1. Trang chủ
  2. » Y Tế - Sức Khỏe

Sarcopenia Age-Related Muscle Wasting and Weakness: Mechanisms and Treatments P30 potx

10 199 0
Tài liệu đã được kiểm tra trùng lặp

Đang tải... (xem toàn văn)

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Tiêu đề Sarcopenia Age-Related Muscle Wasting and Weakness: Mechanisms and Treatments
Tác giả K. O’Connell, Doran, Stamler, Vandervoort, Prochniewicz, Kayani, Neufer, Donoghue, Liu, Chung, Ng, McArdle, Broome, Soti
Trường học University of Example
Chuyên ngành Biomedical Sciences
Thể loại Bài luận
Năm xuất bản 2023
Thành phố Example City
Định dạng
Số trang 10
Dung lượng 1,64 MB

Các công cụ chuyển đổi và chỉnh sửa cho tài liệu này

Nội dung

In addition, increased concentrations of the ubiquitous small heat shock protein aB-crystallin were also detected by the proteomic profiling of senescent fibres Doran et al.. The age-dep

Trang 1

The chaperone cvHsp appears to counter-act deleterious protein aggregation in the cytosol, sarcolemma and actomyosin apparatus of aged muscle (Doran et al

2007c ) In addition, increased concentrations of the ubiquitous small heat shock protein aB-crystallin were also detected by the proteomic profiling of senescent fibres (Doran et al 2008 ) The family of small heat shock proteins quickly responds during stressful conditions and facilitates the disintegration of poly-disperse assemblies into smaller subunits This process is ATP-independent whereby small chaperone subunits bind to unfolding substrate and then reform into larger complexes (Stamler et al 2005 ) The age-dependent activation of the cytoprotective protein complement of skeletal muscles seems to counter-act increased levels of denatured proteins in senescent fibres, especially abundant elements such as non-functional myosins, actins, troponins and tropomysoins (Vandervoort 2002 ; Prochniewicz et al 2007 ) Increased chaperone levels repre-sent an esrepre-sential cellular rescue mechanism for eliminating the potentially destructive accumulation of inactive muscle protein aggregates During aging, adaptive fibre transformation occurs in skeletal muscles The fast-to-slow transi-tion process encompasses major cellular remodeling This includes the degenera-tion of the fastest-twitching fibre populadegenera-tion, the activadegenera-tion of the satellite pool of muscle precursor cells and a certain degree of phenotypic fibre shifting within a contractile unit However, since senescent muscles have a reduced regenerative capacity, adaptive fibre modulation probably triggers excessive detrimental pro-tein aggregation as compared to healthy adult tissues This in turn requires a massive cellular stress response to prevent contractile dysfunction Therefore, in the context of a blunted stress response involving large heat shock proteins in aged muscle (Kayani et al 2008 ), the drastic up-regulation of low-molecular-mass chaperones probably represents a compensatory mechanism that mostly supports filament remodeling (Doran et al 2007c ).

Continuous contractile activity clearly influences the expression of heat shock proteins (Neufer et al 1998 ) Key chaperones containing the a-crystallin domain are up-regulated following chronic contraction patterns (Donoghue et al 2007 ) In analogy to chronic neuromuscular activity, similar fibre transition processes occur

in aged muscle The concomitant damage to the actomyosin apparatus and associ-ated cytoskeletal network may therefore trigger an increased synthesis of small heat shock proteins (Doran et al 2009a ) In contrast, cellular stress does not generate a sufficient response by larger heat shock proteins, such as those encoded by the Hsp70 gene (Liu et al 2006 ) The up-regulation of Hsp70 and related chaperones

is usually part of a highly coordinated stress response that prevents extensive mus-cular atrophy by limiting the stress-induced rate of cellular degeneration (Chung and Ng 2006 ) High levels of Hsp70 are essential for the stabilization of metabolic pathways, the prevention of high rates of apoptosis and the facilitation of physio-logical adaptation to changed functional demands An age-related impairment of the Hsp70 response is believed to play a key role in contractile deficits (McArdle

et al 2004 ) It is therefore not surprising that skeletal muscles of aged transgenic mice with over-expressed levels of Hsp70 are partially protected against fibre degeneration (Broome et al 2006 ).

Trang 2

This suggests that a well-designed pharmacological approach to enhance the natural stress response could potentially eliminate excessive fibre damage in aged muscle In other areas of biomedicine, the drug-induced modulation of the cellular stress response has already gained considerable attention, as reviewed by Soti et al ( 2005 ) Various inducers, co-inducers and inhibitors of specific heat shock proteins are currently evaluated as emerging therapeutic vehicles for the treatment of heart disease, diabetes, cancer and neurodegenerative disorders (Calderwood et al 2006 ; Shamaei-Tousi et al 2007 ) Since the up-regulation of small heat shock proteins, such as aB-crystallin or cvHsp, may represent an auto-protective mechanism in senescent muscle, a further increase in their expression levels may have therapeutic benefits Hence, a pharmacologically mediated increase in essential muscle chap-erones may be a realistic treatment option for eliminating certain neuromuscular impairments and could decisively improve the survival rate of stressed motor units

in the senescent body.

