Sato Tokiharu, Hidaka Kyoko, Iwanaga Asuka, Ito Michihiko, Asano Masahide, Nakabeppu Yusaku, Morisaki Takayuki, Yoshioka Katsuji
Division of Cell Cycle Regulation, Cancer Research Institute, Kanazawa University, 13-1 Takara-machi, Kanazawa, Ishikawa 920-0934, Japan.
Biochem Biophys Res Commun. 2005 Dec 16;338(2):1152-7. doi: 10.1016/j.bbrc.2005.10.052. Epub 2005 Oct 21.
We previously reported that c-Jun NH(2)-terminal kinase (JNK)/stress-activated protein kinase-associated protein 1 (JSAP1), a scaffold protein for JNK signaling, is important in embryonic stem (ES) cells during neurogenesis. In that study, we also observed the altered expression of mesodermal marker genes, which indicated that JSAP1 is involved in the differentiation of mesodermal lineages. Here, we investigated the function of JSAP1 in cardiomyocyte development using JSAP1-null ES cells, and found that cardiomyogenesis was impaired in the JSAP1-null mutant. The JSAP1 deficiency resulted in lower gene expression of the cardiac transcription factor Nkx2.5 and contractile proteins. In contrast, the mutant showed a significantly higher expression of mesoderm-related markers other than those of the cardiomyocyte lineage. Together, these results suggest that JSAP1 may be important for the differentiation of the mesodermal lineages, functioning as a positive factor for cardiomyocyte differentiation, and as an inhibitory factor for differentiation into other lineages.
我们之前报道过,c-Jun氨基末端激酶(JNK)/应激激活蛋白激酶相关蛋白1(JSAP1)作为JNK信号通路的一种支架蛋白,在胚胎干细胞(ES细胞)神经发生过程中具有重要作用。在那项研究中,我们还观察到中胚层标记基因的表达发生了改变,这表明JSAP1参与中胚层谱系的分化。在此,我们利用JSAP1基因敲除的ES细胞研究了JSAP1在心肌细胞发育中的功能,发现JSAP1基因敲除的突变体中,心肌发生受损。JSAP1的缺失导致心脏转录因子Nkx2.5和收缩蛋白的基因表达降低。相反,该突变体显示出除心肌细胞谱系标记物之外的中胚层相关标记物的显著高表达。综上所述,这些结果表明,JSAP1可能对中胚层谱系的分化很重要,作为心肌细胞分化的正向因子以及向其他谱系分化的抑制因子发挥作用。