Fragoso A, Arciga M A, Calcagno M, Weiss-Steider B
Exp Hematol. 1985 Mar;13(3):163-8.
The presence of factors responsible for the induction of Fc receptors (FcRI) and C3 receptors (C3RI) on mouse myeloid cells was determined in postendotoxin serum and in media conditioned by postendotoxin lungs, peritoneal macrophages, peritoneal granulocytes, and lymphocytes from either the lymph nodes, the thymus, or the spleen, FcRI and C3RI were found only in postendotoxin serum and in media conditioned by either postendotoxin lungs or peritoneal macrophages. The apparent molecular weights obtained by molecular sieving chromatography in Sephadex G-100 were 10,500 daltons for FcRI and 35,000 daltons for C3RI. These results suggest the existence of several molecules responsible for induction of Fc and C3 receptors. Under our experimental conditions, the macrophage was the only blood cell capable of FcRI and C3RI production, thus hinting at a possible feedback regulatory mechanism. In order to determine whether both inducing factors are also present in normal individuals, human serum and urine were used. FcRI and C3RI were both found in human serum, while only the FcRI factor was detected in urine. These results indicate that the normal human being produces FcRI and C3RI, and that probably the C3RI does not pass through the kidney barrier. The mechanism of action of these factors can be studied by using mouse cells.
在内毒素血症后的血清以及由内毒素血症后的肺、腹膜巨噬细胞、腹膜粒细胞和来自淋巴结、胸腺或脾脏的淋巴细胞所产生的条件培养基中,测定了诱导小鼠髓样细胞上Fc受体(FcRI)和C3受体(C3RI)的因子的存在情况。仅在内毒素血症后的血清以及由内毒素血症后的肺或腹膜巨噬细胞所产生的条件培养基中发现了FcRI和C3RI。通过在Sephadex G - 100中进行分子筛层析获得的表观分子量,FcRI为10,500道尔顿,C3RI为35,000道尔顿。这些结果表明存在几种负责诱导Fc和C3受体的分子。在我们的实验条件下,巨噬细胞是唯一能够产生FcRI和C3RI的血细胞,因此暗示了一种可能的反馈调节机制。为了确定正常个体中是否也存在这两种诱导因子,使用了人血清和尿液。在人血清中同时发现了FcRI和C3RI,而在尿液中仅检测到FcRI因子。这些结果表明正常人会产生FcRI和C3RI,并且可能C3RI不会穿过肾脏屏障。这些因子的作用机制可以通过使用小鼠细胞来研究。