Expression of the protooncogene jun is induced in the rat pancreas by cerulein infusion

Pancreas

Volumn 15, Issue 2, 1997, Pages 160-167

  Ferrara, Chiara ^a   Gress, Thomas M ^b   Mueller Pillasch, Friederike ^b   Lutz, Manfred P ^b   Weidenbach, Hans ^b   Poletti, Alessandro ^a   Lerch, Marcus M ^b   Del Favero, Giuseppe ^a   Adler, Guido ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b UNIVERSITY OF ULM   (Germany)

Author keywords

Acute pancreatitis; Cerulein; Protooncogene jun; Regeneration; Stimulation

Indexed keywords

CERULETIDE; CHOLECYSTOKININ; CHOLECYSTOKININ DERIVATIVE; CHOLECYSTOKININ RECEPTOR; ONCOPROTEIN;

ACINAR CELL; ACUTE PANCREATITIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA SYNTHESIS; MALE; NONHUMAN; ONCOGENE C FOS; ONCOGENE C JUN; ONCOGENE MYC; PRIORITY JOURNAL; RAT; TISSUE REGENERATION; TRANSCRIPTION INITIATION;

EID: 0030732767     PISSN: 08853177     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006676-199708000-00008     Document Type: Article

References (42)

1. Mutt V. Cholecystokinin: isolation, structure, and functions. In: Glass GBJ, ed. Gastrointestinal hormones. New York: Raven Press, 1980:169-221.
2. Solomon TE, Vanier M, Morisset J. Cell site and time course of DNA synthesis in pancreas after caerulein and secretin. Am J Physiol 1983;245:G99-105.
3. Lampel M, Kern HF. Acute interstitial pancreatitis in the rat induced by excessive doses of a pancreatic secretagogue. Virchows Arch [A] 1977;373:97-117.
4. Sankaran H, Goldfine CW, Bailey C, Licko V, Williams JA. Relationship of cholecystokinin receptor binding to regulation of biological functions in pancreatic acini. Am J Physiol 1982;242: G250-7.
5. Villaneuva ML, Martinez J, Bodanszky, Collins SM, Jensen RT, Gardner JD. Selective modification of the ability of cholecystokinin to cause residual stimulation of pancreatic enzyme secretion. Am J Physiol 1982;242:G416-22.
6. Saluja AK, Saluja M, Printz H, Zavertnik A, Sengupta A, Steer ML. Experimental pancreatitis is mediated by low-affinity cholecystokinin receptors that inhibit digestive enzyme secretion. Proc Natl Acad Sci USA 1989;86:8968-71.
7. Galas MC, Lignon MF, Rodriguez M, et al. Structure-activity relationship studies on cholecystokinin: analogues with partial agonist activity. Am J Physiol 1988;254:G176-82.
8. Stark HA, Sharp CM, Sutliff VE, Martinez J, Jensen RT. Gardner JD (1989). CCK-JMV-180: a peptide that distinguishes high-affinity cholecystokinin receptors from low-affinity cholecystokinin receptors. Biochim Biophys Acta 1989;1010:145-50.
9. Rivard N, Rydzewska G, Lods JS, Martinez J, Morisset J. Pancreas growth, tyrosine kinase, PtdIns 3-kinase, and PDL involve high-affinity CCK-receptor occupation. Am J Physiol 1994;266:G62-70.
10. Lutz MP, Sutor SL, Abraham RT, Miller LY. A role for cholecystokinin-stimulated protein tyrosine phosphorylation in regulated secretion by the pancreatic acinar cell. J Biol Chem 1993;268: 11119-24.
11. Lu L, Logsdon CD, CCK, bombesin, and carbachol stimulate c-fos, c-jun, and c-myc oncogene expression in rat pancreatic acini. Am J Physiol 1992;263:0327-32.
12. Angel P, Karin M. The role of jun, fos and the AP-1 complex in cell-proliferation and transformation. Biochim Biophys Acta 1991; 1072:129-57.
13. Vogt PK, Bos TJ. The oncogene jun and nuclear signalling. TIBS 1989;14:172-5.
14. Herschman HR. Primary response genes induced by growth factors and tumor promoters. Annu Rev Biochem 1991;60:281-319.
15. Ryseck RP, Hirai SI, Yaniv M, Bravo R. Transcriptional activation of c-jun during the G0/G1 transition in mouse fibroblasts. Nature 1988;334:535-7.
16. Lamph WW, Wamsley P, Sassoni-Corsi P, Verma IM. Induction of proto-oncogene jun/AP-1 by serum and TPA. Nature 1988;334: 629-31.
17. Angel P, Baumann I, Stein B, Delius H, Rahmsdorf HJ, Herrlich P. 12-O-Tetradecanoyl-phorbol-13-acetate induction of the human collagenase gene is mediated by an inducible enhancer element located in the 5′-flanking region. Mol Cell Biol 1987;7:2256-66.
18. Schoenthal A, Herrlich P, Rahmsdorf HJ, Ponta H. Requirement for fos gene expression in the transcriptional activation of collagenase by other oncogenes and phorbol esters. Cell 1988;54:325-34.
