FAHEY J L, SELL S
J Exp Med. 1965 Jul 1;122(1):41-58. doi: 10.1084/jem.122.1.41.
The metabolic properties of immunoglobulin were investigated by comparing five classes of mouse immunoglobulin. Three forms of 7S immunoglobulin had different rates of catabolism. The fractional rates of catabolism were found to be about 13 per cent per day for 7S gamma(2a)-globulin; 25 per cent for 7S gamma(2b)-globulin; and 17 per cent for 7S gamma(1)-globulin. Catabolism of the three classes of 7S gamma-globulin (gamma(2a), gamma(2b), and gamma(1)) were prolonged at low serum 7S gamma-globulin levels and accelerated at high serum 7S gamma-globulin levels. Each of the 7S gamma-globulin components was influenced by the serum level of the other mouse 7S gamma-globulin components and by exogenously administered human 7S gamma-globulin. They were not appreciably altered, however, by the serum level of IgA (gamma(1)A-, beta(2)A-globulin). The progressively changing (longer) half-times observed in turnover studies of normal IgG (7S gamma-globulin) may be caused by catabolic heterogeneity of normal 7S immunoglobulins which are immunochemically and catabolically related to gamma(2a)-, gamma(2b)-, and 7S gamma(1)-myeloma proteins. These studies indicate that the 7S gamma(2a)-, 7S gamma(2b)-, and 7S gamma(1)-globulins share a common catabolic control mechanism. This mechanism is influenced by the serum level of each of these components, but is independent of the serum level of IgA (gamma(1)A-globulin) and probably is independent of IgM (gamma(1)M-globulin). Catabolism of IgA (gamma(1)A-, beta(2)A-globulin) and IgM (gamma(1)M-globulin) was much more rapid than the catabolism of the 7S gamma-globulins. The halftimes of the IgA and IgM were approximately 1.2 and 0.5 days respectively. The fractional rate of catabolism of IgA and IgM seemed to be independent of their serum concentration. The rate of catabolism, as well as the rate of synthesis, was shown to play a major role in determining the serum level of each class of immunoglobulin.
通过比较五类小鼠免疫球蛋白,对免疫球蛋白的代谢特性进行了研究。三种形式的7S免疫球蛋白具有不同的分解代谢速率。发现7Sγ(2a)球蛋白的分解代谢分数率约为每天13%;7Sγ(2b)球蛋白为25%;7Sγ(1)球蛋白为17%。三类7Sγ球蛋白(γ(2a)、γ(2b)和γ(1))在血清7Sγ球蛋白水平较低时分解代谢延长,在血清7Sγ球蛋白水平较高时加速。7Sγ球蛋白的每一种成分都受到其他小鼠7Sγ球蛋白成分的血清水平以及外源性给予的人7Sγ球蛋白的影响。然而,它们并未因IgA(γ(1)A-、β(2)A球蛋白)的血清水平而发生明显改变。在正常IgG(7Sγ球蛋白)周转研究中观察到的逐渐变化(更长)的半衰期,可能是由正常7S免疫球蛋白的分解代谢异质性引起的,这些免疫球蛋白在免疫化学和分解代谢上与γ(2a)-、γ(2b)-和7Sγ(1)-骨髓瘤蛋白相关。这些研究表明,7Sγ(2a)-、7Sγ(2b)-和7Sγ(1)-球蛋白共享一种共同的分解代谢控制机制。这种机制受这些成分中每一种的血清水平影响,但独立于IgA(γ(1)A球蛋白)的血清水平,可能也独立于IgM(γ(1)M球蛋白)。IgA(γ(1)A-、β(2)A球蛋白)和IgM(γ(1)M球蛋白)的分解代谢比7Sγ球蛋白的分解代谢快得多。IgA和IgM的半衰期分别约为1.2天和0.5天。IgA和IgM的分解代谢分数率似乎与其血清浓度无关。分解代谢速率以及合成速率在决定每类免疫球蛋白的血清水平中起着主要作用。