O'Bryan M K, Grima J, Mruk D, Cheng C Y
The Population Council, Center for Biomedical Research, New York, New York 10021, USA.
J Androl. 1997 Nov-Dec;18(6):637-45.
Using multiple HPLC steps, a protein of 67 kDa (estimated by gel permeation HPLC) was purified from Sertoli cell-enriched culture medium that consisted of two dissimilar subunits of 9 (alpha chain) and 24 (beta chain) kDa on SDS-polyacrylamide under reducing conditions. Direct protein sequence analysis of the 9-kDa subunit revealed a sequence of NH2-VELGNDATDIEXD, which is identical to the alpha subunit of the rat haptoglobin (Hp). Hp is a 67-kDa tetrameric serum acute-phase protein consisting of two alpha and two beta subunits (alpha2beta2) of 8.5 kDa and 24.5 kDa, respectively. Using a 351-bp cDNA coding for Hp for northerns and two Hp primers for RT-PCR, we have demonstrated the expression of Hp in Sertoli and Leydig cells, germ cells, and the testis, but not in the epididymis. In contrast to the hepatic haptoglobin, an acute-phase protein whose steady-state mRNA level increased by as much as fivefold during induced inflammation, the testicular homolog reduced by fourfold within 24 hours following induced inflammation, suggesting that this gene is regulated differently in the testis and in the liver. Moreover, the testicular steady-state Hp mRNA level increased steadily after birth during maturation, suggesting its involvement in spermatogenesis. Using primary Sertoli cell cultures in vitro, it was found that the Sertoli cell Hp expression was not regulated by either FSH, testosterone, estradiol, dexamethasone, interleukin-1beta (IL-1beta), IL-6, interferon-gamma (INF-gamma), transforming growth factor-beta (TGF-beta), lymphocyte inhibitory factor (LIF), or germ-cell-conditioned medium (GCCM). Since transferrin secreted by Sertoli cells is an important molecule in maintaining the crucial iron level necessary for spermatogenesis, the identification of haptoglobin as a Sertoli and germ cell product adds a new member to the growing family of metal transporters in the testis that are likely to play an important role in iron metabolism in the testis.
通过多个高效液相色谱步骤,从富含支持细胞的培养基中纯化出一种67 kDa的蛋白质(通过凝胶渗透高效液相色谱估计),在还原条件下,该蛋白质在SDS聚丙烯酰胺凝胶上由9 kDa(α链)和24 kDa(β链)的两个不同亚基组成。对9 kDa亚基进行直接蛋白质序列分析,结果显示其序列为NH2-VELGNDATDIEXD,与大鼠触珠蛋白(Hp)的α亚基相同。Hp是一种67 kDa的四聚体血清急性期蛋白,分别由两个8.5 kDa和24.5 kDa的α亚基和β亚基(α2β2)组成。使用编码Hp的351 bp cDNA进行Northern杂交以及两个用于RT-PCR的Hp引物,我们证明了Hp在支持细胞、间质细胞、生殖细胞和睾丸中表达,但在附睾中不表达。与肝脏触珠蛋白不同,肝脏触珠蛋白是一种急性期蛋白,其稳态mRNA水平在诱导炎症期间可增加多达五倍,而睾丸中的同源物在诱导炎症后24小时内降低了四倍,这表明该基因在睾丸和肝脏中的调控方式不同。此外,睾丸稳态Hp mRNA水平在出生后的成熟过程中稳步上升,表明其参与精子发生。在体外使用原代支持细胞培养发现,支持细胞中Hp的表达不受促卵泡激素、睾酮、雌二醇、地塞米松、白细胞介素-1β(IL-1β)、IL-6、干扰素-γ(INF-γ)、转化生长因子-β(TGF-β)、淋巴细胞抑制因子(LIF)或生殖细胞条件培养基(GCCM)的调节。由于支持细胞分泌的转铁蛋白是维持精子发生所需关键铁水平的重要分子,触珠蛋白作为支持细胞和生殖细胞产物的鉴定为睾丸中不断增加的金属转运蛋白家族增添了新成员,这些金属转运蛋白可能在睾丸铁代谢中发挥重要作用。