In situ islet cytokine gene expression during development of type I diabetes in the non-obese diabetic mouse

1994 ◽  
Vol 39 (3) ◽  
pp. 283-288 ◽  
Author(s):  
H. Toyoda ◽  
B. Formby ◽  
D. Magalong ◽  
A. Redford ◽  
E. Chan ◽  
...  
2005 ◽  
Vol 42 (5) ◽  
pp. 579-588 ◽  
Author(s):  
S. Tanaka ◽  
M. Sato ◽  
T. Onitsuka ◽  
H. Kamata ◽  
Y. Yokomizo

The granulomatous lesions in bovine paratuberculosis have been classified into two types, i.e., the lepromatous type and the tuberculoid type. To clarify the immunopathologic mechanisms at the site of infection, we compared inflammatory cytokine gene expression between the two types of lesions. Samples were obtained from noninfected control cows ( n =5) and naturally infected cows ( n =7) that were diagnosed by enzyme-linked immunosorbent assay (ELISA) and fecal culture test. Although none of the infected cows showed clinical signs, tuberculoid lesions were observed in five cows (tuberculoid group) and lepromatous lesions in two cows (lepromatous group). Among the cytokines examined by reverse transcription-polymerase chain reaction (RT-PCR), Th2-type cytokines interleukin-4 (IL-4) and IL-10, and Th1-type cytokine IL-2 were expressed more significantly in the lepromatous group than in the tuberculoid ( P < 0.01) and noninfected groups ( P < 0.05). No statistical differences were observed in the expression of interferon-gamma, IL-1 beta, TNF-alpha, and GM-CSF among lepromatous, tuberculoid, and noninfected groups. Expression of proinflammatory cytokine IL-12 mRNA, however, did not differ among the three groups; IL-18 was expressed at lower levels in the lepromatous group than in the tuberculoid group and the noninfected group ( P < 0.0001). Moreover, the number of cells in which IL-18 mRNAs were detected by in situ hybridization was markedly decreased in the lepromatous group. These results indicate that the formation of lepromatous-type lesions or tuberculoid-type lesions may be influenced by alterations in Th1/Th2-type cytokine production and that IL-18 may play an important role in a Th1-to-Th2 switch in paratuberculosis.


1999 ◽  
Vol 10 (9) ◽  
pp. 1931-1939 ◽  
Author(s):  
TAE-SUN HA ◽  
JEFFREY L. BARNES ◽  
JENNIFER L. STEWART ◽  
CHEOL W. KO ◽  
JEFFREY H. MINER ◽  
...  

Abstract. This study examines the regulation of renal laminin in thedb/dbmouse, a model of type II diabetes characterized by extensive remodeling of extracellular matrix. Immunohistochemistry demonstrated an increase in the contents of laminin chains including β1 chain in the mesangium and tubular basement membranes at 1,2,3, and 4 mo of diabetes. Immunofluorescence with an antibody against the recently discovered laminin α5 chain showed that in the normal mouse, the protein had a restricted distribution to the glomerular and tubular basement membranes with scant expression in the mesangium of older mice. In the diabetic mouse, the laminin α5 chain content of the glomerular and tubular basement membranes was increased, with marked expression in the mesangium. Northern analysis revealed a significantdecreasein the renal cortical contents of α5, β1, and γ1 chain mRNA in the diabetic mice compared to control, at each of the time points.In situhybridization showed decreased abundance of α5 transcripts in the glomeruli of diabetic mice compared to nondiabetic controls. Analysis of mRNA changes by Northern andin situhybridization studies demonstrated that the reduction in laminin transcripts involved both glomerular and tubular elements. These observations demonstrate that laminin accumulation in thedb/dbmice with type II diabetes is due to nontranscriptional mechanisms. Because previous investigations in rodents with type I diabetes have shown that the increase in renal laminin content was associated with a corresponding increment in laminin chain transcript levels, it appears that the mechanisms underlying augmentation in renal matrix laminin content may be distinct in the two types of diabetes.


2003 ◽  
Vol 188 (7) ◽  
pp. 1024-1031 ◽  
Author(s):  
Mariane M. A. Stefani ◽  
Celina M. T. Martelli ◽  
Thomas P. Gillis ◽  
James L. Krahenbuhl ◽  

Sign in / Sign up

Export Citation Format

Share Document