full text - Akademia Wychowania Fizycznego w Krakowie

Wanda Pilch, Anna Piotrowskaukładu hormonalnego oraz immunologicznego przedstawianązazwyczaj w postaci krzywej typu Gaussa(krzywa dzwonowa), co oznacza, że zbyt mała aktywnośćfizyczna jest słabym bodźcem prozdrowotnym,a zbyt duża aktywność może stać się zjawiskiem niekorzystnym.Mechanizm zachodzących wówczas zmianna poziomie komórki tłumaczony jest teorią hormezy.Umiarkowany stres wysiłkowy wywołany w różnegotypu komórkach może prowadzić do zmniejszenia ichuszkodzeń i poprawy przeżycia w porównaniu z działaniemna nie stresu ostrego [58].PIŚMIENNICTWO • LITERATURE[1] Ritossa F: A new paffing pattern induced by temperatureshock and DNP in Drosophila melanogaster. Experientia,1962; 18: 571–573.[2] Morimoto RI: Regulation of the heat shock transcriptionalresponse; cross talk between a family of heat shockfactors, molecular chaperones, and negative regulators.Genes Dev, 1998;12: 3788–3796.[3] Lanneau D, Brunet M, Frisan E, Solary E, FontenayM, Garrido C: Heat shock proteins: essential proteinsfor apoptosis regulation. J Cell Mol Med, 2008; 12:743–761.[4] Binder RJ, Vatner R, Srivastava P: The heat-shock proteinreceptors: some answers and more questions. TissueAntigens, 2004; 64: 442–451.[5] Schmitt E, Gehrmann M, Brunet M, Multhoff G, GarridoC: Intracellular and extracellular functions of heat shockproteins: repercussions in cancer therapy. J Leukoc Biol,2007; 81: 15–27.[6] Kiliańska ZM: Apoptoza organizmów zwierzęcych;w Kłyszejko-Stefanowicz L (red.): Cytobiochemia.Warszawa, Wydawnictwo Naukowe PWN, 2002: 772–815.[7] Cymerys J, Niemiałtowski M: Białka szoku cieplnego –molekularne perpetum mobile. Post Biol Kom, 2004; 31:331–352.[8] Arbeiter K, Bidmon B , Endemann M, Onno BenderT, Eickelberg O, Ruffingshofer D, Mueller T, Regele H ,Herkner K Aufricht C: Peritoneal dialysate fluid compositiondetermines heat shock protein expression patterns inhuman mesothelial cells. Kidney International, 2001; 60,1930–1937.[9] Kalinowska M, Garncarz W, Pietrowska M, Garrard WT,Widlak P: Regulation of the human apoptotic DNase/RNase endonuclease G: involvement of Hsp70 and ATP.Apoptosis, 2005; 10: 821–830.[10] Sakahira H, Nagata S: Co-transnational folding of caspase-activatedDNase with Hsp70, Hsp40, and inhibitorof caspase-activated DNase. J Biol Chem, 2002, 277:3364–3370.[11] Creagh EM, Sheehan D, Cotter TG: Heat shock proteinsmodulatorsof apoptosis in tumor cells. Leukemia, 2000;14: 1161–1173.[12] Mizushima Y, Wang P, Jarrar D: Preinduction of heat shockproteins protects cardiac and hepatic functions followingtrauma and hemorrhage. Am J Physiol Regul Integr CompPhysiol, 2000; 278: R352– R 359.[13] Sreedhar AS, Csemely P: Heat shock proteins in theregulation of apoptosis: new strategies in tumor therapy.A comprehensive review. Pharmac Therap, 2004; 10:227–257.[14] Sőti C, Csermely P: Aging cellular networks: Chaperonesas major participants. Exp Gerontol, 2007; 42:113–119.[15] Jolly C, Morimoto RI: Role of the heat shock responseand molecular chaperones in oncogenesis and cell death.J Natl Cancer Inst, 2000; 92: 1564–1572.[16] Powers MV, Workman P: Inhibitors of the heat shockresponse: Biology and Pharmacology. FEBS Lett, 2007,581: 3758–3769.[17] Ciechanover A: The ubiquitin proteolytic system andpathogenesis of human diseases: a novel platform formechanism-based drug targeting. Biochem Soc Trans,2003; 31: 474–481[18] Czarnecka A M, Campanella C, Zummo G, Cappello F:Heat shock protein 10 and signal transduction: a “capsulaeburnea” of carcinogenesis? Cell Stress Chaperones,2006; 11 (4): 287–294.[19] Adhikari AS, Sridhar Rao K, Rangaraj N, Parnaik VK,Mohan Rao C: Heat stress-induced localization of smallheat shock proteins in mouse myoblasts: intranuclearlamin A/C speckles as target for aBcrystallin and Hsp25.Exp Cell Res, 2004; 299: 393–403[20] Waters ER, Aevermann BD, Sanders-Reed Z: Comparativeanalysis of the small heat shock proteins in three angiospermgenomes identifies new subfamilies and revealsdiverse evolutionary patterns. Cell Stress Chaperones2008, 13 (2): 127–142.[21] Qiu XB, Shoa YM, Miao S, Wang L, The diversity of theDnaJ/Hsp40 family, the crucial partners for Hsp70 chaperones.Cell Mol Life Sci, 2006; Nov; 63 (22): 2560–2570.[22] Gupta RS: Evolution of the chaperonin families (Hsp60,Hsp10 and Tcp-1) of proteins and the origin of eukaryoticcells. Mol Microbiol, 1995; 15 (1): 1–11.[23] Hansen JJ, Bross P, Westergaard M, et al.: Genomicstructure of the human mitochondrial chaperonin genes:HSP60 and HSP10 are localised head to head on chromosome2 separated by a bidirectional promoter. Hu Gene,2003; 112 (1): 71–77.[24] Calabrese V, Mancuso C, Ravagna A, et al.: In vivo inductionof heat shock proteins in the substantia nigra followingL-DOPA administration is associated with increasedactivity of mitochondrial complex I and nitrosative stress inrats: regulation by glutathione redox state. J Neurochem,2007; 101 (3): 709–717.[25] Bukau B, Horwich AL: The Hsp 70 and Hsp 60 chaperonemachines. Cell, 1998; 92: 351–366.– 128 –