Stony Brook Hematology

Richard Z. Lin, M.D.
Associate Professor
Departments of Medicine and Physiology & Biophysics
M.D., University of California at San Francisco
Medicine Residency, Stanford University Medical Center
Hematology Fellowship, Stanford University Medical Center
Member: Institute of Molecular Cardiology; Molecular & Cellular Biology Ph.D Graduate Program
Address: HSC T15-045, Stony Brook University, Stony Brook, NY 11794-8151
Phone: 631-444-2059
email: richard.lin@sunysb.edu
Lab Members:
Lisa Ballou (Research
Assistant Professor), Ya-Ping Jiang (Research Scientist), Elzbieta
Selinger (Research Support Specialist), Chia-Yen
Wu (Ph.D. Student), Mohar Chattopadhy (Ph.D. Student), Jun
Yong Choi (Ph.D. Student), Justin Tsai (M.S. Student)
My laboratory's investigation concerns the intracellular
signaling molecules that regulate cell growth. The focus our studies
has been on phosphatidylinositol (PI) 3-kinase that produces the lipid
second messenger, PI(3,4,5)P3. Dysregulation of the PI 3-kinase
signaling pathway is involved in the development of cancer and diabetes
mellitus. Currently, we are using
biochemical and molecular techniques to investigate how the various PI
3-kinase isoforms are regulated. We are also using
genetically modified mice to investigate the physiological consequences
of PI 3-kinase down regulation.
RECENT PUBLICATIONS
1. Ballou LM, Selinger ES, Choi JY, Drueckhammer DG and Lin RZ. Inhibition of Mammalian Target of Rapamycin Signaling by 2-(Morpholin-1-yl)pyrimido[2,1-]isoquinolin-4-one. J. Biol. Chem., epublished June 11, 2007.
2. Said SI, Hamidi SA, Dickman KG, Szema AM, Lyubsky S, Lin RZ,
Jiang Y-P, Chen JJ, Waschek JA and Kort S. Moderate pulmonary arterial
hypertension in male mice lacking the vasoactive intestinal peptide
gene. Circulation, 115:1260-1268, 2007.
3. Jiang Y-P, Ballou LM, Lu Z, Wan L, Kelly DJ, Cohen IS and Lin RZ. Reversible heart failure in Galpha(q) mice. J. Biol. Chem., 281:29988-29992, 2006.
4. Ballou LM, Chattopadhyay M, Li Y, Scarlata, S and Lin RZ. Galpha(q) binds to p110alpha/p85alpha phosphoinositide 3-kinase and displaces Ras. Biochem. J., 394:557-562, 2006.
5. Lu Z, Jiang Y-P, Ballou LM, Cohen IS and Lin RZ. Galpha(q) inhibits
cardiac L-type Ca2+ channels through phosphatidylinositol 3-kinase.
J. Biol. Chem., 280:40347-40354, 2005.
6. Fan G, Jiang Y-P, Lu Z, Martin DW, Kelly DJ, Zuckerman JM, Ballou LM, Cohen IS and
Lin RZ. A transgenic model of heart failure using inducible Galpha(q).
J. Biol. Chem., 280:40337-40346, 2005.
7. Garcia BG, Wei Y, Moron JA, Lin RZ, Javitch JA and Galli A. Akt
is essential for insulin modulation of amphetamine-induced human dopamine
transporter cell-surface redistribution. Mol. Pharmacol., 68:102-109, 2005.
8. Fan G, Ballou LM and Lin RZ. Phospholipase C-independent activation of
glycogen synthase kinase-3beta and C-terminal Src kinase by Galpha(q). J. Biol.
Chem., 278:52432-52436, 2003.
9. Ballou LM, Jiang Y-P, Du G, Frohman MA and Lin RZ. Ca2+-
and phospholipase D-dependent and -independent pathways activate mTOR
signaling. FEBS Lett., 550:51-56, 2003.
10. Ballou LM, Lin H-Y, Fan G, Jiang Y-P and Lin RZ. Activated
Galpha(q) inhibits p110alpha phosphatidylinositol 3-kinase and Akt. J. Biol
. Chem., 278:23472-23479, 2003.
11. Lin H-Y, Ballou LM and Lin RZ. Stimulation of the alpha1A
adrenergic receptor inhibits PDGF-induced PDGF receptor Tyr751 phosphorylation
and PI 3-kinase activation. FEBS Lett., 540:106-110, 2003.