3.4 Excitation–Contraction Uncoupling in Aged Muscle

Ca2+-fluxes represent one of the most crucial second messenger system in contrac-tile tissues (Berchtold et al 2000 ) Alterations in Ca2+-levels do not only affect protein activity and key physiological processes, but also gene expression patterns

in skeletal muscle Changes in the cytosolic Ca2+-concentration play a key role in myogenesis, differentiation, fibre transformation, metabolic regulation, excitation– contraction coupling and muscle relaxation Importantly, cyclic alterations in cyto-solic Ca2+-levels determine the contractile status of skeletal muscle fibres The regulation of Ca2+-homoeostasis and the mediation of the excitation–contraction– relaxation cycle depend on a finely tuned interplay between voltage-sensing recep-tors in the transverse tubules, Ca2+-release channel units in the junctional sarcoplasmic reticulum, luminal and cytosolic Ca2+-binding proteins, and Ca2+ -pumps of the sarcoplasmic reticulum, as well as minor structural components of the triad junction and sarcolemmal ion-regulatory elements such as ion exchangers and ion pumps (Murray et al 1998 ) It is therefore not surprising that abnormal Ca2+ -handling is involved in a variety of muscle pathologies (MacLennan 2000 ; Froemming and Ohlendieck 2001 ), including sarcopenia of old age (Renganathan

et al 1997 ; O’Connell et al 2008 b).

The physical coupling between the voltage-sensing a1S-subunit of the trans-verse-tubular dihydropyridine receptor and the ryanodine receptor Ca2+-release channel of the junctional sarcoplasmic reticulum forms the central signal transduc-tion unit during excitatransduc-tion–contractransduc-tion coupling in mature skeletal muscles (MacLennan et al 2002 ) The dihydropyridine receptor from skeletal muscle con-sists of a a1S-a2/d-b-g configuration The a1S-subunit represents the principal ion channel pore with three cytoplasmic loops between four repeat segments, whereby the II-III loop domain interacts directly with the junctional calcium release channel During muscle aging, a drastically lowered supply of Ca2+-ions to contractile

Trang 3

proteins occurs due to uncoupling between the two main triad receptors (Renganathan et al 1997 ) Excitation–contraction uncoupling appears to be due to

a larger number of ryanodine receptors being uncoupled to the voltage-sensing dihydropyridine receptor units as compared to mature fibres A pathophysiological disconnection between sarcolemmal excitation and muscle contraction may result

in alterations in the voltage-gated Ca2+-release mechanism, decreases in myoplas-mic Ca2+-elevation in response to surface depolarisation, reduced Ca2+-supply to the actomyosin apparatus and reduced contractile strength Thus, abnormal Ca2+ -handling may account for a significant proportion of the decay in skeletal muscle force during aging (Delbono et al 1995 ) A recent immunoblotting and immuno-fluorescence survey has confirmed the excitation–contraction coupling hypothesis The Ca2+-binding protein named sarcalumenin, which represents a major mediator

of ion shuttling within the longitudinal sarcoplasmic reticulum, was shown to be greatly reduced in aged rat gastrocnemius muscle as compared to young adult specimens (O’Connell et al 2008 b) In addition, key elements of the plasmalemma-associated Ca2+-extrusion system, i.e the calmodulin-dependent Ca2+-ATPase and the Na+-Ca2+-exchanger, were also found to be diminished in aged muscle.

Figure 4 summarizes the findings of the immunoblotting survey of essential physi-ological regulators of Ca2+-homeostasis and how their dysregulation may affect the excitation–contraction–relaxation cycle during aging The overall protein band pat-tern of electrophoretically separated crude tissue extracts from 3-month versus 30-month old rat gastrocnemius muscle was very comparable between young adult versus senescent fibres The previously reported senescence-related decrease in the

a1S-subunit of the dihydropryridine receptor, but not its auxiliary a2-subunit, was confirmed Immunoblotting of the sarcoplasmic reticulum proteins that mediate Ca2+ -buffering and Ca2+-removal, i.e fast and slow calsequestrins and the Ca2+-pumping ATPase isoforms SERCA1 and SERCA2, suggested a shift to a slower phenotype, but these findings are not statistically significant In contrast, the reduced expression of the 160 kDa Ca2+-binding protein sarcalumenin and its related glycoprotein product

of 53 kDa, as well as the Na+-Ca2+-exchanger and the PMCA-type Ca2+-ATPase was shown to be significant in aged muscle Thus, downstream from the coupling defect between the dihydropyridine receptor and the junctional Ca2+-release channel, addi-tional age-dependent changes appear to exist in Ca2+-regulatory elements Reduced levels of sarcalumenin and the two sarcolemmal Ca2+-extrusion proteins may cause abnormal luminal Ca2+-binding and impaired Ca2+-removal (O’Connell et al 2008 b) This in turn could exacerbate disturbed ion fluxes and diminished triad signaling in senescent muscle and thereby contribute to contractile weakness.

