Comparative Analysis of Phospholipase D2 Localization in the Pancreatic Islet of Rat and Guinea Pig

  • Ryu, Gyeong-Ryul (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Kim, Myung-Jun (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Song, Chan-Hee (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Min, Do-Sik (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Rhie, Duck-Joo (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Yoon, Shin-Hee (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Hahn, Sang-June (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Kim, Myung-Suk (Deportment of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Jo, Yang-Hyeok (Deportment of Physiology, College of Medicine, The Catholic University of Korea)
  • Published : 2003.08.21

Abstract

To examine the localization pattern of phospholipase D2 (PLD2) in the pancreatic islet (the islet of Langerhans) depending on species, we conducted a morphological experiment in the rat and guinea pig. Since individual islets display a typical topography with a central core of B cell mass and a peripheral boundary of A, D, and PP cells, double immunofluorescent staining with a panel of antibodies was performed to identify PLD2-immunoreactive cells in the islets PLD2 immunoreactivity was mainly present in A and PP cells of the rat pancreatic islets. And yet, in the guinea pig, PLD2 immunoreactivity was exclusively localized in A cells, and not in PP cells. These findings suggest a possibility that PLD2 is mainly located in A cells of rodent pancreatic islets, and that the existence of PLD2 in PP cells is not universal in all species. Based on these results, it is suggested that PLD2 may play a significant role in the function of A and/or PP cells via a PLD-mediated signaling pathway.

