Hellmann P, Winterhager E, Spray D C
Institute of Anatomy, Medical School, University of Essen, D-45122 Essen, Germany.
Pflugers Arch. 1996 Jul;432(3):501-9. doi: 10.1007/s004240050162.
We have investigated the properties of gap junction channels of three human malignant trophoblast (choriocarcinoma) cell lines: BeWo, Jeg-3 and JAr, as well as in Jeg-3 cells stably transfected with rat connexin40 (Cx40). Reverse-transcriptase polymerase chain reaction (RT-PCR), Northern blot analysis and immunostaining demonstrated expression of Cx40 in BeWo and JAr cell lines. JAr cells also expressed minor amounts of Cx43. Very low levels of Cx40 transcripts were revealed by RT-PCR in parental Jeg-3 cells, but Cx40 protein was not detected. To compare properties of endogenously and exogenously expressed Cx40 channels we have transfected Jeg-3 cells with rat Cx40. Recordings with dual whole-cell methods were used to determine the junctional conductance (gj) in the various cell lines and transfectants. Cx40 channels exogenously expressed in Jeg-3 cells demonstrated steep voltage sensitivity in the transjunctional voltage range of +/-30 to +/-40 mV and a unitary mainstate conductance of 175 pS, values which are similar to the data obtained from endogenously expressed Cx40 in BeWo cell pairs. In addition, greater driving forces resulted in a lower unitary conductance of about 30 pS, exclusively in BeWo cells. Between JAr cell pairs we determined a gj of 10 nS and unitary conductances were predominantly 100 and 152 pS. Voltage dependence was less sensitive in JAr cells compared to Cx40 transfectants and BeWo cells. Thus, coexpression of Cx43 and Cx40 leads to a macroscopic conductance with a mixture of properties expected for each connexin, whereas single-channel properties of each connexin type are maintained.
我们研究了三种人恶性滋养层细胞(绒毛膜癌)系BeWo、Jeg-3和JAr以及稳定转染大鼠连接蛋白40(Cx40)的Jeg-3细胞中缝隙连接通道的特性。逆转录聚合酶链反应(RT-PCR)、Northern印迹分析和免疫染色显示BeWo和JAr细胞系中有Cx40表达。JAr细胞也表达少量Cx43。RT-PCR显示亲本Jeg-3细胞中Cx40转录本水平极低,但未检测到Cx40蛋白。为了比较内源性和外源性表达的Cx40通道的特性,我们用大鼠Cx40转染了Jeg-3细胞。采用双全细胞法记录来测定各种细胞系和转染细胞中的连接电导(gj)。在Jeg-3细胞中外源性表达的Cx40通道在跨连接电压范围为+/-30至+/-40 mV时表现出陡峭的电压敏感性,单通道主态电导为175 pS,这些值与在BeWo细胞对中内源性表达的Cx40所获得的数据相似。此外,更大的驱动力导致单通道电导仅在BeWo细胞中降低至约30 pS。在JAr细胞对之间,我们测定的gj为10 nS,单通道电导主要为100和152 pS。与Cx40转染细胞和BeWo细胞相比,JAr细胞中的电压依赖性不太敏感。因此,Cx43和Cx40的共表达导致宏观电导具有每种连接蛋白预期特性的混合,而每种连接蛋白类型的单通道特性得以维持。