Kalataradi H, Eyster C L, Fry A, Vollmer M K, Fu Y X, Born W K, O'Brien R L
National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
J Immunol. 1994 Aug 15;153(4):1455-65.
Mouse gamma delta T cell hybridomas from various strains that express a TCR-V gamma 1/V delta 6 respond weakly to an autologous Ag and more strongly to a short segment of the mycobacterial heat shock protein-60 (HSP-60). However, V gamma 1/V delta 6 hybridomas derived from AKR mice show greatly reduced or absent responses to these stimuli. To determine whether the lack of response in these AKR hybridomas is caused by polymorphisms found in the expressed AKR gamma and TCR-delta genes or, instead, stems from other genes in AKR, we crossed an AKR mouse with a responder mouse, C57BL/10 (B10), and prepared hybridomas from F1 progeny. Expression of an AKR V gamma 1-J gamma 4-C gamma 4 gene correlated with nonresponsiveness, whereas expression of a B10 V gamma 1-J gamma 4-C gamma 4 gene in most hybridomas ensured responses to both self Ag and the HSP-60 peptide. An allelic difference in the expressed V gamma 6 gene was irrelevant to these responses. Moreover, transfection of a functional B10 V gamma 1-J gamma 4-C gamma 4 gene into an F1 hybridoma variant that had lost the AKR version of this gene restored responses. The allelic gamma gene products differ at nine amino acids in the V region, and three amino acids in the C region. In addition, the AKR C gamma 4 region contains a 16-amino acid insertion. We propose that amino acid differences among those encoded by the AKR V gamma 1-J gamma 4-C gamma 4 gene are responsible for the lack of response, and reduce the ability of the TCR-gamma delta to bind the relevant Ag.
来自不同品系、表达TCR-Vγ1/Vδ6的小鼠γδT细胞杂交瘤对自身抗原反应较弱,而对分枝杆菌热休克蛋白-60(HSP-60)的短片段反应较强。然而,源自AKR小鼠的Vγ1/Vδ6杂交瘤对这些刺激的反应大大降低或完全没有反应。为了确定这些AKR杂交瘤缺乏反应是由表达的AKRγ和TCR-δ基因中的多态性引起的,还是源于AKR中的其他基因,我们将一只AKR小鼠与一只反应性小鼠C57BL/10(B10)杂交,并从F1后代中制备杂交瘤。AKR Vγ1-Jγ4-Cγ4基因的表达与无反应性相关,而大多数杂交瘤中B10 Vγ1-Jγ4-Cγ4基因的表达确保了对自身抗原和HSP-60肽的反应。表达的Vγ6基因中的等位基因差异与这些反应无关。此外,将功能性B10 Vγ1-Jγ4-Cγ4基因转染到一个丢失了该基因的AKR版本的F1杂交瘤变体中,恢复了反应。等位基因γ基因产物在V区有9个氨基酸不同,在C区有3个氨基酸不同。此外,AKR Cγ4区域包含一个16个氨基酸的插入。我们提出,AKR Vγ1-Jγ4-Cγ4基因编码的氨基酸差异是导致无反应性的原因,并降低了TCR-γδ结合相关抗原的能力。