4 Conclusion

Natural aging is a fundamental biological process The functional decline of skeletal muscle fibres and the loss of total muscle mass are crucial factors that render the human body more susceptible to a metabolic disequilibrium and physical

Trang 4

weakness Besides studying the histological and anatomical effects of muscle aging

on frailty and fragility, it is also crucial to determine the molecular mechanisms that underlie age-dependent alterations at the cellular level The application of modern proteomic methodology for analysing age-related impairments in contractile tissues promises to elucidate the pathobiochemical processes that lead to sarcopenia of old age Mass spectrometry represents an unrivalled technique for the swift and reliable identification of protein factors involved in pathological pathways or compensatory

Fig 4 Overview of the excitation–contraction uncoupling hypothesis of skeletal muscle aging and comparative immunoblot analysis of key Ca2+-handling proteins in young adult versus senescent muscle Shown is a Coomassie-stained gel and immunoblots of young adult versus aged rat gastrocnemius preparations Immunoblots were labeled with antibodies to key proteins of the sarcolemma (SL), transverse tubules (TT) and sarcoplasmic reticulum (SR), including sarcalumenin (SAR) and its alternative splice product, the 53 kDa sarcoplasmic reticulum glycoprotein (53-SRGP), fast and slow calsequsetrin (fast CSQf; slow CSQs), fast and slow sarcoplasmic reticulum

Ca2+-ATPase (fast SERCA1; slow SERCA2), the Na+-Ca2+-exchanger (NCX), the plasmalemmal

Ca2+-ATPase (PMCA), and the a1S- and a2-subunit of the dihydropryridine receptor (DHPR) Molecular mass standards (in kDa) are indicated on the left of the Coomassie-stained gel panel

The comparative blotting was statistically evaluated using an unpaired Student’s t-test (n = 6;

*p < 0.05; **p < 0.01 Standard methods were employed for muscle preparations from crude tissue extracts, one-dimensional gel electrophoresis and immunoblot analysis of Ca2+-handling proteins (O’Connell et al 2007) The central panel outlines the dysregulation of Ca2+-fluxes in senescent fibres and how this may affect the excitation–contraction–relaxation cycle during skeletal muscle aging Besides the Ca2+-handling proteins that have been analysed by immunoblotting, other key elements of ion homeostasis and muscle regulation are included in this diagram, i.e the ryanodine receptor (RyR) Ca2+-release channel of the sarcoplasmic reticulum and the troponin subunit TnC

Trang 5

mechanisms involved in aging Over the last few years, mass spectrometry-based proteomics has identified a large number of relatively sarcopenia-specific biomark-ers Skeletal muscle proteins that exhibit altered expression levels or changed post-translational modifications during aging include regulatory proteins, contractile elements, metabolic enzymes and cellular stress proteins The complexity of the observed changes in the senescent muscle proteome confirm the idea that sarcope-nia is probably based on a multi-factorial etiology, rather than alterations in just one class of protein factors, regulatory mechanisms or aging-inducing gene clusters Proteomic profiling studies have established distinct switches in fibre type-specific isoforms of contractile and metabolic proteins during aging, demonstrating an age-related transformation to slower-twitching muscles The fast-to-slow transition process is accompanied by bioenergetic adaptation mechanisms The comparative proteomic analysis of adult versus senescent muscles has clearly revealed a drastic shift to more aerobic-oxidative metabolism during aging The proteomic identifica-tion of new sarcopenic biomarkers and their detailed cell biological, physiological and biochemical characterzation will hopefully lead to the prompt development of superior diagnostic tools and the improved design of pharmacological strategies to counter-act the age-induced loss of contractile tissue Since alterations in the neu-romuscular system are of central importance for comprehending the overall patho-genesis of the aging process in humans, the recent findings from proteomic studies will be crucial for improving our general biomedical knowledge on the mechanisms

of aging.

Acknowledgements Research in the author’s laboratory was supported by a principal investiga-tor grant from Science Foundation Ireland (SFI-04/IN3/B614) and equipment grants from the Irish Health Research Board (HRB-EQ/2003/3, HRB-EQ/2004/2) and the Higher Education Authority (HEA-RERGS-07-NUIM) The authors thank Dr Marina Lynch (Trinity College Dublin) for her generous help obtaining aged rat muscle, and Ms Caroline Batchlor (NUI Maynooth) for assis-tance with mass spectrometry

References

Adams, G R & Vaziri, N D (2006) Skeletal muscle dysfunction in chronic renal failure: effects

of exercise The American Journal of Physiology, 290, F753–F761.

