immune system
• BrdU incorporation of double-negative (DN) T cells is 15.1% versus 26.6% in controls, indicating that cell proliferation accompanied with DN-to-DP transition after beta-selection is suppressed
• Cdkn1a (p21Cip1) mRNA expression is increased in DN3 (Lin-CD25+CD117-) populations
• however, expression of Myc (c-Myc) mRNA and protein in DN3 is normal
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• early T-cell precursor (ETP) numbers are significantly reduced
• total thymocyte number is reduced by ~25-fold
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• abnormal differentiation from DN3a to DN3b and DN4 compartments
• however, DNA rearrangement of the TCRbeta locus is normal
|
• % of intracellular TCRbeta (icTCRb)+ cells in DN4 is reduced
• however, % of icTCRb+ cells in DN3 is normal
|
• DN3 thymocyte number is reduced by >2.5-fold
• % of DN3b cells (defined by CD27hi and increased cell size) in DN3 population is decreased while upregulation of CD27 expression is reduced, suggesting defects in pre-TCR signaling
• however, % of intracellular TCRbeta (icTCRb)+ cells in DN3 is normal
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• DN4 thymocyte number is reduced by 20-fold
• % of intracellular TCRbeta (icTCRb)+ cells in DN4 is reduced
|
• severe block in the transition from the double-negative DN3/4 stage to the double-positive (DP) stage
• most cells accumulate at the DN3 (CD25+CD117-) stage where beta-selection occurs
• however, Notch signaling is not impaired at the DN3 stage and gamma-delta T cell development is normal
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• significant decrease in CD4 single-positive (SP) population
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• significant decrease in CD8 immature single-positive (SP) population
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hematopoietic system
• BrdU incorporation of double-negative (DN) T cells is 15.1% versus 26.6% in controls, indicating that cell proliferation accompanied with DN-to-DP transition after beta-selection is suppressed
• Cdkn1a (p21Cip1) mRNA expression is increased in DN3 (Lin-CD25+CD117-) populations
• however, expression of Myc (c-Myc) mRNA and protein in DN3 is normal
|
• early T-cell precursor (ETP) numbers are significantly reduced
• total thymocyte number is reduced by ~25-fold
|
• abnormal differentiation from DN3a to DN3b and DN4 compartments
• however, DNA rearrangement of the TCRbeta locus is normal
|
• % of intracellular TCRbeta (icTCRb)+ cells in DN4 is reduced
• however, % of icTCRb+ cells in DN3 is normal
|
• DN3 thymocyte number is reduced by >2.5-fold
• % of DN3b cells (defined by CD27hi and increased cell size) in DN3 population is decreased while upregulation of CD27 expression is reduced, suggesting defects in pre-TCR signaling
• however, % of intracellular TCRbeta (icTCRb)+ cells in DN3 is normal
|
• DN4 thymocyte number is reduced by 20-fold
• % of intracellular TCRbeta (icTCRb)+ cells in DN4 is reduced
|
• severe block in the transition from the double-negative DN3/4 stage to the double-positive (DP) stage
• most cells accumulate at the DN3 (CD25+CD117-) stage where beta-selection occurs
• however, Notch signaling is not impaired at the DN3 stage and gamma-delta T cell development is normal
|
• significant decrease in CD4 single-positive (SP) population
|
• significant decrease in CD8 immature single-positive (SP) population
|
endocrine/exocrine glands
• early T-cell precursor (ETP) numbers are significantly reduced
• total thymocyte number is reduced by ~25-fold
|
• DN3 thymocyte number is reduced by >2.5-fold
• % of DN3b cells (defined by CD27hi and increased cell size) in DN3 population is decreased while upregulation of CD27 expression is reduced, suggesting defects in pre-TCR signaling
• however, % of intracellular TCRbeta (icTCRb)+ cells in DN3 is normal
|
• DN4 thymocyte number is reduced by 20-fold
• % of intracellular TCRbeta (icTCRb)+ cells in DN4 is reduced
|
cellular
• BrdU incorporation of double-negative (DN) T cells is 15.1% versus 26.6% in controls, indicating that cell proliferation accompanied with DN-to-DP transition after beta-selection is suppressed
• Cdkn1a (p21Cip1) mRNA expression is increased in DN3 (Lin-CD25+CD117-) populations
• however, expression of Myc (c-Myc) mRNA and protein in DN3 is normal
|