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2010 | 61 | 3 |

Tytuł artykułu

Survivin is a key factor in the differential susceptibility of gastric endothelial and epithelial cells to alcohol-induced injury

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
We previously demonstrated that the anti-apoptosis protein, survivin, plays a protective role against alcohol-induced gastric injury. Since the endothelium is a primary target of alcohol-induced gastric damage, we investigated whether survivin expression is a key factor in the greater susceptibility of gastric endothelial vs. epithelial cells to alcohol-induced injury. Here, we demonstrate that rat gastric epithelial cells (RGM1 cells, an epithelial cell line derived from normal rat gastric mucosa) expressed 7.5-fold greater survivin protein levels vs. rat gastric endothelial cells. Survivin expression correlated with resistance of gastric epithelial vs. endothelial cells to both alcohol-induced cell damage and alcohol-induced apoptosis. Suppression of survivin protein expression levels using siRNA rendered the gastric epithelial cells as susceptible to both alcohol-induced cell damage and apoptosis as the gastric endothelial cells. Conversely, forced overexpression of survivin by transient transfection rendered gastric endothelial cells as resistant to both alcohol-induced cell damage and apoptosis as mock-transfected gastric epithelial cells. Moreover, overexpression of a threonine-34 to glutamate phosphorylation mimic mutant survivin construct rendered gastric endothelial cells significantly more resistant to alcohol-induced damage and apoptosis vs. mock-transfected gastric epithelial cells. These findings indicate that disparate survivin expression levels can explain the discrepancy between gastric epithelial and endothelial cell susceptibility to alcohol-induced injury; and, that a negative charge at amino acid residue 34 on survivin, such as that which naturally occurs by phosphorylation of threonine-34, enhances its property in conferring gastric mucosal protection.

Wydawca

-

Rocznik

Tom

61

Numer

3

Opis fizyczny

p.253-264,fig.,ref.

Twórcy

autor
  • Research Healthcare Group, VA Long Beach Healthcare System, 5901 E. Seventh Street, Long Beach, CA 90822 USA
autor
autor

