
Register now to: Keisen Nadia Liss
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2. Shootin 1 - Novel Proteins for neuronal network
formation in brain by Assoc. Prof. N. Inagaki
http://bsw3.naist.jp/itoh/home/index.html
In a brain, neurons work as if they were semi-conductors
constituting a computer. For these to function, the
polarity of neurons is important. How does the neuron
form the axon and dendrite to acquire polarity? We have
attempted to clarify this issue at the molecular level by
means of proteome analysis and found a novel protein
named Shootin1, which regulates the polarity of axon.
This finding will lead to the therapy of neuro-degenerating
disease such as Head Injury and Neuropathy.

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3. Neuropsin - Novel serine-protease, a role in the
mechanism for learning and memory by Prof. S.
Shiosaka (tentative)
http://bsw3.naist.jp/shiosaka/siosaka.html
Our research is focused on the neural functions of
cerebral cortex and limbic brain (hippocampus, amygdala,
etc.) using techniques of neuroanatomy, electrophysiology,
biochemistry and behavioral neuroscience. One of major
topics is the elucidation of a mechanism for learning and
memory. To date, we have demonstrated that neuropsin
(klk8) plays a significant role in the regulation of E-LTP
(early phase of long-term potentiation), and regulates
intracellular signals of the limbic brain. We expect the
study results contribute to the therapy of CNS disease
such as Alzheimer disease.

4. Osteoclast differentiation and bone metabolism -
osteoporosis and autoimmune diseases by Prof.
T. Takeya
http://bsw3.naist.jp/takeya/takeya.html
Osteoclasts, involved in bone resorption, play a central
role in bone metabolism. Disturbed formation of
osteoclasts can lead to the diseases such as
osteoporosis and Rheumatoid Arthritis. We are
placing an emphasis on the analysis of the function
of NFAT2, a key differentiation regulator; the
mechanism for cell fusion seen during differentiation
and the mechanism for intracellular signal
transduction involving proto-oncogene Src.
Interesting finding in our research could lead to the
novel therapy of bone disease and autoimmune
disease.
Osteoclast Differentiation Process

5 a. Connection between cell cycle progression
and oncogenesis (Prof. Jun-ya Kato)
http://bsw3.naist.jp/kato/kato.html
Prof. Kato focuses on the molecular mechanisms
controlling proliferation, differentiation, and death
of mammalian cells, and studies the connection
between cell cycle progression and oncogenesis,
as well as differentiation, proliferation, and
leukemogenesis in hematopoietic cells. The
findings can be applied to regenerative medicine
and cancer research. Especially he is investigating
the molecular mechanisms underlying
leukemogenesis, focusing on AML (acute myeloid
leukemia), MDS (myelodysplastic syndromes), and
CML (chronic myeloid leukemia).

5 b. Unique Mouse models of hepatitis and
diabetes mellitius (Prof. Kenji Kohno)
http://bsw3.naist.jp/kouno/kouno.html
Prof. Kohno, using a unique TRECK method, has
created mouse models of hepatitis and diabetes
mellitus. These TRECK-Tg mice will be useful not
only in developing new therapies but also in
exploring tissue-stem cells of adult mice. He is
attempting to apply these mouse models to
regenerative medicine (isolation and identification
of hepatic stem cells and pancreatic beta-stem
cells).

5 c. Research on genes regulating TGF-β
signals and its application to RA and OA
(Dr. Chiyo Oka)
http://bsw3.naist.jp/kawaichi/kawaiti.html
TGF-β is dispensable for shaping of animals,
e.g., for determination of the dorsoventral axis of
early embryos and regulation of the
differentiation of fetal skeleton. It is also involved
in preservation of the function of various organs
of mature organisms. Its abnormalities can lead
to malignant courses of tumors and onset of
common sicknesses such as pulmonary fibrosis
and osteoarthritis. Prof Kawaichi and Dr. Oka
have identified a previously unknown gene HtrA1
involved in the formation of bone and joint, onset
of arthritis, tumor malignancy and so on; and are
analyzing its physiological functions. These
researches could lead to the therapy of TGF-β
related diseases such as OA, RA and cancer.
