Palojoki E, Toivanen P, Jalkanen S
Dept. of Medical Microbiology, Turku University, Finland.
Eur J Immunol. 1993 Mar;23(3):721-6. doi: 10.1002/eji.1830230323.
In chickens, the pre-B cell development takes place in a specialized organ, the bursa of Fabricius. In this study, we show that fibronectin can be detected in the bursa at least from the day 15 of embryonic incubation up to 10 weeks of age after which the bursa starts to involute. During the embryonic incubation, fibronectin localizes mainly in the areas between the follicles and later on also in the border zone between the cortical and medullary parts of the lymphoid follicles. By adhesion studies with synthetic peptides we show that immature bursal B cells bind in a dose-dependent manner to the CS-1 site of the type III connecting segment at the carboxy-terminal end of fibronectin throughout their bursal development. Postbursal B cells from chicken spleen also display a similar preference of binding to the CS-1 site of fibronectin, whereas peripheral blood B lymphocytes bind to the 40-kDa fragment of fibronectin, but do not adhere as strongly to the CS-1 site. Instead, they recognize to some extent also the heparin-binding YEKPGSPPREVVPRPRPGV peptide. The adhesion of the bursal B cells to the CS-1 site can partially be blocked by preincubation of cells with a synthetic CS-1 peptide and also by preincubation with a monoclonal anti-fibronectin receptor antibody. In contrast, the RGD motif present in several adhesion-associated stromal molecules did not promote any adherence of bursal lymphocytes. The bursal B cells which adhere to the fibronectin molecule in vitro form only a small fraction of the total number of B cells present in the bursa as only less than 4% of the cells remained bound to the surface coated with fibronectin in the adhesion studies. In conclusion, these results suggest that fibronectin may be involved in the differentiation of pre-B cells in the bursa of Fabricius and also in the adherence of postbursal B cells in the spleen.
在鸡体内,前B细胞的发育发生在一个特殊的器官——法氏囊中。在本研究中,我们发现至少从胚胎孵化第15天到10周龄,法氏囊中都能检测到纤连蛋白,10周龄后法氏囊开始退化。在胚胎孵化期间,纤连蛋白主要定位于滤泡之间的区域,之后也定位于淋巴滤泡皮质和髓质部分之间的边界区域。通过与合成肽的黏附研究,我们发现未成熟的法氏囊B细胞在其整个法氏囊发育过程中,以剂量依赖的方式与纤连蛋白羧基末端III型连接段的CS-1位点结合。来自鸡脾脏的囊后B细胞也表现出对纤连蛋白CS-1位点的类似结合偏好,而外周血B淋巴细胞则与纤连蛋白的40 kDa片段结合,但对CS-1位点的黏附不那么强烈。相反,它们在一定程度上也能识别肝素结合肽YEKPGSPPREVVPRPRPGV。法氏囊B细胞与CS-1位点的黏附可通过用合成CS-1肽预孵育细胞以及用抗纤连蛋白受体单克隆抗体预孵育而部分被阻断。相比之下,几种与黏附相关的基质分子中存在的RGD基序并未促进法氏囊淋巴细胞的任何黏附。在体外黏附于纤连蛋白分子的法氏囊B细胞仅占法氏囊中B细胞总数的一小部分,因为在黏附研究中只有不到4%的细胞仍与涂有纤连蛋白的表面结合。总之,这些结果表明纤连蛋白可能参与了法氏囊中前B细胞的分化以及脾脏中囊后B细胞的黏附。