Office Contact Info.
Phone: (631) 344-3604
Fax: (631) 344-2358
Mail address: Bldg. 490
|
 |
Louis A. Peņa
Scientist
Telephone: (631) 344-8041
Lab: (631) 344-8042
Fax: (631) 344-5311
e-mail:
lpena@bnl.gov
|
Research Interests
- Radiation Biology
- Neurobiology/Neuro-oncology
- Growth Factor/Cytokine Receptors
- Radiotracer/PET Probe Development
- Our laboratory investigates cellular and molecular mechanisms of radiation
sensitivity. Ionizing radiation can induce cells to undergo programmed cell
death (apoptosis), independent of DNA damage. Toxic effects are mediated by
stress signal transduction, such as the JNK/SAPK pathway, and antagonized by AKT/PKB
and MAPK/ERK pathways. Our goal is to exploit these pathways develop drugs that protect
normal cells or, conversely, sensitize tumor cells.
- A major focus is on non-neuronal cells of the CNS. This includes normal microvessel
endothelial cells and glial cells such as oligodendrocytes. The former comprise capillaries
and the blood brain barrier, and the latter produce the myelin and white matter of the CNS.
Injury to these cells by therapeutic radiation can result in white matter necrosis and
debilitating neurological deficits in patients. We have demonstrated in cell culture and
in animal models that the heparin-binding cytokine bFGF cuts the level of acute
radiation-induced apoptosis in half in endothelial cells
(Figure 1)
and oligodendrocytes.
- Recently, we have developed a series of synthetic analogs of bFGF. Designated F2A3
and F2A4, these modular, synthetic molecules were shown to stimulate FGF receptors (FGFR1
and FGFR2) in a manner similar to the natural bFGF protein. We are employing them in
models of radiation injury as well as applications for wound healing and tissue regeneration
(press release). For example, a single dose of bFGF,
F2A3, or F2A4 can increase the survival of mice exposed to lethal doses of whole body radiation
(Figure 2).
Further, using the same receptor targeting modules, we are adapting
these synthetic molecules to serve as PET imaging probes to visualize cytokine/growth factor
receptors in vivo. For example, we are employing experimental animal models of Multiple
Sclerosis to create demyelinating lesions in the CNS in which local inflammatory processes
and the breakdown of the blood brain barrier result in an over-expression of cytokine
receptors. We have been able to visualize FGF receptors in these lesions using a conventional
radioisotope
(Figure 3) and will begin to explore positron-emitting isotopes for PET imaging.
Education & Concurrent Positions
- A.B., Harvard University, 1982
- Ph.D., University of California, Los Angeles, 1991
- Postdoctoral Fellow, Cold Spring Harbor Laboratory, 1991-1995
- Research Associate Scientist, Dept. of Radiation Oncology, Memorial
Sloan-Kettering Cancer Center, 1995-99
- Assistant Scientist, Medical Department, BNL, 1999-2001
- Associate Scientist, Medical Department, BNL, 2001-2004
- Scientist, Medical Department, BNL, 2004-present
- Visiting Scholar, Department of Neurobiology & Behavior, Stony
Brook University, 2003-present
- Adjunct Assistant Professor, Department of Biomedical Engineering,
Stony Brook University, 2005-present
- Faculty, Graduate
Program in Neuroscience, State University of New York, Stony
Brook.
Dr. Peņa's Neuroscience Program Webpage
- Faculty, Graduate Program in
Biomedical Engineering, State University of New York, Stony Brook.
Dr. Peņa's BME
Program Webpage
Selected Publications
-
Zhang L.R., Sun W.M., Wang J.J., Zhang M., Yang S.M., Tian Y.P., Vidyasagar S., Pena L.A., Zhang K.Z., et al.
Mitigation effect of an FGF-2 peptide on acute gastrointestinal syndrome after high-dose ionizing radiation.
Int J Radiat Oncol Biol Phys., 77(1);261-268 (2010).
PubMed
-
Lin X., Takahashi K., Campion S.L., Liu Y., Gustavsen G.G., Peņa
L.A. and Zamora P.O.
