Haptoglobin Is Required to Prevent Oxidative Stress and Muscle Atrophy

被引:57
作者
Bertaggia, Enrico [1 ,2 ]
Scabia, Gaia [3 ]
Dalise, Stefania [4 ]
Lo Verso, Francesca [1 ,2 ]
Santini, Ferruccio [3 ]
Vitti, Paolo [3 ]
Chisari, Carmelo [4 ]
Sandri, Marco [1 ,2 ,5 ,6 ]
Maffei, Margherita [3 ,7 ]
机构
[1] Univ Padua, Dept Biomed Sci, Padua, Italy
[2] Venetian Inst Mol Med, Dulbecco Telethon Inst, Padua, Italy
[3] Univ Pisa, Dept Clin & Expt Med, Pisa, Italy
[4] Univ Hosp Pisa, Dept Neurosci, Unit Neurorehabil, Pisa, Italy
[5] CNR, Inst Neurosci, Padua, Italy
[6] Telethon Inst Genet & Med TIGEM, Naples, Italy
[7] CNR, Inst Clin Physiol, I-56100 Pisa, Italy
关键词
FOXO TRANSCRIPTION FACTORS; SKELETAL-MUSCLE; PROTEIN-DEGRADATION; IN-VIVO; AUTOPHAGY; DISEASE; PATHWAY; HYPERTROPHY; MECHANISMS; EXPRESSION;
D O I
10.1371/journal.pone.0100745
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Oxidative stress (OS) plays a major role on tissue function. Several catabolic or stress conditions exacerbate OS, inducing organ deterioration. Haptoglobin (Hp) is a circulating acute phase protein, produced by liver and adipose tissue, and has an important anti-oxidant function. Hp is induced in pro-oxidative conditions such as systemic inflammation or obesity. The role of systemic factors that modulate oxidative stress inside muscle cells is still poorly investigated. Results: We used Hp knockout mice (Hp(-/-)) to determine the role of this protein and therefore, of systemic OS in maintenance of muscle mass and function. Absence of Hp caused muscle atrophy and weakness due to activation of an atrophy program. When animals were stressed by acute exercise or by high fat diet (HFD), OS, muscle atrophy and force drop were exacerbated in Hp(-/-), Depending from the stress condition, autophagy-lysosome and ubiquitin-proteasome systems were differently induced. Conclusions: Hp is required to prevent OS and the activation of pathways leading to muscle atrophy and weakness in normal condition and upon metabolic challenges.
引用
收藏
页数:15
相关论文
共 45 条
[1]
Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo [J].
Bodine, SC ;
Stitt, TN ;
Gonzalez, M ;
Kline, WO ;
Stover, GL ;
Bauerlein, R ;
Zlotchenko, E ;
Scrimgeour, A ;
Lawrence, JC ;
Glass, DJ ;
Yancopoulos, GD .
NATURE CELL BIOLOGY, 2001, 3 (11) :1014-1019
[2]
Cellular and molecular mechanisms of muscle atrophy [J].
Bonaldo, Paolo ;
Sandri, Marco .
DISEASE MODELS & MECHANISMS, 2013, 6 (01) :25-39
[3]
The Nrf2 cell defence pathway: Keap1-dependent and -independent mechanisms of regulation [J].
Bryan, Holly K. ;
Olayanju, Adedamola ;
Goldring, Christopher E. ;
Park, B. Kevin .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (06) :705-717
[4]
Serum haptoglobin:: A novel marker of adiposity in humans [J].
Chiellini, C ;
Santini, F ;
Marsili, A ;
Berti, P ;
Bertacca, A ;
Pelosini, C ;
Scartabelli, G ;
Pardini, E ;
López-Soriano, J ;
Centoni, R ;
Ciccarone, AM ;
Benzi, L ;
Vitti, P ;
Del Prato, S ;
Pinchera, A ;
Maffei, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (06) :2678-2683
[5]
Obesity modulates the expression of haptoglobin in the white adipose tissue via TNFα [J].
Chiellini, C ;
Bertacca, A ;
Novelli, SE ;
Görgün, CZ ;
Ciccarone, A ;
Giordano, A ;
Xu, HY ;
Soukas, A ;
Costa, M ;
Gandini, D ;
Dimitri, R ;
Bottone, P ;
Cecchetti, P ;
Pardini, E ;
Perego, L ;
Navalesi, R ;
Folli, F ;
Benzi, L ;
Cinti, S ;
Friedman, JM ;
Hotamisligil, GS ;
Maffei, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 2002, 190 (02) :251-258
[6]
Correale Michele, 2012, Cardiovascular & Hematological Agents in Medicinal Chemistry, V10, P352
[7]
Della Gatta PA, 2014, BRAIN BEHAV IMMUN
[8]
Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity [J].
Dobrowolny, Gabriella ;
Aucello, Michela ;
Rizzuto, Emanuele ;
Beccafico, Sara ;
Mammucari, Cristina ;
Bonconpagni, Simona ;
Belia, Silvia ;
Wannenes, Francesca ;
Nicoletti, Carmine ;
Del Prete, Zaccaria ;
Rosenthal, Nadia ;
Molinaro, Mario ;
Protasi, Feliciano ;
Fano, Giorgio ;
Sandri, Marco ;
Musaro, Antonio .
CELL METABOLISM, 2008, 8 (05) :425-436
[9]
Dobryszycka W, 1997, EUR J CLIN CHEM CLIN, V35, P647
[10]
Vitamin E therapy results in a reduction in HDL function in individuals with diabetes and the haptoglobin 2-1 genotype [J].
Farbstein, Dan ;
Blum, Shany ;
Pollak, Mordechai ;
Asaf, Roy ;
Viener, Hilla Lee ;
Lache, Orit ;
Asleh, Rabea ;
Miller-Lotan, Rachel ;
Barkay, Ido ;
Star, Michael ;
Schwartz, Avery ;
Kalet-Littman, Shiri ;
Ozeri, David ;
Vaya, Jacob ;
Tavori, Hagai ;
Vardi, Moshe ;
Laor, Arie ;
Bucher, Stephen E. ;
Anbinder, Yefim ;
Moskovich, Doron ;
Abbas, Nur ;
Perry, Netta ;
Levy, Yishai ;
Levy, Andrew P. .
ATHEROSCLEROSIS, 2011, 219 (01) :240-244