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Experimental Hematology Research topic(s) - Universitäts ...

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<strong>Experimental</strong> <strong>Hematology</strong><br />

<strong>Research</strong> <strong>topic</strong>(s):<br />

1. Hematopoietic Stem Cell Migration<br />

2. Gene Therapy for Patients with Chronic Granulomatous Disease<br />

Group leader(s):<br />

PD Dr. med. Sebastian Brenner<br />

Department of Pediatrics<br />

University Clinic Carl Gustav Carus<br />

Technische Universität Dresden<br />

Fetscherstraße 74<br />

01307 Dresden<br />

Ph: +49-351-458 6833<br />

Fax: +49-351 458 6333<br />

E-mail: Sebastian.Brenner@uniklinikum-dresden.de<br />

Education:<br />

1990 Abitur, Gymnasium Tegernsee, Germany<br />

1990-1997 Medical School: University of Saarland, Homburg/Saar; University<br />

College Dublin, Ireland; Free University Berlin and Humboldt University<br />

to Berlin<br />

1999 Approbation<br />

1999 Dr. med., Humboldt University to Berlin, Germany<br />

2006 Board certified Pediatrician<br />

2008 Board certified Neonatologist<br />

2010 Habilitation (PhD)<br />

Training:<br />

1997-1999 Arzt im Praktikum (Internship), Department of Pediatrics, University<br />

Clinic Dresden (UCD)<br />

1999 Resident, Department of Pediatrics, University Clinic Dresden<br />

1999-2003 Postdoctoral Fellow at the Laboratory of Host Defenses, NIH, USA<br />

2003-2006 Resident, Department of Pediatrics, University Clinic Dresden<br />

since 2008 Senior Physician, Department of Pediatrics, University Clinic Dresden<br />

Clinical Experience:<br />

Experience in general pediatrics, neonatology and pediatric intensive care medicine<br />

Professional Appointment:<br />

Senior Physician at the Department of Pediatrics, University Clinic Dresden<br />

Publications: 27 scientific publications in peer reviewed journals, one patent<br />

Funding: Extrabudgetary funding by DFG, Deutsche Krebshilfe, BMBF<br />

Journals: Reviewer for Blood, Stem Cells, Tissue Engineering and others<br />

Editorial Advisory Board Member of Current Stem Cell <strong>Research</strong> &<br />

Therapy and The Open Tissue Engineering & Regenerative Medicine<br />

Journal<br />

Grant review: DFG, CGD Trust, Swiss National Science Foundation<br />

Societies: Member of Deutsche Gesellschaft für Kinder- und Jugendmedizin,<br />

Gesellschaft für Neonatology und Pädiatrische Intensivmedizin,<br />

European Society of Intensive Care Medicine<br />

Group members:<br />

Scientists: Dr. Sebastian Thieme, Dr. Magdalena Laugsch, Dr. Cornelia Richter,<br />

Dr. Tobias Gyarfas<br />

Technician: Katrin Navratiel


Internal collaborators:<br />

Gerhard Ehninger, Martin Bornhäuser, Department of Internal Medicine I<br />

Dirk Lindemann, Institute of Virology<br />

Dennis Corbeil, Francis Stewart and Konstantinos Anastassiadis, Biotec Center TU Dresden<br />

Frank Buchholz, CBG-MPI Dresden<br />

External collaborators:<br />

Harry L. Malech, LHD, NIAID, NIH, Bethesda, USA<br />

Participation in collaborative research projects (local, national, international):<br />

DFG SFB 655<br />

DFG Center for Regenerative Therapies (CRTD)<br />

List of ten most important publications 2005-2010:<br />

1. Jacobi A, Thieme S, Lehmann R, Ugarte F, Malech HL, Koch S, Thiede C, Müller K, Bornhäuser<br />

M, Ryser M, Brenner S. (2010). Impact of CXCR4 inhibition on FLT3-ITD-positive human AML<br />

blasts. Exp Hematol. Mar;38(3):180-90.<br />

2. Ugarte F, Ryser M, Thieme S, Fierro FA, Navratiel K, Bornhäuser M, Brenner S. (2009). Notch<br />

signaling enhances osteogenic differentiation while inhibiting adipogenesis in primary human<br />

bone marrow stromal cells. Exp Hematol. Jul;37(7):867-875.<br />

3. Ryser MF, Thieme S, Lehmann R, Bornhäuser M, Brenner S. (2009). Serum albumin strongly<br />

influences SDF-1 dependent migration. Int J Hematol. Apr;89(3):269-75.<br />

4. Fierro FA, Brenner S, Oelschlaegel U, Jacobi A, Knoth H, Ehninger G, Illmer T, Bornhäuser M.<br />

(2009) Combining SDF-1/CXCR4 antagonism and chemotherapy in relapsed acute myeloid<br />

leukemia. Leukemia. Feb;23(2):393-6.<br />

5. Moreno-Carranza B, Gentsch M, Stein S, Schambach A, Santilli G, Rudolf E, Ryser MF, Haria S,<br />

Thrasher AJ, Baum C, Brenner S, Grez M. (2009). Transgene optimization significantly improves<br />

SIN vector titers, gp91phox expression and reconstitution of superoxide production in X-CGD<br />

cells. Gene Ther. Jan16(1):111-8.<br />

6. Ryser MF, Ugarte F, Gentsch M, Lehmann R, Bornhäuser M, Brenner S. (2008). S1P1<br />

overexpression stimulates S1P dependent chemotaxis of human hematopoietic stem cells but<br />

strongly inhibits SDF-1/CXCR4 dependent migration and in vivo homing. Mol Immunol.<br />

Nov;46,166-71.<br />

7. Ryser MF, Ugarte F, Thieme S, Gentsch M, Bornhäuser M, Roesen-Wolff A, Brenner S. (2008).<br />

mRNA transfection of a CXCR4-GFP fusion protein - generated by a simple three step PCR<br />

protocol - results in efficient migration of primary mesenchymal stem cells. Tissue Eng Part C<br />

Methods. Sep;14,179-84.<br />

8. Brenner S, Ryser MF, Whiting-Theobald NL, Gentsch M, Linton GF, Malech HL. (2007). The late<br />

dividing population of gamma-retroviral vector transduced human mobilized peripheral blood<br />

progenitor cells contributes most to gene-marked cell engraftment in nonobese diabetic/severe<br />

combined immunodeficient mice. Stem Cells. Jul;25(7):1807-13.<br />

9. Brenner S, Ryser MF, Choi U, Whiting-Theobald N, Kuhlisch E, Linton G, Kang E, Lehmann R,<br />

Rosen-Wolff A, Rudikoff AG, Farese AM, MacVittie TJ, Roesler J, Horwitz ME, Malech HL.<br />

(2006). Polyclonal long-term MFGS-gp91phox marking in rhesus macaques after nonmyeloablative<br />

transplantation with transduced autologous peripheral blood progenitor cells. Mol<br />

Ther. Aug;14(2):202-11.<br />

10. Ueda T, Brenner S, Malech HL, Langemeijer SM, Perl S, Kirby M, Phang OA, Krouse AE,<br />

Donahue RE, Kang EM, Tisdale JF. (2005). Cloning and functional analysis of the rhesus<br />

macaque ABCG2 gene. Forced expression confers an SP phenotype among hematopoietic stem<br />

cell progeny in vivo. J Biol Chem. Jan 14;280(2):991-8.

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