Unfolding protein response signaling is involved in development, maintenance, and regression of the corpus luteum during the bovine estrous cycle

Biochemical and Biophysical Research Communications

Volumn 441, Issue 2, 2013, Pages 344-350

  Park, Hyo Jin ^a   Park, Sun Ji ^a   Koo, Deog Bon ^b   Kong, Il Keun ^c   Kim, Min Kyu ^d   Kim, Jin Man ^d   Choi, Myung Sook ^a   Park, Young Ho ^e   Kim, Sun Uk ^e   Chang, Kyu Tae ^e   Park, Choon Keun ^f   Chae, Jung Il ^g   Lee, Dong Seok ^a  

^a Kyungpook National University   (South Korea)

^b Daegu University   (South Korea)

^c Gyeongsang National University   (South Korea)

^d Chungnam National University   (South Korea)

^e Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

^f Kangwon National University   (South Korea)

^g Chonbuk National University   (South Korea)

Author keywords

Corpus luteum; ER stress; Estrous cycle; Progesterone; Steroidogenic enzymes; Unfolding protein response

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 4; CASPASE 3; GLUCOSE REGULATED PROTEIN 78; GROWTH ARREST AND DNA DAMAGE INDUCIBLE PROTEIN 153; INITIATION FACTOR 2ALPHA; MESSENGER RNA; PROTEIN GADD34; PROTEIN IRE1; PROTEIN P50ATF6; PROTEIN P90ATF6; STRESS ACTIVATED PROTEIN KINASE; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; X BOX BINDING PROTEIN 1;

ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELLULAR STRESS RESPONSE; CONTROLLED STUDY; CORPUS LUTEUM; COW; DEVELOPMENTAL STAGE; ENDOPLASMIC RETICULUM STRESS; ESTRUS CYCLE; FEMALE; GENE EXPRESSION; LIFESPAN; NONHUMAN; PRIORITY JOURNAL; PROTEIN CLEAVAGE; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; UNFOLDED PROTEIN RESPONSE;

CORPUS LUTEUM; ER STRESS; ESTROUS CYCLE; PROGESTERONE; STEROIDOGENIC ENZYMES; UNFOLDING PROTEIN RESPONSE;

3-HYDROXYSTEROID DEHYDROGENASES; ACTIVATING TRANSCRIPTION FACTOR 6; ANIMALS; CATTLE; CORPUS LUTEUM; DNA-BINDING PROTEINS; ENDOPLASMIC RETICULUM-ASSOCIATED DEGRADATION; ESTROUS CYCLE; FEMALE; GENE EXPRESSION REGULATION, ENZYMOLOGIC; HEAT-SHOCK PROTEINS; LUTEOLYSIS; PROTEIN UNFOLDING; SIGNAL TRANSDUCTION; TRANSCRIPTION FACTORS; UNFOLDED PROTEIN RESPONSE;

BOVINAE;

EID: 84888004144     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2013.10.056     Document Type: Article

References (29)