Aebersold, R & Mann, M (2003) Mass spectrometry-based proteomics Nature, 422, 198–207.

Aggarwal, K & Lee, K H (2003) Functional genomics and proteomics as a foundation for

sys-tems biology Briefings in Functional Genomics & Proteomics, 2, 175–184.

Amin, J., Ananthan, J., Voellmy, R (1988) Key features of heat shock regulatory elements

Molecular and Cellular Biology, 8, 3761–3769.

Anckar, J & Sistonen, L (2007) Heat shock factor 1 as a coordinator of stress and developmental

pathways Advances in Experimental Medicine and Biology, 594, 78–88.

Anderson, N L & Anderson, N G (2002) The human plasma proteome: history, character, and

diagnostic prospects Molecular & Cellular Proteomics, 1, 845–867.

Balagopal, P., Rooyackers, O E., Adey, D B., Ades, P A., Nair, K S (1997) Effects of aging on

in vivo synthesis of skeletal muscle myosin heavy-chain and sarcoplasmic protein in humans

The American Journal of Physiology, 273, E790–E800.

Trang 6

Baumgartner, R N., Stauber, P M., McHugh, D., Koehler, K M., Garry, P J (1995) Cross-sectional

age differences in body composition in persons 60+ years of age Journal of Gerontology

A Biological Sciences and Medical Sciences, 50, M307–M316.

Berchtold, M W., Brinkmeier, H., Muntener, M (2000) Calcium ion in skeletal muscle: its crucial

role for muscle function, plasticity, and disease Physiological Reviews, 80, 1215–1265.

Bosworth, C A., Chou, C W., Cole, R B., Rees, B B (2005) Protein expression patterns in zebrafish skeletal muscle: initial characterization and the effects of hypoxic exposure

Proteomics, 5, 1362–1371.

Bouley, J., Meunier, B., Chambon, C., De Smet, S., Hocquette, J F., Picard, B (2005) Proteomic

analysis of bovine skeletal muscle hypertrophy Proteomics, 5, 490–500.

Bozzo, C., Spolaore, B., Toniolo, L., Stevens, L., Bastide, B., Cieniewski-Bernard, C., Fontana, A., Mounier, Y., Reggiani, C (2005) Nerve influence on myosin light chain phosphorylation in

slow and fast skeletal muscles The FEBS Journal, 272, 5771–5785.

Broome, C S., Kayani, A C., Palomero, J., Dillmann, W H., Mestril, R., Jackson, M J., McArdle, A (2006) Effect of lifelong overexpression of HSP70 in skeletal muscle on age-related oxidative

stress and adaptation after nondamaging contractile activity The FASEB Journal, 20,

1549–1551

Burniston, J G (2008) Changes in the rat skeletal muscle proteome induced by

moderate-inten-sity endurance exercise Biochimica et Biophysica Acta, 1784, 1077–1086.

Calderwood, S K., Khaleque, M A., Sawyer, D B., Ciocca, D R (2006) Heat shock proteins in

cancer: chaperones of tumorigenesis Trends in Biochemical Sciences, 31, 164–172.

Canas, B., Lopez-Ferrer, D., Ramos-Fernandez, A., Camafeita, E., Calvo, E (2006) Mass

spectrom-etry technologies for proteomics Briefings in Functional Genomics & Proteomics, 4, 295–320.

Capitanio, D., Vasso, M., Fania, C., Moriggi, M., Vigano, A., Procacci, P., Magnaghi, V., Gelfi, C (2009) Comparative proteomic profile of rat sciatic nerve and gastrocnemius muscle tissues

in ageing by 2-D DIGE Proteomics, 9, 2004–2020.

Carlson, B M (2004) Denervation and the aging of skeletal muscle Basic and Applied Myology,

14, 135–140.

Chan, K M., Doherty, T J., Brown, W F (2001) Contractile properties of human motor units in

health, aging, and disease Muscle & Nerve, 24, 1113–1133.

Chung, L & Ng, Y C (2006) Age-related alterations in expression of apoptosis regulatory

pro-teins and heat shock propro-teins in rat skeletal muscle Biochimica et Biophysica Acta, 1762,

103–109

Clark, K A., McElhinny, A S., Beckerle, M C., Gregorio, C C (2002) Striated muscle

cyto-architecture: an intricate web of form and function Annual Review of Cell and Developmental Biology, 18, 637–706.

Dalla Libera, L., Vescovo, G., Volterrani, M (2008) Physiological basis for contractile

dysfunc-tion in heart failure Current Pharmaceutical Design, 14, 2572–2581.

Degens, H (1998) Age-related changes in the microcirculation of skeletal muscle Advances in Experimental Medicine and Biology, 454, 343–348.

de Hoog, C L & Mann, M (2004) Proteomics Annual Review of Genomics and Human Genetics, 5, 267–293.

