ZFIN ID: ZDB-LAB-060313-2
Fish Facility of Keio University School of Medicine
PI/Director:
Co-PI / Senior
Researcher:
Makino, Shinji
Contact Person: Makino, Shinji
Email: koshinji@sc.itc.keio.ac.jp
URL:
Address: Department of Regenerative Medicine and Advanced Cardiac Therapeutics 35 Shinanomachi Shinjuku-ku, Tokyo 160-8582, Japan
Country: Japan
Phone: 81-3-5363-3373
Fax: 81-3-5363-3875
Line Designation: None assigned


GENOMIC FEATURES ORIGINATING FROM THIS LAB No data available


STATEMENT OF RESEARCH INTERESTS
Regeneration;
Humans have very limited regenerative capacity. For the most part, when a human tissue or organ is damaged or removed, it is lost forever. The inability to regenerate is shared by many species, including mammals. In humans, this represents a significant medical problem, as the inability to regenerate is the fundamental mechanism underlying many degenerative diseases, including cardiovascular disease, neurodegenerative diseases and aging. Inadequate regenerative capacity is an obvious problem in the setting of acute injury.
By contrast with humans, several organisms have remarkable regenerative abilities. Teleost fish such as zebrafish and urodele amphibians like the newt are two vertebrate organisms that faithfully regenerate many organs and tissues, including skin, bone, joints, nerves, arteries, veins, muscle, limbs (fins), spinal cord, eyes and heart. The secret of their remarkable abilities resides in their genes. The goal of our work is to identify important regeneration genes and use this information to create the molecular and central mechanisms underlying this remarkable phenomenon.


LAB MEMBERS


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
Enomoto, H., Mittal, N., Inomata, T., Arimura, T., Izumi, T., Kimura, A., Fukuda, K., Makino, S. (2020) Dilated Cardiomyopathy (DCM)-linked Heat shock protein Family D Member 1 (HSPD1) mutations cause upregulation of ROS and autophagy through mitochondrial dysfunction. Cardiovascular research. 117(4):1118-1131
Effendi, K., Yamazaki, K., Mori, T., Masugi, Y., Makino, S., and Sakamoto, M. (2013) Involvement of hepatocellular carcinoma biomarker, cyclase-associated protein 2 in zebrafish body development and cancer progression. Experimental cell research. 319(1):35-44
Nishiyama, T., Kaneda, R., Ono, T., Tohyama, S., Hashimoto, H., Endo, J., Tsuruta, H., Yuasa, S., Ieda, M., Makino, S., and Fukuda, K. (2012) miR-142-3p is essential for hematopoiesis and affects cardiac cell fate in zebrafish. Biochemical and Biophysical Research Communications. 425(4):755-761
Shibata, S., Umei, M., Kawahara, H., Yano, M., Makino, S., and Okano, H. (2012) Characterization of the RNA-binding protein Musashi1 in zebrafish. Brain research. 1462:162-173
Lien, C.L., Schebesta, M., Makino, S., Weber, G.J., and Keating, M.T. (2006) Gene Expression Analysis of Zebrafish Heart Regeneration. PLoS Biology. 4(8):e260
Whitehead, G.G., Makino, S., Lien, C.L., and Keating, M.T. (2005) fgf20 is essential for initiating zebrafish fin regeneration. Science (New York, N.Y.). 310(5756):1957-1960
Makino, S., Whitehead, G.G., Lien, C.L., Kim, S., Jhawar, P., Kono, A., Kawata, Y., and Keating, M.T. (2005) Heat-shock protein 60 is required for blastema formation and maintenance during regeneration. Proceedings of the National Academy of Sciences of the United States of America. 102(41):14599-14604