19. Kerr LD, Miller DB, Martrisia LM, TGF beta-1 inhibition of transin/stromelysin gene expression is mediated through a Fos binding sequence. Cell 1990;61:267-78.
20. Lee W, Mitchell P, Tjian R. Purified transcription factor AP-1 interacts with TPA-inducible enhancer elements. Cell 1987;49: 741-52.
21. Jonat C, Rahmsdorf HJ, Park K-K, et al. Antitumor promotion and antiinflammation: down-modulation of AP-1 (fos/jun) activity by glucocorticoid hormone. Cell 1990;62:1189-204.
22. Glaub MP, Bellard M, Scheuer I, Chambon P, Sassoni-Corsi P. Activation of the ovoalbumin gene by the estrogen receptor involves the fos/jun complex. Cell 1990;63:1267-76.
23. Shuele R, Umesono K, Mangelsdorf DJ, Balado J, Pike JW, Evans RM. Jun-fos and receptors for vitamins A and D recognize a common response element in the human osteocalcin gene. Cell 1990; 61:497-504.
24. Persson H, Leder P. Nuclear localization and DNA binding properties of a protein expressed by the human c-myc oncogene. Science 1984;225:718-21.
25. Blackwell TK, Kretzner L, Blackwood EM, Eisenman RN, Weintraub H. Sequence-specific DNA binding by the c-myc protein. Science 1990;250:1149-52.
26. Ryder K, Nathans D. Induction of protooncogene c-jun by serum growth factors. Proc Natl Acad Sci USA 1988;85:8464-7.
27. Alitalo K, Bishop JM, Smith DH, Chen EY, Colby WW, Levinson AD. Nucleotide sequence to the v-myc oncogene of avian retrovirus MC29. Proc Natl Acad Sci USA 1983:801(1):100-4.
28. Curran T, MacConnell WP, Van Straaten F, Verma IM. Structure of the FBJ murine osteosarcoma virus genome: molecular cloning of its associated helper virus and the cellular homolog of the v-fos gene from mouse and human cells. Mol Cell Biol 1983;3(5):914-21.
29. Sambrook J, Fritsch EF, Maniatis T. Molecular cloning: a laboratory manual. Cold Spring Harbor, NY: Cold Spring Harbor Press, 1989.
30. Gress T, Hoheisel JD, Lennon GG, Zehetner G, Lehrach H. Hybridisation fingerprinting of high-density cDNA library arrays with cDNA pools derived from whole tissues. Mammal Genome 1992; 3:609-19.
31. Gress T, Mueller-Pillasch F, Elsaesser HP, et al. Enhancement of transforming growth factor β1 expression in the rat pancreas during regeneration from caerulein-induced pancreatitis. Eur J Clin Invest 1994;24:679-85.
32. Wicker C, Puigserver A, Rausch C, Scheele G, Kern H. Multiple-level caerulein control of the gene expression of secretory proteins in the rat pancreas. Eur J Biochem 1985;151:461-6.
33. Steinhilber W, Poensgen J, Rausch U, Kern HF, Scheele GA. Translational control of anionic trypsinogen and amylase synthesis in rat pancreas in response to caerulein stimulation. Proc Natl Acad Sci USA 1988;85:6597-601.
34. 2+ mobilization and phospholipid hydrolysis in isolated rat pancreatic acini. Studies using a new cholecystokinin analog, JMV-180. J Biol Chem 1990;265:6247-54.
35. Saluja AK, Dawra RK, Lerch MM, Steer ML, CCK-JMV-180, an analog of cholecystokinin, releases intracellular calcium from an inositol triphosphate-independent pool in rat pancreatic acini. J Biol Chem 1992;267:11202-7.
36. Adler G, Hupp T, Kern HF. Course and spontaneous regression of acute pancreatitis in the rat pancreas. Virchows Arch [A] 1979;382: 31-7.
37. Elsaesser HP, Adler G, Kern HF. Time course and cellular source of pancreatic regeneration following acute pancreatitis in the rat. Pancreas 1986;1:421-9.
38. Cowley BD, Chadwick LJ Jr, Grantham JJ, Calvet JP. Sequential protooncogene expression in regenerating kidney following acute renal injury. J Biol Chem 1989;264(14):8389-93.
39. Thompson NL, Mead JE, Braun L, Goyette M, Shank PR, Fausto N, Sequential protooncogene expression during rat liver regeneration. Cancer Res 1986;46:3111-7.
40. Kurokawa N, Hirotani Y, Arakwa Y, et al. Increased production of c-myc and c-fos-related proteins during late stage of regenerative process in rat liver after partial hepatectomy. Biomed Res 1990;11 (3):165-72.
41. Calvo EL, Dusetti NJ, Cadenas MB, Dagorn JC, Iovanna JL. Changes in gene expression during pancreatic regeneration: activation of c-myc and H-ras oncogenes in the rat pancreas. Pancreas 1991;6(2):150-6.
42. Luetcke H, Scheele GA, Kern HF. Time course and cellular site of mitotic activity in the exocrine pancreas of the rat during sustained hormone stimulation. Cell Tissue Res 1987;247:385-91.