Delbono, O., O’Rourke, K S., Ettinger, W H (1995) Excitation-calcium release uncoupling in

aged single human skeletal muscle fibers The Journal of Membrane Biology, 148, 211–222.

Dencher, N A., Frenzel, M., Reifschneider, N H., Sugawa, M., Krause, F (2007) Proteome

alterations in rat mitochondria caused by aging Annals of the New York Academy of Sciences,

1100, 291–298.

Dencher, N A., Goto, S., Reifschneider, N H., Sugawa, M., Krause, F (2006) Unraveling

age-dependent variation of the mitochondrial proteome Annals of the New York Academy of Sciences, 1067, 116–119.

Dennis, R A., Przybyla, B., Gurley, C., Kortebein, P M., Simpson, P., Sullivan, D H., Peterson,

C A (2008) Aging alters gene expression of growth and remodeling factors in human skeletal

muscle both at rest and in response to acute resistance exercise Physiological Genomics, 32,

393–400

Trang 7

De Palma, S., Morandi, L., Mariani, E., Begum, S., Cerretelli, P., Wait, R., Gelfi, C (2006)

Proteomic investigation of the molecular pathophysiology of dysferlinopathy Proteomics, 6,

379–385

De Palma, S., Ripamonti, M., Vigano, A., Moriggi, M., Capitanio, D., Samaja, M., Milano, G., Cerretelli, P., Wait, R., Gelfi, C (2007) Metabolic modulation induced by chronic hypoxia in

rats using a comparative proteomic analysis of skeletal muscle tissue Journal of Proteome Research, 6, 1974–1984.

Dirks, A & Leeuwenburgh, C (2002) Apoptosis in skeletal muscle with aging The American Journal of Physiology, 282, R519–R527.

Doherty, T J (2003) Aging and sarcopenia Journal of Applied Physiology, 95, 1717–1727.

Doherty, M K., McLean, L., Hayter, J R., Pratt, J M., Robertson, D H., El, S A (2004) The proteome of chicken skeletal muscle: changes in soluble protein expression during growth in

a layer strain Proteomics, 4, 2082–2093.

Domon, B & Aebersold, R (2006) Mass spectrometry and protein analysis Science, 312,

212–217

Donoghue, P., Doran, P., Dowling, P., Ohlendieck, K (2005) Differential expression of the fast

skeletal muscle proteome following chronic low-frequency stimulation Biochimica et Biophysica Acta, 1752, 166–176.

Donoghue, P., Doran, P., Wynne, K., Pedersen, K., Dunn, M J., Ohlendieck, K (2007) Proteomic

profiling of chronic low-frequency stimulated fast muscle Proteomics, 7, 3417–3430.

Doran, P., Martin, G., Dowling, P., Jockusch, H., Ohlendieck, K (2006) Proteome analysis of the dystrophin-deficient MDX diaphragm reveals a drastic increase in the heat shock protein

cvHSP Proteomics, 6, 4610–4621.

Doran, P., Donoghue, P., O’Connell, K., Gannon, J., Ohlendieck, K (2007a) Proteomic profiling

of pathological and aged skeletal muscle fibres by peptide mass fingerprinting International Journal of Molecular Medicine, 19, 547–564.

Doran, P., Gannon, J., O’Connell, K., Ohlendieck, K (2007b) Proteomic profiling of animal models

mimicking skeletal muscle disorders Proteomics: Clinical Applications, 1, 1169–1184.

Doran, P., Gannon, J., O’Connell, K., Ohlendieck, K (2007c) Aging skeletal muscle shows a drastic increase in the small heat shock proteins aB-crystallin/HspB5 and cvHsp/HspB7

European Journal of Cell Biology, 86, 629–640.

Doran, P., O’Connell, K., Gannon, J., Kavanagh, M., Ohlendieck, K (2008) Opposite pathobio-chemical fate of pyruvate kinase and adenylate kinase in aged rat skeletal muscle as revealed

by proteomic DIGE analysis Proteomics, 8, 364–377.

Doran, P., Donoghue, P., O’Connell, K., Gannon, J., Ohlendieck, K (2009a) Proteomics of

skel-etal muscle aging Proteomics, 9, 989–1003.

Doran, P., Wilton, S D., Fletcher, S., Ohlendieck, K (2009b) Proteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx

diaphragm Proteomics, 9, 671–685.

Duan, X., Berthiaume, F., Yarmush, D., Yarmush, M L (2006) Proteomic analysis of altered protein expression in skeletal muscle of rats in a hypermetabolic state induced by burn sepsis

The Biochemical Journal, 397, 149–158.

Edstrom, E., Altun, M., Bergman, E., Johnson, H., Kullberg, S., Ramirez-Leon, V., Ulfhake, B (2007) Factors contributing to neuromuscular impairment and sarcopenia during aging

Physiology & Behavior, 92, 129–135.

