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Structure <strong>of</strong> <strong>the</strong> Group<br />

Group Leader<br />

Pr<strong>of</strong>. Dr. Helmut Kettenmann<br />

Assistant to <strong>the</strong><br />

Group Leader<br />

Meino Gibson<br />

Scientists<br />

Dr. Rainer Glass<br />

Dr. Katrin Faerber<br />

Dr. Christiane Nolte<br />

(part-time)<br />

Dr. Daniel Reyes-Haro<br />

Dr. Brigitte Haas<br />

Dr. Darko Markovic<br />

Graduate Students<br />

Bruno Benedetti<br />

Giselle Cheung<br />

Sridhar Chirasani<br />

Jitender Kumar<br />

Jochen Müller<br />

Marta Maglione<br />

Stefanie Seifert<br />

Technical Assistants<br />

Rainer Kröber<br />

(for <strong>the</strong> department)<br />

Brigitte Gerlach (part-time)<br />

Irene Haupt<br />

Karin Heufelder<br />

Michaela Seeger-Zografakis<br />

(part-time)<br />

Secretariat<br />

Birgit Jarchow<br />

Figure 3. Neural Stem cells accumulate at gliomas<br />

Glioma cells were injected into <strong>the</strong> brain <strong>of</strong> a mouse and formed a<br />

tumor. The glioma cells can be recognized by <strong>the</strong>ir permanent red<br />

label. Nestin-positive stem cells can be recognized by <strong>the</strong>ir green<br />

colour since we used a transgenic mouse line with nestin-promoter<br />

driven expression <strong>of</strong> <strong>the</strong> green fluorescent protein. The stem cells can<br />

be recognized at <strong>the</strong>ir normal location, <strong>the</strong> subventricular zone and<br />

associated with <strong>the</strong> red tumor cells.<br />

Do stem cells influence glioma cells?<br />

We recently observed that gliomas attract neural precursor<br />

cells from <strong>the</strong> germinal zone. These cells migrate over large<br />

distances and enwrap <strong>the</strong> tumor yet <strong>the</strong>y do not originate<br />

from <strong>the</strong> tumor proper as was previously suspected. This<br />

intrinsic anti-tumorigenic response is strongly related to<br />

age in an animal model and occurs only during youth when<br />

neural precursor cells are more active. Consequently, in<br />

older animals this interaction does not occur. The precursor<br />

cells inhibit tumor growth and addition <strong>of</strong> exogenous precursors<br />

prolongs <strong>the</strong> survival rate in older animals. We are<br />

now interested in <strong>the</strong> factors by which glioma cells attract<br />

<strong>the</strong> stem cells to <strong>the</strong> tumor and in <strong>the</strong> factors by which stem<br />

cells influence glioma growth. We have <strong>the</strong>refore developed<br />

in vitro assays (funded by Helmholtz-Ideenwettbewerb).<br />

Selected Publications<br />

Glass R, Synowitz M, Kronenberg G, Markovic D, Wang LP, Gast<br />

D, Kiwit J, Kempermann G and Kettenmann, H. (2005). Gliomainduced<br />

attraction <strong>of</strong> endogenous neural precursor cells is associated<br />

with improved survival, J. Neurosci., 25, 2637-2646.<br />

Heidemann A C, Schipke C G, Kettenmann H. (2005)<br />

Extracellular application <strong>of</strong> nicotinic Acid adenine dinucleotide<br />

phosphate induces Ca 2+ signaling in astrocytes in situ, J. Biol.<br />

Chem., 280, 35630-35640.<br />

Haas B, Schipke C G, Peters O, Söhl G, Willecke K. and<br />

Kettenmann H. (2006) Activity-dependent ATP-waves in <strong>the</strong><br />

Mouse Neocortex are Independent from Astrocytic Calcium<br />

Waves. Cereb Cortex, 16, 237-46.<br />

Synowitz M, Glass R, Faerber K, Markovic D, Kronenberg G,<br />

Herrmann K, Schnermann J, Nolte C, van Rooijen N, Kiwit J, and<br />

Kettenmann H. (2006) A1 Adenosine Receptors in Microglia<br />

Control Glioblastoma-Host Interaction. Cancer Res 66,<br />

8550-8557.<br />

Hanisch U-K and Kettenmann K (2007) Microglia – active sensor<br />

and versatile effector cells in <strong>the</strong> normal and pathologic brain,<br />

Nature Neuroscience, 10,1387-1394.<br />

Pocock, J M and Kettenmann H. (2007) Neurotransmitter<br />

receptors on microglia, Trends Neurosci., 30, 527-535.<br />

Function and Dysfunction <strong>of</strong> <strong>the</strong> Nervous System 163

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