Synthetic peptide F2A4-K-NS mimics FGF-2 in
vitro and is angiogenic in vivo.
Int. J. Mol. Med., 17(5):833-839 (2006).
PubMed
or Full Text pdf file
-
Lin X., Zamora P.O., Albright S., Glass J.D., and Peņa L.A.
Multidomain synthetic peptide B2A2 synergistically enhances BMP-2
in vitro.
J. Bone Miner Res., 20(4):693-703 (2005).
PubMed
or Full Text pdf file
-
Chen M., Zamora P.O., Som P., Peņa L.A., and Osaki S.
Cell attachment and biocompatibility of polytetrafluoroethylene
(PTFE) treated with glow-discharge plasma of mixed ammonia and oxygen.
J. Biomater Sci. Polym. Ed., 14(9):917-935 (2003).
PubMed
or Full Text pdf file
-
Zamora P.O., Tsang R., Peņa L.A., Osaki S and Som P.
Local delivery of basic fibroblast growth factor (bFGF) using
adsorbed silyl-heparin, benzyl-bis(dimethylsilylmethyl)oxycarbamoyl-heparin.
Bioconjug Chem., 13(5):920-926 (2002).
PubMed or
Full Text pdf file
-
Dilmanian F.A., Button T.M., Le Duc G., Zhong N., Peņa L.A., Smith J.A.,
Martinez S.R., Bacarian T., Tammam J., Ren B., Farmer P.M., Kalef-Ezra
J., Micca P.L., Nawrocky M.M., Niederer J.A., Recksiek F.P., Fuchs A.
and Rosen E.M.
Response of rat intracranial 9L gliosarcoma to microbeam radiation therapy.
Neuro-oncol, 4(1):26-38 (2002).
PubMed
or Full Text pdf file
-
Peņa L.A., Fuks Z. and Kolesnick R.N.
Radiation-induced Apoptosis of Endothelial Cells in the Murine
Central Nervous System:Protection by Fibroblast Growth Factor and
Sphingomyelinase Deficiency.
Cancer Res, 60(2):321-327 (2000).
PubMed
or Full
Text pdf file
-
Separovic D., Pink J.J., Oleinick N.A., Kester M., Boothman D.A.,
McLoughlin M., Peņa L.A. and Haimovitz-Friedman A.
Niemann-Pick human lymphoblasts are resistant to phthalocyanine 4-photodynamic
therapy-induced apoptosis.
Biochem. Biophys. Res. Commun., 258(3):506-512 (1999).
PubMed
or Full Text pdf file
-
Mathias S., Peņa L.A. and Kolesnick R.N.
Signal transduction of stress via ceramide.
Biochem. J., 335( Pt 3):465-480 (1998).
PubMed or
Full Text pdf file
-
Peņa L.A., Fuks Z. and Kolesnick R.N.
Stress-induced apoptosis and the sphingomyelin pathway.
Biochem. Pharmacol., 53(5):615-621 (1997).
PubMed or
Full Text pdf file
-
Santana P., Peņa L.A., Haimovitz-Friedman A., Martin S., Green D., McLaughlin M., Cordon-Cardo C.,
Schuchman E.H., Fuks Z. and Kolesnick R.N.
Acid sphingomyelinase deficient human lymphoblasts and mice are defective in radiation-induced apoptosis.
Cell,86(2):189-199 (1996).
PubMed or
Full
Text pdf file
-
Peņa L.A., Brecher C.W. and Marshak D.R.
b-Amyloid regulates gene expression of glialtrophic substances S100 in C6 glioma and primary astrocyte cultures.
Mol. Brain Res., 34(1):118-126 (1995).
PubMed or
Full Text pdf file
-
Zhong Y. and Peņa L.A.
A novel synaptic transmission mediated by a PACAP-like neuropeptide
in Drosophila.
Neuron, 14(3):527-536(1995).
PubMed or
Full Text pdf file

Last Modified: March 10, 2011 Please forward all questions about this site to:
Denise Monteleone
|