logomark
Research

Research

BDR researchers coming from diverse research fields are working together to achieve higher goals.

Seminars & Symposia

Seminars & Symposia

BDR hosts annual symposium and regular seminars inviting international scientists in life science.

Careers & Study

Careers & Study

BDR embraces people from diverse backgrounds, and strives to create an open and supportive setting for research.

Outreach

Outreach

BDR communicates the appeal and significance of our research to society through the use of various media and activities.

News

News

From research, events, people and everything in between, find out what’s going on at RIKEN BDR.

About Us

About Us

Exploring the scientific foundations of life through interdisciplinary approaches to address society’s problems.

principal investigator

Team Director
Satoko Arakawa Ph.D.

Laboratory for Ultrastructural Research

LocationKobe / Developmental Biology Buildings

E-mailarako@riken.jp

Elucidating how changes in intracellular structure manifest as functional changes in living tissues

The Laboratory for Ultrastructural Research aims to elucidate the relationship between cellular structure and function, using electron microscopy–based ultrastructural analysis as a central approach. Intracellular architecture changes dynamically in response to genetic variation, cell–cell interactions, and environmental cues, and its disruption can lead to functional abnormalities and pathophysiological states in living tissues.

We seek to understand how structural changes shape cellular and tissue function through studies of morphological transitions during differentiation, the physiological role of Golgi membrane-associated degradation (GOMED), and previously uncharacterized forms of cell death in tissues.

Selected Publications

Nibe-Shirakihara Y, Honda S, Arakawa S, et al.
Optineurin is an adaptor protein for ubiquitinated substrates in Golgi membrane-associated degradation.
Nature Communications 16, 8966 (2025) doi: 10.1038/s41467-025-64400-3

Yamaguchi H, Honda S, Torii S, et al.
Wipi3 is essential for alternative autophagy and its loss causes neurodegeneration
Nature Communications 11, 5311 (2020) doi: 10.1038/s41467-020-18892-w

Torii S, Yamaguchi H, Nakanishi A, et al.
Identification of a phosphorylation site on Ulk1 required for genotoxic stress-induced alternative autophagy
Nature Communications 11, 1754 (2020) doi: 10.1038/s41467-020-15577-2

Arakawa S, Tsujioka M, Yoshida T, et al.
Role of Atg5-dependent cell death in the embryonic development of Bax/Bak double-knockout mice
Cell Death & Differentiation 24(9), 1598-1608 (2017) doi: 10.1038/cdd.2017.84

Watanabe Y, Honda S, Konishi A, et al.
Autophagy controls centrosome number by degrading Cep63
Nature Communications 7, 13508 (2016) doi: 10.1038/ncomms13508

Yamaguchi H, Arakawa S, Kanaseki T, et al.
Golgi membrane-associated degradation pathway in yeast and mammals
The EMBO Journal 35(18), 1991-2007 (2016) doi: 10.15252/embj.201593191

Honda S, Arakawa S, Nishida Y, et al.
Ulk1-mediated Atg5-independent macroautophagy mediates elimination of mitochondria from embryonic reticulocytes
Nature Communications 5, 4004 (2014) doi: 10.1038/ncomms5004

Narita M, Young A, Arakawa S, et al.
Spatial Coupling of mTOR and Autophagy Augments Secretory Phenotypes
Science 332(6032), 966-970 (2011) doi: 10.1126/science.1205407

Nishida Y, Arakawa S, Fujitani K, et al.
Discovery of Atg5/Atg7-independent alternative macroautophagy
Nature 461(7264), 654-658 (2009) doi: 10.1038/nature08455

Shimizu S, Kanaseki T, Mizushima N, et al.
Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes
Nature Cell Biology 6(12), 1221-1228 (2004) doi: 10.1038/ncb1192

PAGE
TOP