Hoermann R, Amir S M, Nomura T, Ingbar S H
Charles A. Dana Research Institute, Harvard Thorndike Laboratory, Boston, Massachusetts.
Endocrinology. 1989 Jan;124(1):223-32. doi: 10.1210/endo-124-1-223.
Previous studies have revealed that desialylated forms of hCG have a high potency to inhibit both the binding of bovine TSH (bTSH) to human thyroid membranes and the bTSH-stimulated adenylate cyclase activity therein. The biological activities of these desialylated forms, however, are greatly reduced in vivo due to the high affinity of asialo-glycoproteins for hepatic receptors and their consequent rapid clearance from the circulation. Intact purified hCG (hCGp), on the other hand, has little affinity for hepatic receptors and has a relatively long half-life in vivo, but displays only negligible inhibitory potency in the human thyroid. In the present studies, we have sought to obtain one or more compounds derived from hCG that are able to inhibit binding to TSH to the high affinity receptor in human thyroid membranes, and, consequently, could inhibit the stimulatory effect of TSH and Graves' immunoglobulin G and which also display a relatively low affinity for the hepatic asialoglycoprotein receptor and, as a consequence, have a reasonable survival in the circulation. Two hCG forms isolated by sequential chromatography of crude hCG on DEAE-52 and Sephadex G-100 were of interest, since they displayed some degree of selectivity in binding to thyroid and liver receptors. The first form (hCGv), whose isolation we described previously, was comprised of partially desialylated variant forms of intact hCG. The second material, as judged from its immunoreactivity, elution behavior on Bio-Gel P-100, and migration during sodium dodecyl sulfate-polyacrylamide gel electrophoresis, contained a fragment of the beta-subunit (BF), similar to the beta-core fragment described by others. However, BF differed from the beta-core fragment in having a higher sialic acid content. Interestingly, we found that BF as well as the enzymatically desialylated form of BF displayed a much lower affinity for mouse liver receptors than did asialo-hCGp or the free asialo-beta- and asialo-alpha-subunits. Further, the activity of BF to inhibit the binding of [125I]bTSH to human thyroid membranes exceeded that of the desialylated subunits of hCGp as well as that of intact hCGp, but was only exerted at the low affinity binding site and was not accompanied by inhibition of TSH-stimulated adenylate cyclase. In an attempt to shift the locus of BF action from the low to the high affinity TSH receptor, we recombined BF with either an intact alpha-subunit of hCG or an asialo-alpha-subunit. This led to the creation of two novel forms of hCG with properties of the type that we were seeking.(ABSTRACT TRUNCATED AT 400 WORDS)
先前的研究表明,去唾液酸化形式的人绒毛膜促性腺激素(hCG)具有高效抑制牛促甲状腺激素(bTSH)与人甲状腺膜结合以及bTSH刺激的腺苷酸环化酶活性的能力。然而,由于去唾液酸糖蛋白对肝受体具有高亲和力,这些去唾液酸化形式的生物活性在体内会大大降低,从而导致它们从循环中迅速清除。另一方面,完整纯化的hCG(hCGp)对肝受体的亲和力很低,在体内具有相对较长的半衰期,但在人甲状腺中仅表现出可忽略不计的抑制效力。在本研究中,我们试图获得一种或多种源自hCG的化合物,这些化合物能够抑制TSH与人甲状腺膜中高亲和力受体的结合,因此能够抑制TSH和格雷夫斯病免疫球蛋白G的刺激作用,并且对肝去唾液酸糖蛋白受体也表现出相对较低的亲和力,结果在循环中具有合理的存活时间。通过在DEAE - 52和Sephadex G - 100上对粗制hCG进行连续层析分离得到的两种hCG形式令人感兴趣,因为它们在与甲状腺和肝受体结合方面表现出一定程度的选择性。第一种形式(hCGv),我们之前已描述过其分离过程,由完整hCG的部分去唾液酸化变体形式组成。从其免疫反应性、在Bio - Gel P - 100上的洗脱行为以及在十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳中的迁移情况判断,第二种物质包含β亚基的一个片段(BF),类似于其他人描述的β核心片段。然而,BF与β核心片段的不同之处在于其唾液酸含量更高。有趣的是,我们发现BF以及BF的酶促去唾液酸化形式对小鼠肝受体的亲和力远低于去唾液酸hCGp或游离的去唾液酸β亚基和去唾液酸α亚基。此外,BF抑制[125I]bTSH与人甲状腺膜结合的活性超过了hCGp的去唾液酸化亚基以及完整hCGp的活性,但仅在低亲和力结合位点发挥作用,且不伴随对TSH刺激的腺苷酸环化酶的抑制。为了将BF的作用位点从低亲和力TSH受体转移到高亲和力TSH受体,我们将BF与hCG的完整α亚基或去唾液酸α亚基进行重组。这导致产生了两种具有我们所寻求类型特性的新型hCG形式。(摘要截短至400字)