L'age-Stehr J, Herzenberg L A
J Exp Med. 1970 Jun 1;131(6):1093-108. doi: 10.1084/jem.131.6.1093.
Plaque forming cells (PFC) of different immunoglobulin classes producing antibodies against sheep erythrocytes were separated according to their buoyant densities by means of equilibrium centrifugation in a stepwise BSA gradient. In the period of 7-10 days after immunization gammaM PFC are markedly enriched in fractions of low density and relatively depleted in fractions of high density. The distribution of total gammaG PFC shows less enrichment in the lower density fractions and less depletion in the higher density fractions. The density profile for gammaG(2a) PFC is even flatter, with a significant difference (depletion) relative to the unseparated spleen cells only in the highest density fraction. The density gradient distributions of cells able to transfer an adoptive immune response of the various immunoglobulin classes are markedly different from the PFC distribution. Cells obtained 7-10 days after immunization able to transfer an IgM response are present in the same proportions across the density gradient, whereas memory cells for gammaG(2a) obtained at this time are markedly enriched in fractions of low density and virtually depleted from high density fractions. With increasing time after primary immunization, the gammaG(2a) memory cells increase progressively in density and by 6 weeks the higher and lower density fractions have the same proportions of gammaG(2a) memory cells. The total gammaG (mainly gammaG(1)) memory cells by 7-10 days show slight enrichment in low density fractions and no depletion in high density fractions. The conclusions were reached that (a) memory for gammaG(1) develops earlier than memory for gammaG(2a) and (b) that memory for anti-SRBC antibodies of different classes is carried in separate cells. When gradient fractions enriched for PFC and memory cells for all classes were completely depleted of PFC using glass bead columns, the ability of this fraction to transfer memory for all classes was not diminished. This shows that memory cells are not identical with cells secreting antibodies.
通过在逐步的牛血清白蛋白梯度中进行平衡离心,根据其浮力密度分离出产生抗绵羊红细胞抗体的不同免疫球蛋白类别的斑块形成细胞(PFC)。在免疫后7至10天期间,γM PFC在低密度组分中显著富集,而在高密度组分中相对减少。总γG PFC的分布在较低密度组分中的富集较少,在较高密度组分中的减少也较少。γG(2a) PFC的密度分布更为平坦,仅在最高密度组分中相对于未分离的脾细胞有显著差异(减少)。能够传递各种免疫球蛋白类别的过继免疫反应的细胞的密度梯度分布与PFC分布明显不同。免疫后7至10天获得的能够传递IgM反应的细胞在整个密度梯度中以相同比例存在,而此时获得的γG(2a)记忆细胞在低密度组分中显著富集,在高密度组分中几乎没有。随着初次免疫后时间的增加,γG(2a)记忆细胞的密度逐渐增加,到6周时,高密度和低密度组分中γG(2a)记忆细胞的比例相同。到7至10天时,总γG(主要是γG(1))记忆细胞在低密度组分中略有富集,在高密度组分中没有减少。得出的结论是:(a)γG(1)的记忆比γG(2a)的记忆发展得更早;(b)不同类别的抗SRBC抗体的记忆存在于不同的细胞中。当使用玻璃珠柱将富含所有类别的PFC和记忆细胞的梯度组分中的PFC完全去除时,该组分传递所有类别的记忆的能力并未减弱。这表明记忆细胞与分泌抗体的细胞不同。