Perlés B, Flanagan M T, Auger J, Crumpton M J
Eur J Immunol. 1977 Sep;7(9):613-9. doi: 10.1002/eji.1830070907.
The dynamics of phytohemagglutinin (PHA)-lymphocyte interaction was studied using 125I-labeled PHA (leucoagglutinin) and pig mesenteric lymph node lymphocytes that had been depleted of erythrocytes, dead cells, adherent cells and immunoglobulin-bearing cells. Evidence was obtained that PHA stimulated the majority of the lymphocytes to transform. Binding of PHA at 37 degrees C was fairly rapid (rate constant for association: 2.6 X 10(5) M-1 sec-1), saturable, reversible and specifically inhibited by N-acetylgalactosamine (Kdiss: 3 X 10(-4) M) and unlabeled PHA. A Scatchard plot was curvilinear and gave evidence for 3.6 X 10(5) binding sites per cell comprising 8.7% of high affinity sites (Kdiss: 3.7 X 10(-9) M) and 91.3% of lower affinity (Kdiss: 1.4 X 10(-7) M). About 20% of the sites were occupied under culture conditions giving maximal transformation. Alternative explanations for the curvilinear plot included negative cooperative interactions and/or increase in affinity through multivalent interaction. Negative cooperativity was supported by the demonstration that free PHA promoted the dissociation of bound PHA. Binding was not affected by metabolic inhibitors, and binding to purified lymphocyte plasma membrane resembled that to whole cells. These results suggested that PHA binding to whole lymphocytes was not grossly influenced by "capping", endocytosis and shedding.
利用125I标记的植物血凝素(PHA,白细胞凝集素)和去除了红细胞、死细胞、贴壁细胞及免疫球蛋白携带细胞的猪肠系膜淋巴结淋巴细胞,研究了PHA与淋巴细胞相互作用的动力学。结果表明,PHA能刺激大多数淋巴细胞发生转化。PHA在37℃时的结合相当迅速(结合速率常数:2.6×10⁵M⁻¹s⁻¹),具有饱和性、可逆性,且能被N - 乙酰半乳糖胺(解离常数:3×10⁻⁴M)和未标记的PHA特异性抑制。Scatchard图呈曲线,表明每个细胞有3.6×10⁵个结合位点,其中8.7%为高亲和力位点(解离常数:3.7×10⁻⁹M),91.3%为低亲和力位点(解离常数:1.4×10⁻⁷M)。在能使转化达到最大值的培养条件下,约20%的位点被占据。对曲线图谱的其他解释包括负协同相互作用和/或通过多价相互作用导致亲和力增加。游离PHA能促进结合的PHA解离,这一现象支持了负协同作用。结合不受代谢抑制剂的影响,并且与纯化的淋巴细胞质膜的结合类似于与全细胞的结合。这些结果表明,PHA与全淋巴细胞的结合不受“帽化”、内吞作用和脱落的严重影响。