • Functional adequacy? • Force/deformation sensors? • Unloading • Functional superfluity

  7. Paracrine signaling • Prostaglandins • PGE2, PGF2a • Rapid activation, w/o upregulation of PLA2 • IGF-1 • Upregulated over hours • Distinct from endocrine IGF-1 or insulin • Myostatin • TGF-b member • Growth inhibitor

  8. 1.2 1.0 0.8 Glucose Insulin 0.6 Response Glucose uptake PI3K 0.4 p70S6k 0.2 Protein synthesis 0.0 0 5 10 15 20 25 30 -0.2 Time after exercise (h) Time course • Blood composition • Intracellular signaling • Protein synthesis • Sequential and slow Normalized response of several growth-related molecules after a single bout of resistance exercise Hernandez, et al., 2000

  9. Integrative control • Mechanical demand • FAK, Ca2+, other force sensors • Energetic demand • AMPK, GSK, Ragulator • Net growth of cell depends on balance • Overloaded, high energy cell grows • Overloaded, starved cell atrophies • Infrequent overload is sufficient to maintain or gain functional capacity • mTOR is a signal integrator

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