Tokushima University, Japan.
Proc Jpn Acad Ser B Phys Biol Sci. 2010;86(7):707-16. doi: 10.2183/pjab.86.707.
This article summarizes my research over 40 years. The main theme of my work is nitrogen metabolism of amino acids, though later I focused on protein turnover in the cell. In the first years of my research work, I was busy dissecting the pathways involved in the metabolism of certain amino acids and their related enzymes. Then I became interested in the physiology and regulation of matabolism of these amino acids. For that, I used primary cultured hepatocytes, which contain many liver-specific enzymes. However, this play field was very rough around 1970 and hence I had to smooth them (differentiated) first. We discovered a specific growth factor (hepatocyte growth factor, HGF) in rat platelets. Exceptionally, I also worked on branched chain amino acids (valine, leucine and isoleucine). These amino acids are not efficiently metabolized in the liver, so I had to consider the physiology of extrahepatic tissues as well. Finally, I came across a huge protease complex, the proteasome. Whether these players, small amino acid metabolizing enzymes and the huge protease complex, danced well in harmony on my playground or not, I still do not know.
这篇文章总结了我 40 多年的研究工作。我的主要研究主题是氨基酸的氮代谢,但后来我专注于细胞内的蛋白质周转。在我研究工作的最初几年,我忙于剖析某些氨基酸及其相关酶代谢途径。然后,我对这些氨基酸的生理学和代谢调节产生了兴趣。为此,我使用了原代培养的肝细胞,其中含有许多肝脏特异性酶。然而,在 1970 年左右,这个领域非常粗糙,因此我不得不先对其进行细化(分化)。我们在大鼠血小板中发现了一种特定的生长因子(肝细胞生长因子,HGF)。特别的是,我还研究了支链氨基酸(缬氨酸、亮氨酸和异亮氨酸)。这些氨基酸在肝脏中不能有效地代谢,因此我还必须考虑肝外组织的生理学。最后,我遇到了一个巨大的蛋白酶复合物,蛋白酶体。这些参与者,包括小的氨基酸代谢酶和巨大的蛋白酶复合物,是否在我的“游乐场”上和谐共舞,我仍然不得而知。