Bibliografia

  • Szabo S, Trier JS, Brown A, Schnoor J. Early vascular injury and increased vascular permeability in gastric mucosal injury caused by ethanol in the rat. Gastroenterology 1985; 88: 228-236.
  • Tarnawski A, Hollander D, Stachura J. Ultrastructural changes in the gastric mucosal microvessels after ethanol. Gastroenterol Clin Biol 1985; 9: 93-97.
  • Tarnawski A, Stachura J, Gergely H, Hollander D. Microvascular endothelium-a major target for alcohol injury of the human gastric mucosa. Histochemical and ultrastructural study. J Clin Gastroenterol 1988; 10(Suppl 1): S53-S64.
  • Mercer DW, Cross JM, Smith GS, Miller TA. Protective action of gastrin-17 against alcohol-induced gastric injury in the rat: role in mucosal defense. Am J Physiol Gastrointest Liver Physiol 1997; 273: G365-G373.
  • Tarnawski A, Hollander D, Stachura J, Krause WJ, Gergely H. Prostaglandin protection of the gastric mucosa against alcohol injury - a dynamic time-related process: the role of mucosal proliferative zone. Gastroenterology 1985; 88: 334-352.
  • Jones MK, Itani RM, Wang H, et al. Activation of VEGF and Ras genes in gastric mucosa during angiogenic response to ethanol injury. Am J Physiol Gastrointest Liver Physiol 1999; 276: G1345-G1355.
  • Chiou SK, Jones MK, Tarnawski AS. Survivin - an anti-apoptosis protein: its biological roles and implications for cancer and beyond. Med Sci Monit 2003; 9: P125-P129.
  • Wheatley SP, McNeish IA. Survivin: a protein with dual roles in mitosis and apoptosis. Int Rev Cytol 2005; 247: 35-88.
  • Lens SM, Vader G, Medema RH. The case for survivin as mitotic regulator. Curr Opin Cell Biol 2006; 18: 616-622.
  • Uren AG, Wong L, Pakusch M, et al. Survivin and the inner centromere protein INCENP show similar cell-cycle localization and gene knockout phenotype. Curr Biol 2000; 10: 1319-1328.
  • Fukuda S, Pelus LM. Regulation of the inhibitor-of-apoptosis family member survivin in normal cord blood and bone marrow CD34(+) cells by hematopoietic growth factors: implication of survivin expression in normal hematopoiesis. Blood 2001; 98: 2091-2100.
  • Gianani R, Jarboe E, Orlicky D, et al. Expression of survivin in normal, hyperplastic, and neoplastic colonic mucosa. Hum Pathol 2001; 32: 119-125.
  • Kobayashi Y, Yukiue H, Sasaki H, et al. Developmentally regulated expression of survivin in the human thymus. Hum Immunol 2002; 63: 101-107.
  • Chiou SK, Moon WS, Jones MK, Tarnawski AS. Survivin expression in the stomach: implications for mucosal integrity and protection. Biochem Biophys Res Commun 2003; 305: 374-379.
  • Jones MK, Padilla OR, Webb NA, Norng M. The anti-apoptosis protein, survivin, mediates gastric epithelial cell cytoprotection against ethanol-induced injury via activation of the p34cdc2 cyclin dependent kinase. J Cell Physiol 2008; 215: 750-764.
  • Livy DJ, Parnell SE, West JR. Blood ethanol concentration profiles: a comparison between rats and mice. Alcohol 2003; 29: 165-171.
  • Lee HB, Blaufox MD. Blood volume in the rat. J Nucl Med 1985; 26: 72-76.
  • Rattner DW, Ito S, Rutten MJ, Silen W. A rapid method for culturing guinea pig gastric mucous cell monolayers. in vitro Cell Dev Biol 1985; 21: 453-462.
  • Arakawa T, Nakamura A, Fukuda T, Higuchi K, Nakamura H, Kobayashi K. in vitro adaptive cytoprotection in gastric cells isolated from rat stomach. J Clin Gastroenterol 1990; 12(Suppl 1): S32-S38.
  • Gliddon BL, Nguyen NV, Gunn PA, Gleeson PA, van Driel IR. Isolation, culture and adenoviral transduction of parietal cells from mouse gastric mucosa. Biomed Mater 2008; 3(034117): 1-9.
  • Jones MK, Wang H, Tomikawa M, et al. Isolation and characterization of rat gastric microvascular cells as a model for studying gastric angiogenesis in vitro. J Physiol Pharmacol 2000; 51: 813-830.
  • Chiou SK, Tanigawa T, Akahoshi T, Abdelkari B, Jones MK, Tarnawski AS. Survivin: a novel target for indomethacin-induced gastric injury. Gastroenterology 2005; 128: 63-73.
  • Hawkey CJ, Kemp RT, Walt RP, Bhaskar NK, Davies J, Filipowicz B. Evidence that adaptive cytoprotection in rats is not mediated by prostaglandins. Gastroenterology 1988; 94: 948-954.
