scholarly journals Prss16 Is Not Required for T-Cell Development

2005 ◽  
Vol 25 (2) ◽  
pp. 789-796 ◽  
Author(s):  
Saijai Cheunsuk ◽  
Zhe-Xiong Lian ◽  
Guo-Xiang Yang ◽  
M. Eric Gershwin ◽  
Jeffrey R. Gruen ◽  
...  

ABSTRACT PRSS16 is a serine protease expressed exclusively in cortical thymic epithelial cells (cTEC) of the thymus, suggesting that it plays a role in the processing of peptide antigens during the positive selection of T cells. Moreover, the human PRSS16 gene is encoded in a region near the class I major histocompatibility complex (MHC) that has been linked to type 1 diabetes mellitus susceptibility. The mouse orthologue Prss16 is conserved in genetic structure, sequence, and pattern of expression. To study the role of Prss16 in thymic development, we generated a deletion mutant of Prss16 and characterized T-lymphocyte populations and MHC class II expression on cortical thymic epithelial cells. Prss16-deficient mice develop normally, are fertile, and show normal thymic morphology, cellularity, and anatomy. The total numbers and frequencies of thymocytes and splenic T-cell populations did not differ from those of wild-type controls. Surface expression of MHC class II on cTEC was also similar in homozygous mutant and wild-type animals, and invariant chain degradation was not impaired by deletion of Prss16. These findings suggest that Prss16 is not required for quantitatively normal T-cell development.

1996 ◽  
Vol 47 (1-2) ◽  
pp. 109
Author(s):  
Peter van den Elsen ◽  
Judy Henwood ◽  
Anette van Boxel-Dezaire ◽  
Ron Schipper ◽  
Martijn den Hoedt ◽  
...  

Immunity ◽  
2005 ◽  
Vol 23 (4) ◽  
pp. 375-386 ◽  
Author(s):  
Wei Li ◽  
Moon-Gyo Kim ◽  
Tania S. Gourley ◽  
Brian P. McCarthy ◽  
Derek B. Sant’Angelo ◽  
...  

2020 ◽  
Vol 11 ◽  
Author(s):  
Hong-Xia Wang ◽  
Wenrong Pan ◽  
Lei Zheng ◽  
Xiao-Ping Zhong ◽  
Liang Tan ◽  
...  

1994 ◽  
Vol 3 (4) ◽  
pp. 265-271 ◽  
Author(s):  
Eric J. Jenkinson ◽  
Graham Anderson ◽  
Nel C. Moore ◽  
Christopher A. Smith ◽  
John J. T. Owen

We have investigated the possibility that the costimulatory signals required for activation of mature T cells also play a role in providing differentiation signals for positive selection during T-cell development. We show that purified MHC Class II+thymic epithelial cells are able to support positive selectionin vitrobut lack both the functional capacity to deliver costimulatory signals and expression of the costimulatory ligand B7. Our results suggest that the additional signals provided by costimulatory ligands are not required for TCR-mediated positive selection, although other ancillary signals provided by thymic epithelial cells may be involved.


2003 ◽  
Vol 171 (8) ◽  
pp. 4096-4104 ◽  
Author(s):  
Claire Forestier ◽  
Se-Ho Park ◽  
Datsen Wei ◽  
Kamel Benlagha ◽  
Luc Teyton ◽  
...  

2012 ◽  
Vol 109 (51) ◽  
pp. 21040-21045 ◽  
Author(s):  
D. Ma ◽  
L. Wang ◽  
S. Wang ◽  
Y. Gao ◽  
Y. Wei ◽  
...  

Author(s):  
Rafael Gras-Pena ◽  
Nichole M. Danzl ◽  
Mohsen Khosravi-Maharlooei ◽  
Sean R. Campbell ◽  
Amanda E. Ruiz ◽  
...  

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