Ellis, R J & van der Vies, S M (1991) Molecular chaperones Annual Review of Biochemistry,

60, 321–347.

Emery, A & Muntoni, F (2003) Duchenne muscular dystrophy (3rd ed., pp 1–270) Oxford, UK:

Oxford University Press

Faulkner, J A., Larkin, L M., Claflin, D R., Brooks, S V (2007) Age-related changes in the

structure and function of skeletal muscles Clinical and Experimental Pharmacology & Physiology, 34, 1091–1096.

Feng, J., Xie, H., Meany, D L., Thompson, L V., Arriaga, E A., Griffin, T J (2008) Quantitative proteomic profiling of muscle type-dependent and age-dependent protein carbonylation in rat

Trang 8

skeletal muscle mitochondria Journal of Gerontology A Biological Sciences and Medical Sciences, 63, 1137–1152.

Fenn, J B., Mann, M., Meng, C K., Wong, S F., Whitehouse, C M (1989) Electrospray

ioniza-tion for mass spectrometry of large biomolecules Science, 246, 64–71.

Ferguson, P L & Smith, R D (2003) Proteome analysis by mass spectrometry Annual Review

of Biophysics and Biomolecular Structure, 32, 399–424.

Figueiredo, P A., Mota, M P., Appell, H J., Duarte, J A (2008) The role of mitochondria in

aging of skeletal muscle Biogerontology, 9, 67–84.

Fitts, R H (2008) The cross-bridge cycle and skeletal muscle fatigue Journal of Applied Physiology, 104, 551–558.

Flueck, M & Hoppeler, H (2003) Molecular basis of skeletal muscle plasticity: from gene to

form and function Reviews of Physiology Biochemistry and Pharmacology, 146,

159–216

Forbes, G B & Reina, J C (1970) Adult lean body mass declines with age: some longitudinal

observations Metabolism, 19, 653–663.

Forner, F., Foster, L J., Campanaro, S., Valle, G., Mann, M (2006) Quantitative proteomic

com-parison of rat mitochondria from muscle, heart, and liver Molecular & Cellular Proteomics,

5, 608–619.

Froemming, G R & Ohlendieck, K (2001) Role of ion-regulatory membrane proteins in

inher-ited muscle diseases Frontiers in Bioscience, 6, D65–D74.

Froemming, G R., Murray, B E., Harmon, S., Pette, D., Ohlendieck, K (2000) Comparative analysis of the isoform expression pattern of Ca2+-regulatory membrane proteins in fast-twitch,

slow-twitch, cardiac, neonatal and chronic low-frequency stimulated muscle fibres Biochimica

et Biophysica Acta, 1466, 151–168.

Frontera, W R., Reid, K F., Phillips, E M., Krivickas, L S., Hughes, V A., Roubenoff, R., Fielding, R A (2008) Muscle fiber size and function in elderly humans: a longitudinal study

Journal of Applied Physiology, 105, 637–642.

Gannon, J., Staunton, L., O’Connell, K., Doran, P., Ohlendieck, K (2008) Phosphoproteomic

analysis of aged skeletal muscle International Journal of Molecular Medicine, 22, 33–42.

Gelfi, C., De Palma, S., Cerretelli, P., Begum, S., Wait, R (2003) Two-dimensional protein map

of human vastus lateralis muscle Electrophoresis, 24, 286–295.

Gelfi, C., Vigano, A., De Palma, S., Ripamonti, M., Begum, S., Cerretelli, P., Wait, R (2006a) 2-D protein maps of rat gastrocnemius and soleus muscles: a tool for muscle plasticity

assess-ment Proteomics, 6, 321–340.

Gelfi, C., Vigano, A., Ripamonti, M., Pontoglio, A., Begum, S., Pellegrino, M A., Grassi, B.,

Bottinelli, R., Wait, R., Cerretelli, P (2006b) The human muscle proteome in aging Journal

of Proteome Research, 5, 1344–1353.

Giresi, P G., Stevenson, E J., Theilhaber, J., Koncarevic, A., Parkington, J., Fielding, R A.,

Kandarian, S C (2005) Identification of a molecular signature of sarcopenia Physiological Genomics, 21, 253–263.

Golenhofen, N., Perng, M D., Quinlan, R A., Drenckhahn, D (2004) Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal

muscle Histochemistry and Cell Biology, 122, 415–425.

Gonnet, F., Bouazza, B., Millot, G A., Ziaei, S., Garcia, L., Butler-Browne, G S., Mouly, V., Tortajada, J., Danos, O., Svinartchouk, F (2008) Proteome analysis of differentiating human

myoblasts by dialysis-assisted two-dimensional gel electrophoresis (DAGE) Proteomics, 8,

264–278

Gordon, A M., Homsher, E., Regnier, M (2000) Regulation of contraction in striated muscle

Physiological Reviews, 80, 853–924.

