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  4. Abnormal Splenic and Thymic IL‐4 and TNF‐α Expression in MRL‐lpr/lpr Mice
 
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Abnormal Splenic and Thymic IL‐4 and TNF‐α Expression in MRL‐lpr/lpr Mice

Journal
Scandinavian Journal of Immunology
Journal Volume
41
Journal Issue
2
Pages
157-163
Date Issued
1995
Author(s)
TSAI C.‐Y.
WU T.‐H.
HUANG S.‐F.
SUN K.‐H.
SONG-CHOU HSIEH  
HAN S.‐H.
YU H.‐S.
CHIA-LI YU  
DOI
10.1111/j.1365-3083.1995.tb03548.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028955030&doi=10.1111%2fj.1365-3083.1995.tb03548.x&partnerID=40&md5=f5d3baf4e7d0cb63bba41ecabddcfc9a
https://scholars.lib.ntu.edu.tw/handle/123456789/540888
Abstract
The MRL-lpr/lpr and MRL-(++) mice were studied for the expression of cytokines in the spleen, lymph node, thymus, kidney and brain through the reverse transcription-polymerase chain reaction (RT-PCR). The frequencies of IL-4 and TNF-alpha expression in the thymus and spleen were significantly higher in MRL-lpr/lpr mice than in MRL-(++) mice from the age of 17 to 32 weeks. More importantly, IL-4 transcript was demonstrated in the early rather than in the terminal stage of the lupus disease. At the 20th week, MRL-lpr/lpr mice with active disease exhibited higher concentrations of IL-1 alpha, IL-6 and TNF-alpha in serum than MRL-(++) mice. Interestingly, in MRL-lpr/lpr but not MRL-(++) mice, the IL-6 concentration in cultured supernatants of the thymic cells was significantly higher than that of the splenic or lymph node cells. On the other hand, IL-6 and IL-1 beta were expressed in the brain and kidney of MRL-lpr/lpr mice but not of MRL-(++) mice. Cultured MRL-lpr/lpr mesangial cells could also express IL-6 but to a lesser extent. These results suggest that the abnormal splenic and thymic IL-4 and TNF-alpha expression may predispose the development of autoimmune reactions. The expression of IL-1 beta and IL-6 in the brain and kidney may be implicated in the damage of these two organs in MRL-lpr/lpr mice.
SDGs

[SDGs]SDG3

Type
journal article

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