de Smedt H, Eggermont J A, Wuytack F, Parys J B, Van den Bosch L, Missiaen L, Verbis J, Casteels R
Laboratorium voor Fysiologie, Katholieke Universiteit Leuven, Belgium.
J Biol Chem. 1991 Apr 15;266(11):7092-5.
We have studied the expression of the gene 2 for the sarco(endo)plasmic reticulum Ca2+ pump (SERCA2) in BC3H1 cells. Myogenic differentiation not only activated the SERCA2 expression but it also induced an isoform switch. Undifferentiated myoblasts only expressed the SERCA2b isoform (non-muscle) whereas differentiated myocytes predominantly contained the SERCA2a isoform (cardiac/slow skeletal muscle). The isoform switch was documented by immunoblot analysis with isoform-specific antibodies. This observation was confirmed at the mRNA level by using antisense RNA probes specific for class 1 (SERCA2a) or class 2 (SERCA2b) messengers. The expression of the SERCA2a isoform after differentiation was accompanied by a decreased sensitivity of the Ca2+ uptake in permeabilized cells to the Ca2+ pump inhibitor thapsigargin.
我们研究了肌质(内质)网Ca2+泵(SERCA2)基因2在BC3H1细胞中的表达。肌源性分化不仅激活了SERCA2的表达,还诱导了异构体转换。未分化的成肌细胞仅表达SERCA2b异构体(非肌肉型),而分化的肌细胞主要含有SERCA2a异构体(心脏/慢肌型)。通过使用异构体特异性抗体进行免疫印迹分析记录了异构体转换。通过使用针对1类(SERCA2a)或2类(SERCA2b)信使的反义RNA探针,在mRNA水平证实了这一观察结果。分化后SERCA2a异构体的表达伴随着通透细胞中Ca2+摄取对Ca2+泵抑制剂毒胡萝卜素的敏感性降低。