Reactivity of human preformed natural antibodies with various porcine pancreatic cells

2001 ◽  
Vol 21 (1) ◽  
pp. 59-61 ◽  
Author(s):  
Zhang Weijie ◽  
Xiong Pei ◽  
Liu Shaochun
1997 ◽  
Vol 29 (4) ◽  
pp. 2260-2261
Author(s):  
L. Inverardi ◽  
B. Clissi ◽  
F. Sanvito ◽  
C. Fazi ◽  
C. Ricordi ◽  
...  

1994 ◽  
Vol 26 (7) ◽  
pp. 553-562 ◽  
Author(s):  
Nicola Maggiano ◽  
Franco Citterio ◽  
Antonella Evangelista ◽  
Ubaldo Pozzetto ◽  
Marco Castagneto ◽  
...  

2001 ◽  
Vol 33 (7-8) ◽  
pp. 3865-3866
Author(s):  
W.J Zhang ◽  
P Xiong ◽  
S.C Liu ◽  
S.S Xia

1973 ◽  
Vol 5 (2) ◽  
pp. 162-166 ◽  
Author(s):  
C. Hammer ◽  
Ch. Chaussy ◽  
W. Brendel

Author(s):  
J. Metz ◽  
M. Merlo ◽  
W. G. Forssmann

Structure and function of intercellular junctions were studied under the electronmicroscope using conventional thin sectioning and freeze-etch replicas. Alterations of tight and gap junctions were analyzed 1. of exocrine pancreatic cells under cell isolation conditions and pancreatic duct ligation and 2. of hepatocytes during extrahepatic cholestasis.During the different steps of cell isolation of exocrine pancreatic cells, gradual changes of tight and gap junctions were observed. Tight junctions, which formed belt-like structures around the apex of control acinar cells in situ, subsequently diminished, became interrupted and were concentrated into macular areas (Fig. 1). Aggregations of membrane associated particles, which looked similar to gap junctions, were intermixed within tight junctional areas (Fig. 1). These structures continously disappeared in the last stages of the isolation procedure. The intercellular junctions were finally separated without destroying the integrity of the cell membrane, which was confirmed with porcion yellow, lanthanum chloride and horse radish peroxidase.


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