Gorg, A., Weiss, W., Dunn, M J (2004) Current two-dimensional electrophoresis technology for

proteomics Proteomics, 4, 3665–3685.

Hamelin, M., Sayd, T., Chambon, C., Bouix, J., Bibé, B., Milenkovic, D., Leveziel, H., Georges, M., Clop, A., Marinova, P., Laville, E (2006) Proteomic analysis of ovine muscle hypertrophy

Journal of Animal Science, 84, 3266–3276.

Trang 9

Hamelin, M., Sayd, T., Chambon, C., Bouix, J., Bibe, B., Milenkovic, D., Leveziel, H., Georges, M., Clop, A., Marinova, P., Laville, E (2007) Differential expression of sarcoplasmic proteins in

four heterogeneous ovine skeletal muscles Proteomics, 7, 271–280.

Isfort, R J (2002) Proteomic analysis of striated muscle Journal of Chromatography, B771,

155–165

Isfort, R J., Hinkle, R T., Jones, M B., Wang, F., Greis, K D., Sun, Y., Keough, T W., Anderson, N L., Sheldon, R J (2000) Proteomic analysis of the atrophying rat soleus muscle following

den-ervation Electrophoresis, 21, 2228–2234.

Janssen, I., Heymsfield, S B., Ross, R (2002) Low Relative Skeletal Muscle Mass (Sarcopenia)

in Older Persons Is Associated with Functional Impairment and Physical Disability Journal of the American Geriatrics Society, 50, 889–896.

Jia, X., Hildrum, K I., Westad, F., Kummen, E., Aass, L., Hollung, K (2006) Changes in enzymes associated with energy metabolism during the early post mortem period in

longissi-mus thoracis bovine longissi-muscle analyzed by proteomics Journal of Proteome Research, 5,

1763–1769

Kandarian, S C & Jackman, R W (2006) Intracellular signaling during skeletal muscle atrophy

Muscle & Nerve, 33, 155–65.

Kanski, J., Hong, S J., Schoneich, C (2005) Proteomic analysis of protein nitration in aging skeletal muscle and identification of nitrotyrosine-containing sequences in vivo by

nanoelec-trospray ionization tandem mass spectrometry The Journal of Biological Chemistry, 280,

24261–24266

Kaufmann, M., Simoneau, J A., Veerkamp, J H., Pette, D (1989) Electrostimulation-induced increases in fatty acid-binding protein and myoglobin in rat fast-twitch muscle and comparison

with tissue levels in heart FEBS Letters, 245, 181–184.

Kayani, A C., Morton, J P., McArdle, A (2008) The exercise-induced stress response in skeletal

muscle: failure during aging Applied Physiology, Nutrition, and Metabolism, 33,

1033–1041

Kayo, T., Allison, D B., Weinbruch, R., Prolla, T A (2001) Influences of aging and caloric

restriction on the transcriptional profile of skeletal muscle from rhesus monkeys Proceedings

of the National Academy of Science USA, 98, 5093–5098.

Kim, N K., Joh, J H., Park, H R., Kim, O H., Park, B Y., Lee, C S (2004) Differential expres-sion profiling of the proteomes and their mRNAs in porcine white and red skeletal muscles

Proteomics, 4, 3422–3428.

Kislinger, T., Gramolini, A O., Pan, Y., Rahman, K., MacLennan, D H., Emili, A (2005)

Proteome dynamics during C2C12 myoblast differentiation Molecular & Cellular Proteomics,

4, 887–901.

Kreutziger, K L., Gillis, T E., Davis, J P., Tikunova, S B., Regnier, M (2007) Influence of enhanced troponin C Ca2+-binding affinity on cooperative thin filament activation in rabbit

skeletal muscle The Journal of Physiology, 583, 337–350.

Lametsch, R., Bendixen, E (2001) Proteome analysis applied to meat science: characterizing

postmortem changes in porcine muscle Journal of Agriculture and Food Chemistry, 49,

4531–4537

Le Bihan, M C., Hou, Y., Harris, N., Tarelli, E., Coulton, G R (2006) Proteomic analysis of fast and slow muscles from normal and kyphoscoliotic mice using protein arrays, 2-DE and MS

Proteomics, 6, 4646–4661.

Lee, C E., McArdle, A., Griffiths, R D (2007) The role of hormones, cytokines and heat shock

proteins during age-related muscle loss Clinical Nutrition, 26, 524–534.

Lindle, R S., Metter, E J., Lynch, N A., Fleg, J L., Fozard, J L., Tobin, L (1997) Age and

gender comparisons of muscle strength in 654 women and men aged 20-93 yr Journal of Applied Physiology, 83, 1581–1587.

Liu, Y., Gampert, L., Nething, K., Steinacker, J M (2006) Response and function of skeletal

muscle heat shock protein 70 Frontiers in Bioscience, 11, 2802–2827.