  • Balaa MA. Release of protective products, different from prostaglandins, by rat stomachs exposed to mild irritant. Dig Dis Sci 1989; 34: 429-435.
  • Schmidt KL, Smith GS, Miller TA. Microscopic correlates of adaptive cytoprotection in an ethanol injury model. Histol Histopathol 1989; 4: 105-115.
  • Mutoh H, Ota S, Hiraishi H, Ivey KJ, Terano A, Sugimoto T. Adaptive cytoprotection in cultured rat gastric mucus-producing cells. Role of mucus and prostaglandin synthesis. Dig Dis Sci 1995; 40: 872-878.
  • Ko JK, Cho CH. Adaptive gastric mucosal cytoprotection in rats: different models of action by three mild irritants. Digestion 1996; 57: 54-59.
  • Ko JK, Cho CH. Histological study of mechanisms of adaptive cytoprotection on ethanol-induced mucosal damage in rat stomachs. Dig Dis Sci 1998; 43: 1248-1257.
  • Kokoska ER, Smith GS, Rieckenberg CL, Deshpande Y, Banan A, Miller TA. Adaptive cytoprotection against deoxycholate-induced injury in human gastric cells in vitro: is there a role for endogenous prostaglandins? Dig Dis Sci 1998; 43: 806-815.
  • Kokoska ER, Smith GS, Wolff AB, et al. Role of calcium in adaptive cytoprotection and cell injury induced by deoxycholate in human gastric cells. Am J Physiol 1998; 275: G322-G330.
  • Rokutan K, Hirakawa T, Teshima S, et al. Implications of heat shock/stress proteins for medicine and disease. J Med Invest 1998; 44: 137-147.
  • Jones MK, Tomikawa M, Mohajer B, Tarnawski AS. Gastrointestinal mucosal regeneration: role of growth factors. Front Biosci 1999; 4: d303-d309.
  • Altieri DC. Molecular circuits of apoptosis regulation and cell division control: the survivin paradigm. J Cell Biochem 2004; 92: 656-663.
  • Pennati M, Folini M, Zaffaroni N. Targeting survivin in cancer therapy. Expert Opin Ther Targets 2008; 12: 463-476.
  • Knauer SK, Kramer OH, Knosel T, et al. Nuclear export is essential for the tumor-promoting activity of survivin. FASEB J 2007; 21: 207-216.
  • Connell CM, Colnaghi R, Wheatley SP. Nuclear survivin has reduced stability and is not cytoprotective. J Biol Chem 2008; 283: 3289-3296.
  • Barrett RM, Osborne TP, Wheatley SP. Phosphorylation of survivin at threonine 34 inhibits its mitotic function and enhances its cytoprotective activity. Cell Cycle 2009; 8: 278-283.
  • Gawad A, Ptak-Belowska A, Brzozowski T, Pawlik WW. Monocytes and vascular endothelial cells apoptosis. Role of p-HSP27. J Physiol Pharmacol 2009; 60: 55-61.
  • Pierzchalski P, Pytko-Polonczyk J, Jaworek J, Konturek SJ, Gonciarz M. Only live Helicobacter pylori is capable of caspase-3 dependent apoptosis induction in gastric mucosa epithelial cells. J Physiol Pharmacol 2009; 60: 119-128.
  • Zhang Y, Park TS, Gidday JM. Hypoxic preconditioning protects human brain endothelium from ischemic apoptosis by Akt-dependent survivin activation. Am J Physiol Heart Circ Physiol 2007; 292: H2573-H258.
  • Scalise A, Tucci MG, Lucarini G, et al. Local rh-VEGF administration enhances skin flap survival more than other types of rh-VEGF administration: a clinical, morphological and immunohistochemical study. Exp Dermatol 2004; 13: 682-690.
  • Fukuda S, Kaga S, Sasaki H, et al. Angiogenic signal triggered by ischemic stress induces myocardial repair in rat during chronic infarction. J Mol Cell Cardiol 2004; 36: 547-559.
  • Kaczmarek M, Frydrychowicz M, Nowicka A, et al. Influence of pleural macrophages on proliferative activity and apoptosis regulating proteins of malignant cells. J Physiol Pharmacol 2008; 59(Suppl 6): 321-330.
  • Conway EM, Pollefeyt S, Steiner-Mosonyi M, et al. Deficiency of survivin in transgenic mice exacerbates Fas-induced apoptosis via mitochondrial pathways. Gastroenterology 2002; 123: 619-631.
  • Deguchi M, Shiraki K, Inoue H, et al. Expression of survivin during liver regeneration. Biochem Biophys Res Commun 2002; 297: 59-64.
  • Tashiro M, Nakamura H, Taguchi M, Yoshikawa H, Otsuki M. Expression of survivin after acute necrohemorrhagic pancreatitis in rats. Pancreas 2003; 26: 160-165.

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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