Assessment of human pancreatic islet architecture and composition by laser scanning confocal microscopy

被引:565
作者
Brissova, M
Fowler, MJ
Nicholson, WE
Chu, A
Hirshberg, B
Harlan, DM
Powers, AC
机构
[1] Vanderbilt Univ, Div Diabet Endocrinol & Metab, Sch Med, Nashville, TN 37232 USA
[2] NIDDKD, Islet & Autoimmun Branch, Bethesda, MD 20892 USA
[3] VA Tennessee Valley Healthcare Syst, Nashville, TN USA
关键词
pancreatic islets; confocal microscopy; architecture; composition;
D O I
10.1369/jhc.5C6684.2005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The recent success of pancreatic islet transplantation has generated considerable enthusiasm. To better understand the quality and characteristics of human islets used for transplantation, we performed detailed analysis of islet architecture and composition using confocal laser scanning microscopy. Human islets from six separate isolations provided by three different islet isolation centers were compared with isolated mouse and non-human primate islets. As expected from histological sections of murine pancreas, in isolated murine islets a and 6 cells resided at the periphery of the p-cell core. However, human islets were markedly different in that alpha, beta, and delta cells were dispersed throughout the islet. This pattern of cell distribution was present in all human islet preparations and islets of various sizes and was also seen in histological sections of human pancreas. The architecture of isolated non-human primate islets was very similar to that of human islets. Using an image analysis program, we calculated the volume of (alpha, beta, and delta cells. In contrast to murine islets, we found that populations of islet cell types varied considerably in human islets. The results indicate that human islets not only are quite heterogeneous in terms of cell composition but also have a substantially different architecture from widely studied murine islets.
引用
收藏
页码:1087 / 1097
页数:11
相关论文
共 28 条
  • [1] BEATENS D, 1979, SCIENCE, V206, P1323
  • [2] Bennett BD, 1996, J BIOL CHEM, V271, P3647
  • [3] Biancone L, 2002, CELL TRANSPLANT, V11, P309
  • [4] 3-DIMENSIONAL IMAGING OF INTACT ISOLATED ISLETS OF LANGERHANS WITH CONFOCAL MICROSCOPY
    BRELJE, TC
    SCHARP, DW
    SORENSON, RL
    [J]. DIABETES, 1989, 38 (06) : 808 - 814
  • [5] Reduction in pancreatic transcription factor PDX-1 impairs glucose-stimulated insulin secretion
    Brissova, M
    Shiota, M
    Nicholson, WE
    Gannon, M
    Knobel, SM
    Piston, DW
    Wright, CVE
    Powers, AC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) : 11225 - 11232
  • [6] β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes
    Butler, AE
    Janson, J
    Bonner-Weir, S
    Ritzel, R
    Rizza, RA
    Butler, PC
    [J]. DIABETES, 2003, 52 (01) : 102 - 110
  • [7] CIRULLI V, 1994, J CELL SCI, V107, P1429
  • [8] Dahl U, 1996, DEVELOPMENT, V122, P2895
  • [9] Expression of peroxisome proliferator-activated receptor γ (PPARγ) in normal human pancreatic islet cells
    Dubois, M
    Pattou, F
    Kerr-Conte, J
    Gmyr, V
    Vandewalle, B
    Desreumaux, P
    Auwerx, J
    Schoonjans, K
    Lefebvre, J
    [J]. DIABETOLOGIA, 2000, 43 (09) : 1165 - 1169
  • [10] Neural cell adhesion molecule (N-CAM) is required for cell type segregation and normal ultrastructure in pancreatic islets
    Esni, F
    Täljedal, IB
    Perl, AK
    Cremer, H
    Christofori, G
    Semb, H
    [J]. JOURNAL OF CELL BIOLOGY, 1999, 144 (02) : 325 - 337