XIA Ming, PAN Xue, LI Min-Yan, DENG Min, ZHANG Yong, JI Yi, CHEN Yi, WANG He-Sheng, KONG De-Ming. ANALYSES OF β-CELL DEVELOPMENT IN TRANSGENIC ZEBRAFISHW ITH A CONSTRUCT OF INSULIN PROMOTER AND GREEN FLUORESCENT PROTEIN[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(4): 702-708.
Citation: XIA Ming, PAN Xue, LI Min-Yan, DENG Min, ZHANG Yong, JI Yi, CHEN Yi, WANG He-Sheng, KONG De-Ming. ANALYSES OF β-CELL DEVELOPMENT IN TRANSGENIC ZEBRAFISHW ITH A CONSTRUCT OF INSULIN PROMOTER AND GREEN FLUORESCENT PROTEIN[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(4): 702-708.

ANALYSES OF β-CELL DEVELOPMENT IN TRANSGENIC ZEBRAFISHW ITH A CONSTRUCT OF INSULIN PROMOTER AND GREEN FLUORESCENT PROTEIN

Funds: 

Founds of province(No.2006109)

  • Received Date: January 20, 2008
  • Rev Recd Date: April 11, 2009
  • Published Date: July 24, 2009
  • W ith many advantageous features such as small size, high production and fertilization in vitro, zebrafish has become a kind of themodel creature for the investigation of vertebrate development and human diseases. Sowe set up a transgenic zebrafish model to investigate the β-cell development1 Firstly, we obtained an INS: GFP construction that contains the zebrafish insulin (INS) promoter and green fluorescent protein (GFP).Secondly, we injected the construction into the cytoplasm of one-cell-stage embryos. F inally, we gained germline INS transgenic zebrafish that d isplayed highly specific β-cell expression ofGFP in both larvae and adult1 By following GFP expression, pancreas formation was detected at the 18h post-fertilization in the earliest time points between the second bilateral som ites, a group of GFP-positive cells located from ventral to the notochord. From day 1 to 5 post-fertilization,the number of insu lin/GFP expressing cells migrated and formed a right organ. Thus, ourworks demonstrated that the transgenic line provided a conven ient and d irect expermi ental tool in analyzing endocrine pancreas development, injury and recovery.
  • [1]
    Shapiro A M, L akey JR, Ryan E A, et al. Islet transplantation in seven patientsw ith type. diabetesmellitus using a glucocort-icoid-free immunosuppressive regimen [J]. N EnglJ M ed, 2000, 343: 230-238
    [2]
    DorY, Brown J, M artinezO I, et al. Adult pancreatic beta-cells are formed by sel-f duplication rather than stem-cell differentiation[J]. N ature, 2004, 429: 41-46
    [3]
    Porat S, DorY. N ew sources of pancreatic beta cells [J]. Curr D iab Rep, 2007, 7: 304-308
    [4]
    Huang H, VogelS S, Liu N, et al. Analysis ofpancreatic development in living transgenic zebrafish embryos [J]. Mol Cell Endocrinol, 2001, 177: 117-124
    [5]
    Rembo ldM, LahiriK, FoulkesN S, et al. Transgenesis in fish: efficient selection of transgenic fish by co-injection w ith a fluorescent reporter construct [J]. N at Protoc, 2006, 1: 1133-1139
    [6]
    K inoshitaM, Kani S, O zato K, et al. Activity of themedaka translation elongation factor 1alpha-A promoter examined using the GFP gene as a reporter [J]. Dev Growth D iffer, 2000, 42: 469-478
    [7]
    W esterfield M1 The Zebrafish Book [M]. Institute of N euroscienceU niversity of Oregon. 1995, 16-21
    [8]
    W anH, Korzh S, Li Z, et al. Analyses of pancreas development by generation of gfp transgenic zebrafish using an exocrine pancreas-specific elastaseA gene promoter [J]. Exp CellRes, 2006 312: 1526-1539
    [9]
    Szkudelski T. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas [J]. Physiol Res, 2001, 50:537-546
    [10]
    Biemar F, Argenton F, Schm idtke R, et al. Pancreas development in zebrafish: early dispersed appearance of endocrine hormone expressing cells and their convergence to form the definitive islet [J]. Dev Biol, 2001, 230: 189-203
    [11]
    Yee N S, Yusuff S, PackM. Zebrafish pdx. morphant displays defects in pancreas development and digestive organ chirality, and potentially identifies a multipotent pancreas progenitor cell [J]. Genesis, 2001, 30: 137-140
    [12]
    K im H J, Sumanas S, Palencia-Desai S, et al. G enetic analysis of early endocrine pancreas formation in zebrafish [J]. Mol Endocrinol,2006, 20: 194-203
    [13]
    W ardA B, W arga R M, P rince V E. O rigin of the zebrafish endocrine and exocrine pancreas [J]. D ev Dyn,2007, 236: 1558-1569
    [14]
    SpederP, Petzo ldt A, Suzanne M, et al. Strateg ies to establish left/right asymmetry in vertebrates and invertebrates [J]. Curr Opin GenetD ev, 2007, 17: 351-358
    [15]
    Aylsworth A S. C linical aspects of defects in the determ ination of laterality [J]. Am J M ed Genet, 2001, 101:345-355
    [16]
    P isharath H. Validation of nitroreductase, a prodrug-activating enzyme, mediated cell death in embryonic zebrafish (Danio rerio) [J]. Comp M ed, 2007, 57: 241-246
    [17]
    P isharath H, Rhee JM, SwansonM A, et al. T argeted ablation of beta cells in the embryonic zebrafish pancreas using E. colin-itroreductase [J]. M ech Dev, 2007, 124: 218-229
    [18]
    Curado S, Anderson R M, Jungblut B, et al. Conditional targeted cell ablation in zebrafish: a new too l for regeneration studies [J]. D ev Dyn, 2007, 236: 1025-1035
    [19]
    M cGonnell IM, Fowkes R C. F ishing for gene function-endocrine modelling in the zebrafish [J]. J Endocrinol, 2006, 189:425-439

Catalog

    Article views (884) PDF downloads (432) Cited by()
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return