Capiati D A, Vazquez G, Tellez Iñón M T, Boland R L
Departamento de Biología, Bioquímica y Farmacia, Universidad Nacional del Sur, San Juan, Bahía Blanca, Argentina.
Cell Prolif. 2000 Oct;33(5):307-15. doi: 10.1046/j.1365-2184.2000.00182.x.
Protein kinase C (PKC) has been implicated in the control of proliferation and differentiation of many cell types. There is evidence indicating that it plays a role in signal transduction mechanisms related to myogenesis, but little is known about the individual functions of PKC isoforms in muscle cell development. Data obtained in previous studies using cultured chick embryo skeletal muscle cells suggested that PKC alpha is linked to the regulation of myoblast proliferation. However, this causal relationship could not be definitively established as no experiments based on selective inhibition of this isoform were carried out. In the present work, specific inhibition of the expression of PKC alpha in cultured myoblasts by using antisense oligonucleotide technology resulted in a significant decrease of culture cell density and DNA synthesis, clearly showing that this isoenzyme is involved in signalling pathways which promote muscle cell proliferation.
蛋白激酶C(PKC)与多种细胞类型的增殖和分化调控有关。有证据表明它在与肌生成相关的信号转导机制中发挥作用,但对于PKC同工型在肌肉细胞发育中的具体功能了解甚少。先前使用培养的鸡胚骨骼肌细胞进行的研究数据表明,PKCα与成肌细胞增殖的调节有关。然而,由于没有进行基于选择性抑制该同工型的实验,这种因果关系无法明确确立。在本研究中,通过使用反义寡核苷酸技术特异性抑制培养的成肌细胞中PKCα的表达,导致培养细胞密度和DNA合成显著降低,清楚地表明这种同工酶参与促进肌肉细胞增殖的信号通路。