1. K. Okuda, and R. Sakumoto Multiple roles of TNF super family members in corpus luteum function Reprod. Biol. Endocrinol. 1 2003 95
2. S. Jiemtaweeboon, K. Shirasuna, A. Nitta, A. Kobayashi, H.J. Schuberth, T. Shimizu, and A. Miyamoto Evidence that polymorphonuclear neutrophils infiltrate into the developing corpus luteum and promote angiogenesis with interleukin-8 in the cow Reprod. Biol. Endocrinol. 9 2011 79
3. J.S. Richards, D.L. Russell, R.L. Robker, M. Dajee, and T.N. Alliston Molecular mechanisms of ovulation and luteinization Mol. Cell. Endocrinol. 145 1998 47 54
4. R. Rekawiecki, M.K. Kowalik, D. Slonina, and J. Kotwica Regulation of progesterone synthesis and action in bovine corpus luteum J. Physiol. Pharmacol. 59 Suppl. 9 2008 75 89
5. S. Oyadomari, and M. Mori Roles of CHOP/GADD153 in endoplasmic reticulum stress Cell Death Differ. 11 2004 381 389
6. E.D. Lai, T. Teodoro, and A. Volchuk Endoplasmic reticulum stress: signaling the unfolded protein response Physiology 22 2007 193 201
7. M. Ito, H. Nakagawa, T. Okada, S. Miyazaki, and S. Matsuo ER-stress caused by accumulated intracistanal granules activates autophagy through a different signal pathway from unfolded protein response in exocrine pancreas cells of rats exposed to fluoride Arch. Toxicol. 83 2009 151 159
8. R. Jager, M.J. Bertrand, A.M. Gorman, P. Vandenabeele, and A. Samali The unfolded protein response at the crossroads of cellular life and death during endoplasmic reticulum stress Biol. Cell 104 2012 259 270
9. P. Walter, and D. Ron The unfolded protein response: from stress pathway to homeostatic regulation Science 334 2011 1081 1086
10. I. Kim, W. Xu, and J.C. Reed Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities Nat. Rev. Drug Discovery 7 2008 1013 1030
11. E. Szegezdi, S.E. Logue, A.M. Gorman, and A. Samali Mediators of endoplasmic reticulum stress-induced apoptosis EMBO Rep. 7 2006 880 885
12. S.J. Park, T.S. Kim, C.K. Park, S.H. Lee, J.M. Kim, K.S. Lee, I.K. Lee, J.W. Park, M.A. Lawson, and D.S. Lee HCG-induced endoplasmic reticulum stress triggers apoptosis and reduces steroidogenic enzyme expression through activating transcription factor 6 in Leydig cells of the testis J. Mol. Endocrinol. 50 2013 151 166
13. Y. Miyamoto, D.J. Skarzynski, and K. Okuda Is tumor necrosis factor alpha a trigger for the initiation of endometrial prostaglandin F-2 alpha release at luteolysis in cattle? Biol. Reprod. 62 2000 1109 1115
14. J.A. Arosh, J. Parent, P. Chapdelaine, J. Sirois, and M.A. Fortier Expression of cyclooxygenases 1 and 2 and prostaglandin E synthase in bovine endometrial tissue during the estrous cycle Biol. Reprod. 67 2002 161 169
15. G.I. Nepomniashchikh, S.V. Aidagulova, and L.M. Nepomniashchikh Morphological characteristics of the stomach of microtinae rodents from ecologically dangerous regions Biull. Eksp. Biol. Med. 121 1996 711 715
16. S. Verma-Kumar, S.V. Srinivas, P. Muraly, V.K. Yadav, and R. Medhamurthy Cloning of a buffalo (Bubalus bubalis) prostaglandin F(2alpha) receptor: changes in its expression and concentration in the buffalo cow corpus luteum Reproduction 127 2004 705 715
17. C. Stocco, C. Telleria, and G. Gibori The molecular control of corpus luteum formation, function, and regression Endocr. Rev. 28 2007 117 149
18. D.A. Redmer, V. Doraiswamy, B.J. Bortnem, K. Fisher, A. Jablonka-Shariff, A.T. Grazul-Bilska, and L.P. Reynolds Evidence for a role of capillary pericytes in vascular growth of the developing ovine corpus luteum Biol. Reprod. 65 2001 879 889
19. J. Wu, and R.J. Kaufman From acute ER stress to physiological roles of the unfolded protein response Cell Death Differ. 13 2006 374 384
20. S. Luo, C. Mao, B. Lee, and A.S. Lee GRP78/BiP is required for cell proliferation and protecting the inner cell mass from apoptosis during early mouse embryonic development Mol. Cell. Biol. 26 2006 5688 5697
21. S. Franceschelli, O. Moltedo, G. Amodio, G. Tajana, and P. Remondelli In the Huh7 hepatoma cells diclofenac and indomethacin activate differently the unfolded protein response and induce er stress apoptosis Open Biochem. J. 5 2011 45 51
22. M. Wang, S. Wey, Y. Zhang, R. Ye, and A.S. Lee Role of the unfolded protein response regulator GRP78/BiP in development, cancer, and neurological disorders Antioxid. Redox Signal. 11 2009 2307 2316
23. E. Kojima, A. Takeuchi, M. Haneda, F. Yagi, T. Hasegawa, K. Yamaki, K. Takeda, S. Akira, K. Shimokata, and K. Isobe The function of GADD34 is a recovery from a shutoff of protein synthesis induced by ER stress - elucidation by GADD34-deficient mice FASEB J. 17 2003 1573 1575
24. N. Badiola, C. Penas, A. Minano-Molina, B. Barneda-Zahonero, R. Fado, G. Sanchez-Opazo, J.X. Comella, J. Sabria, C. Zhu, K. Blomgren, C. Casas, and J. Rodriguez-Alvarez Induction of ER stress in response to oxygen-glucose deprivation of cortical cultures involves the activation of the PERK and IRE-1 pathways and of caspase-12 Cell Death Dis. 2 2011 e149
25. K. Haze, H. Yoshida, H. Yanagi, T. Yura, and K. Mori Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress Mol. Biol. Cell 10 1999 3787 3799
26. M. Myers, S. van den Driesche, A.S. McNeilly, and W.C. Duncan Activin A reduces luteinisation of human luteinised granulosa cells and has opposing effects to human chorionic gonadotropin in vitro J. Endocrinol. 199 2008 201 212
27. E. Szegezdi, S.E. Logue, A.M. Gorman, and A. Samali Mediators of endoplasmic reticulum stress-induced apoptosis EMBO Rep. 7 2006 880 885
28. K.L. Lin, C.C. Huang, J.S. Cheng, J.Y. Tsai, Y.C. Lu, H.T. Chang, and C.R. Jan Ketoconazole-induced JNK phosphorylation and subsequent cell death via apoptosis in human osteosarcoma cells Toxicol. In Vitro 23 2009 1268 1276
29. G. Jing, J.J. Wang, and S.X. Zhang ER stress and apoptosis: a new mechanism for retinal cell death Exp. Diabetes Res. 2012 2012 589589