Lombardi, A., Silvestri, E., Cioffi, F., Senese, R., Lanni, A., Goglia, F., de Lange, P., Moreno, M (2009) Defining the transcriptomic and proteomic profiles of rat ageing skeletal muscle by the

Trang 10

use of a cDNA array, 2D- and Blue native-PAGE approach Journal of Proteomics, 72,

708–721

Lynch, G S., Schertzer, J D., Ryall, J G (2007) Therapeutic approaches for muscle wasting

disorders Pharmacology & Therapeutics, 113, 461–487.

MacLennan, D H (2000) Ca2+ signalling and muscle disease European Journal of Biochemistry,

267, 5291–5297.

MacLennan, D H., Abu-Abed, M., Kang, C (2002) Structure-function relationships in Ca(2+)

cycling proteins Journal of Molecular and Cellular Cardiology, 34, 897–918.

Marouga, R., David, S., Hawkins, E (2005) The development of the DIGE system: 2D

fluores-cence difference gel analysis technology Analytical and Bioanalytical Chemistry, 382,

669–678

McArdle, A & Jackson, M J (2000) Exercise, oxidative stress and ageing Journal of Anatomy,

197, 539–541.

McArdle, A., Dillmann, W H., Mestril, R., Faulkner, J A., Jackson, M J (2004) Overexpression

of HSP70 in mouse skeletal muscle protects against muscle damage and age-related muscle

dysfunction The FASEB Journal, 18, 355–357.

Meany, D L., Xie, H., Thompson, L V., Arriaga, E A., Griffin, T J (2007) Identification of carbonylated proteins from enriched rat skeletal muscle mitochondria using affinity

chroma-tography-stable isotope labeling and tandem mass spectrometry Proteomics, 7, 1150–1163.

Melstrom, L G., Melstrom, K A., Ding, X Z., Adrian, T E (2007) Mechanisms of skeletal

muscle degradation and its therapy in cancer cachexia Histology and Histopathology, 22,

805–814

Melton, L J., Khosla, S., Crowson, C S., O’Connor, M K., O’Fallon, W M., Riggs, B L (2000)

Epidemiology of sarcopenia Journal of the American Geriatrics Society, 48, 625–630.

Munoz, M E & Ponce, E (2003) Pyruvate kinase: current status of regulatory and functional

properties Comparative Biochemistry and Physiology Part B: Biochemistry & Molecular Biology, 135, 197–218.

Murray, B E., Froemming, G R., Maguire, P B., Ohlendieck, K (1998) Excitation– contraction–relaxation cycle: role of Ca2+-regulatory membrane proteins in normal, stimulated

and pathological skeletal muscle (review) International Journal of Molecular Medicine, 1,

677–687

Neufer, P D., Ordway, G A., Williams, R S (1998) Transient regulation of c-fos, alpha

B-crystallin, and hsp70 in muscle during recovery from contractile activity The American Journal of Physiology, 274, C341–C346.

Nicholl, I D & Quinlan, R A (1994) Chaperone activity of alpha-crystallins modulates

inter-mediate filament assembly The EMBO Journal, 13, 945–953.

Nishimura, R N & Sharp, F R (2005) Heat shock proteins and neuromuscular disease Muscle & Nerve, 32, 693–709.

O’Connell, K., Gannon, J., Doran, P., Ohlendieck, K (2007) Proteomic profiling reveals a

severely perturbed protein expression pattern in aged skeletal muscle International Journal of Molecular Medicine, 20, 145–153.

O’Connell, K., Doran, P., Gannon, J., Ohlendieck, K (2008a) Lectin-based proteomic profiling

of aged skeletal muscle: Decreased pyruvate kinase isozyme M1 exhibits drastically increased

levels of N-glycosylation European Journal of Cell Biology, 87, 793–805.

O’Connell, K., Gannon, J., Doran, P., Ohlendieck, K (2008b) Reduced expression of

sarcalu-menin and related Ca2+ -regulatory proteins in aged rat skeletal muscle Experimental Gerontology, 43, 958–961.

Okumura, N., Hashida-Okumura, A., Kita, K., Matsubae, M., Matsubara, T., Takao, T., Nagai, K

(2005) Proteomic analysis of slow- and fast-twitch skeletal muscles Proteomics, 5,

2896–2906

Pette, D (2001) Historical Perspectives: plasticity of mammalian skeletal muscle Journal of Applied Physiology, 90, 1119–1124.

Pette, D & Staron, R S (1990) Cellular and molecular diversities of mammalian skeletal muscle

fibers Reviews of Physiology Biochemistry and Pharmacology, 116, 1–76.

Ngày đăng: 07/07/2014, 10:20

TỪ KHÓA LIÊN QUAN

🧩 Sản phẩm bạn có thể quan tâm