Su Linlin, Mruk Dolores D, Cheng C Yan
The Mary M. Wohlford Laboratory for Male Contraceptive Research; Center for Biomedical Research; Population Council; New York, NY USA.
Spermatogenesis. 2012 Oct 1;2(4):285-293. doi: 10.4161/spmg.22536.
The blood-testis barrier (BTB) provides an efficient barrier to restrict paracellular and transcellular transport of substances, such as toxicants and drugs, limiting their entry to the testis to cause injury. This is achieved by the coordinated actions of efflux and influx transporters at the BTB, which are integral membrane proteins that interact with their substrates, such as drugs and toxicants. An efflux transporter (e.g., P-glycoprotein) can either restrict the entry of drugs/toxicants into the testis or actively pump drugs/toxicants out of Sertoli and/or germ cells if they have entered the seminiferous epithelium via influx pumps. This thus provides an effective mechanism to safeguard spermatogenesis. Using Sertoli cells cultured in vitro with an established tight junction (TJ)-permeability barrier which mimicked the BTB in vivo and treated with cadmium chloride (CdCl2), and also in adult rats (~300 g b.w.) treated with CdCl2 (3 mg/kg b.w., via i.p.) to induce testicular injury, cadmium was found to significantly downregulate the expression of efflux (e.g., P-glycoprotein, Mrp1, Abcg1) and influx (e.g., Oatp3, Slc15a1, Scl39a8) transporters. For instance, treatment of Sertoli cells with cadmium induced significant loss of P-glycoprotein and Oatp-3 at the cell-cell interface, which likely facilitated cadmium entry into the Sertoli cell. These findings illustrate that one of the mechanisms by which cadmium enters the testis is mediated by downregulating the expression of drug transporters at the BTB. Furthermore, cytokines and steroids were found to have differential effects in regulating the expression of drug transporters. Summary, the expression of drug transporters in the testis is regulated by toxicants, steroids and cytokines.
血睾屏障(BTB)形成了一道有效的屏障,可限制诸如毒物和药物等物质的细胞旁转运和跨细胞转运,从而限制它们进入睾丸并造成损伤。这是通过BTB处外排转运蛋白和内流转运蛋白的协同作用实现的,这些转运蛋白是与药物和毒物等底物相互作用的整合膜蛋白。外排转运蛋白(如P-糖蛋白)既可以限制药物/毒物进入睾丸,也可以在药物/毒物通过内流泵进入生精上皮后,将其主动泵出支持细胞和/或生殖细胞。因此,这提供了一种保护精子发生的有效机制。利用体外培养的具有紧密连接(TJ)通透性屏障的支持细胞,该屏障模拟体内的BTB,并使用氯化镉(CdCl2)进行处理,以及在成年大鼠(体重约300 g)中通过腹腔注射CdCl2(3 mg/kg体重)诱导睾丸损伤,结果发现镉可显著下调外排转运蛋白(如P-糖蛋白、Mrp1、Abcg1)和内流转运蛋白(如Oatp3、Slc15a1、Scl39a8)的表达。例如,用镉处理支持细胞会导致细胞间界面处P-糖蛋白和Oatp-3显著减少,这可能促进了镉进入支持细胞。这些发现表明,镉进入睾丸的机制之一是通过下调BTB处药物转运蛋白的表达来介导的。此外,还发现细胞因子和类固醇在调节药物转运蛋白的表达方面具有不同的作用。总之,睾丸中药物转运蛋白的表达受毒物、类固醇和细胞因子的调节。