Grimaldi S, Lio S, Iacovacci P, Carlini F, Monaco F, Roche J
C R Seances Soc Biol Fil. 1986;180(3):277-83.
Two kinds of TBG polymorphism are described in human, one found in deglycosylated TBG from individual blood donors, the other is a genetically determined polymorphism. TBG from plasma samples from a patient with toxic goiter, not autoimmune, (p)TBG, from the patient's mother (m)TBG and from individual donors (n)TBG, were labeled with [125I]T4 or [125I]T3 and submitted to isoelectric focusing (IEF), followed by autoradiography. Three faint [125I]T4 radiolabeled bands were detectable in (p)TBG while four strong [125I]T4 radiolabeled bands were detectable in (m)TBG and (n)TBG), respectively. IEF of the [125I]T3 incubated serum samples resulted in no detectable isoelectric radiolabeled band for (p)TBG while a normal pattern was found in (m)TBG and in (n)TBG, respectively. These data suggest a new intraindividual not linked to sexual chromosome X polymorphism characterized by a loss in hormone binding.
人类中描述了两种甲状腺素结合球蛋白(TBG)多态性,一种存在于个体献血者的去糖基化TBG中,另一种是由基因决定的多态性。来自一名非自身免疫性毒性甲状腺肿患者的血浆样本中的TBG(pTBG)、患者母亲的TBG(mTBG)和个体献血者的TBG(nTBG),用[125I]T4或[125I]T3进行标记,然后进行等电聚焦(IEF),接着进行放射自显影。在pTBG中可检测到三条 faint [125I]T4放射性标记带,而在mTBG和nTBG中分别可检测到四条强的[125I]T4放射性标记带。[125I]T3孵育的血清样本的IEF结果显示,pTBG未检测到等电放射性标记带,而mTBG和nTBG分别呈现正常模式。这些数据表明存在一种新的个体内多态性,与X性染色体无关,其特征是激素结合能力丧失。