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15I5-B同基因系中的鸡发育抗原

Chicken developmental antigens in 15I5-B-congenic lines.

作者信息

Qureshi M A, Trembicki K A, Dietert R R, Bacon L D

出版信息

J Hered. 1986 Nov-Dec;77(6):435-40. doi: 10.1093/oxfordjournals.jhered.a110276.

Abstract

Six partially developed 15I5-B-congenic lines of chickens were used to assess the genetic influence on the developmental expression of selected epitopes of two avian developmental antigen systems: chicken fetal antigen (CFA) and chicken adult antigen (CAA). Both CFA and CAA are serologically and molecularly complex hematopoietic antigen systems, yet little is known about genetic influences on their expression. Using polyclonal rabbit anti-CFA, only slight variations in overall CFA expression on peripheral erythrocytes were observed during neonatal development; no consistent trend was evident. In contrast, analysis with monoclonal antibody 10C6 revealed that the incidence of CFA determinant 8 (CFA8) on erythrocytes of the early neonate was significantly reduced in line 15I5 compared with lines .6-2, .7-2 and .15I-5; line .C-12 also exhibited a reduced CFA8 incidence at hatching. Likewise, the CAA epitope detected by monoclonal antibody 3F12 was found to appear at a slower rate on erythrocytes from lines 15I5 and .C-12 than on those of other lines. Similar results were obtained using the anti-CAA monoclonal 4C2 where reduced expression was found in lines 15I5, .C-12, and .P-13. Results of complement-mediated cytolysis using the positive control 9F9 monoclonal antibody suggested that observed genetic differences were not due to inherent differences in erythroid cytolytic sensitivity. Neither could the results be explained by the incidence of circulating reticulocytes vs. mature erythrocytes within the lines. Rather, the results suggest that different genetic lines of chickens vary in the developmental kinetics of definitive erythrocyte subpopulations bearing specific phenotypes defined by monoclonal antibodies. These findings are discussed in light of previous observations using these B-congenic lines.

摘要

使用六个部分发育的15I5 - B - 同基因鸡系来评估遗传因素对两种禽类发育抗原系统(鸡胎儿抗原(CFA)和鸡成年抗原(CAA))选定表位发育表达的影响。CFA和CAA都是血清学和分子学上复杂的造血抗原系统,但关于遗传因素对其表达的影响知之甚少。使用多克隆兔抗CFA抗体,在新生期发育过程中,外周红细胞上CFA的整体表达仅观察到轻微变化;没有明显的一致趋势。相比之下,用单克隆抗体10C6分析发现,与6 - 2系、7 - 2系和15I - 5系相比,15I5系新生早期红细胞上CFA决定簇8(CFA8)的发生率显著降低;C - 12系在孵化时也表现出CFA8发生率降低。同样,发现单克隆抗体3F12检测到的CAA表位在15I5系和C - 12系红细胞上出现的速度比其他系的红细胞慢。使用抗CAA单克隆抗体4C2也得到了类似结果,在15I5系、C - 12系和P - 13系中发现表达降低。使用阳性对照9F9单克隆抗体进行补体介导的细胞溶解结果表明,观察到的遗传差异不是由于红细胞溶细胞敏感性的固有差异。这些结果也不能用各系中循环网织红细胞与成熟红细胞的发生率来解释。相反,结果表明不同遗传系的鸡在携带由单克隆抗体定义的特定表型的定型红细胞亚群的发育动力学方面存在差异。根据以前使用这些B - 同基因系的观察结果对这些发现进行了讨论。

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