Keywords

References

  1. Boarder MR. A role of phospholipase D in control of mitogenesis. Trends Pharmacol Sci 15: 57-62, 1994 https://doi.org/10.1016/0165-6147(94)90111-2
  2. Chen M-C, Paez-Espinosa V, Welsh N, Eizirik DL. Interleukin-1 $\beta$ regulates phospholipase D-1 expression in rat pancreatic $\beta$-cells. Endocrinology 141: 2822-2828, 2000 https://doi.org/10.1210/en.141.8.2822
  3. Cockcroft S. ARF-regulated phospholipase D: a potential role in membrane traffic. Chem Phys Lipids 80: 59-80, 1996 https://doi.org/10.1016/0009-3084(96)02546-7
  4. Colley WC, Sung TC, Roll R, Jenco J, Hammond SM, Altshuller Y, Bar-Sagi D, Morris AJ, Frohman MA. Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization. Curr Biol 7: 191-201, 1997 https://doi.org/10.1016/S0960-9822(97)70090-3
  5. Deeg MA, Verchere B. Regulation of glycosylphosphatidylinositolspecific phospholipase D secretion from $\beta$TC3 cells. Endocrinology 138: 819-826, 1997 https://doi.org/10.1210/en.138.2.819
  6. Dunlop M, Metz SA. Activation of phospholipase D by glyceraldehydes in isolated islet cells follows protein kinase C activation. Endocrinology 130: 93-101, 1992 https://doi.org/10.1210/en.130.1.93
  7. Exton JH. Phosphatidylcholine breakdown and signal transduction. Biochim Biophys Acta 1212: 26-42, 1994 https://doi.org/10.1016/0005-2760(94)90186-4
  8. Exton JH. Phospholipase D: enzymology, mechanisms of regulation, and function. Physiol Rev 77: 303-320, 1997 https://doi.org/10.1152/physrev.1997.77.2.303
  9. Hammond SM, Jenco JM, Nakashima S, Cadwallader K, Gu Q, Cook S, Nozawa Y, Prestwich GD, Frohman MA, Morris AJ. Characterization of two alternately spliced forms of phospholipase D1. J Biol Chem 272: 3860-3868, 1997 https://doi.org/10.1074/jbc.272.6.3860
  10. Hsu S, Raine L, Fanger H. The use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabelled antibody (PAP) procedures. J Histochem Cytochem 29: 577-580, 1981 https://doi.org/10.1177/29.4.6166661
  11. Kodaki T, Yamashita S. Cloning, expression, and characterization of a novel phospholipase D complementary DNA from rat brain. J Biol Chem 272: 11408-11413, 1997 https://doi.org/10.1074/jbc.272.17.11408
  12. Laine J, Bourgoin S, Bourassa J, Morisset J. Subcellular distribution and characterization of rat pancreatic phospholipase D isoforms. Pancreas 20: 323-326, 2000 https://doi.org/10.1097/00006676-200005000-00001
  13. Lee MY, Kim SY, Min DS, Choi YS, Shin SL, Chun MH, Lee SB, Kim M-S, Jo Y-H. Upregulation of phospholipase D in astrocytes in response to transient forebrain ischemia. Glia 30: 311-317, 2000 https://doi.org/10.1002/(SICI)1098-1136(200005)30:3<311::AID-GLIA10>3.0.CO;2-K
  14. Metz SA, Dunlop M. Stimulation of insulin release by phospholipase D. Biochem J 270: 427-435, 1990 https://doi.org/10.1042/bj2700427
  15. Metz CN, Zhang Y, Guo Y, Tsang TC, Kochan JP, Altszuler N, Davitz MA. Production of the glycosylphosphatidylinositol-specific phospholipase D by the islets of Langerhans. J Biol Chem 266: 17733-17736, 1991
  16. Min B-H, Jeong S-Y, Kang S-W, Crabo BG, Foster DN, Chun B-G, Bendayan M, Park I-S. Transient expression of clusterin (sulfated glycoprotein-2) during development of rat pancreas. J Endocrinol 158: 43-52, 1998a https://doi.org/10.1677/joe.0.1580043
  17. Min DS, Park SK, Exton JH. Characterization of a rat brain phospholipase D isozyme. J Biol Chem 272: 7044-7051, 1998b
  18. Min DS, Shin KS, Kim E-G, Kim SR, Yoon SH, Kim M-S, Jo Y-H. Down-regulation of phospholipase D during differentiation of mouse F9 teratocarcinoma cells. FEBS Lett 454: 197-200, 1999 https://doi.org/10.1016/S0014-5793(99)00798-X
  19. Min DS, Cho NJ, Yoon S-H, Lee YH, Hahn SJ, Lee KH, Kim M-S, Jo Y-H. Phsopholipase C, protein kinase C, Ca2+/calmodulindependent protein kinase II, and tyrosine phosphorylation are involved in carbachol-induced phospholipase D activation in Chinese hamster ovary cells expressing muscarinic acetylcholine receptor of Caenorhabditis elegans. J Neurochem 75: 274-281, 2000 https://doi.org/10.1046/j.1471-4159.2000.0750274.x
  20. Orci L, Unger R. Functional subdivision of islets of Langerhans and possible role of D-cells. Lancet 2: 1243-1244, 1975
  21. Roth MG, Sternweis PC. The role of lipid signaling in constitutive membrane traffic. Curr Opin Cell Biol 9: 519-526, 1997 https://doi.org/10.1016/S0955-0674(97)80028-2
  22. Ryu GR, Kim M-J, Song C-H, Sim SS, Min DS, Rhie D-J, Yoon SH, Hahn SJ, Kim M-S, Jo Y-H. Site-specific distribution of phospholipase D isoforms in the rat pancreas. Acta Histochem Cytochem 36: 51-60, 2003 https://doi.org/10.1267/ahc.36.51
  23. Yibchok-anun, S, Cheng, H, Abu-Basha, E. A, Ding, J, Ioudina, M. and Hsu, W. H. Mechanisms of bradykinin-induced glucagon release in clonal $\alpha$-cells In-R1-G9: involvement of Ca2$^+$-dependent and independent pathways. Mol Cell Endocrinol 192; 27- 36, 2002 https://doi.org/10.1016/S0303-7207(02)00115-6
  24. Zheng L, Krsmanovic LZ, Vergara LA, Catt KJ, Stojilkovic SS. Dependence of intracellular signaling and neurosecretion on phospholipase D activation in immortalized gonadotropin-releasing hormone neurons. Proc Natl Acad Sci USA 94: 1573-1578, 1997 https://doi.org/10.1073/pnas.94.4.1573