FORIPS
BAVARIAN RESEARCH NETWORK INDUCED PLURIPOTENT STEM CELLS
The association
Neurological and psychiatric disorders such as Parkinson's disease (PD) pose significant therapeutic, social and health-economic challenges to society. Affected individuals are often severely impaired, experiencing far-reaching personal and social sequalae. Novel and improved treatment options are urgently needed to help these patients.
Researchers hope for new insights into the pathogenesis as well as new treatment approaches using patient specific disease models based on the "induced pluripotent stem cells" technology (iPS).
Reprogramming of mature cells of the body into so called “induced pluripotent stem cells“ represents one of the most innovative biomedical developments of recent years (Nobel Prize in Medicine 2012 for Shinya Yamanaka and John B Gurdon). Using this technology, connective tissue cells of the patients can be re-programmed to the stage of pluripotency. As a result, patient-specific stem cells are generated and can be further differentiated into organ-specific cells. These cells may serve as a cellular model for the analysis of specific or individual disease causes, thus enabling the development of new treatment strategies.
ForIPS aims to establish the iPS technology and to use the iPS cell derived neural cells as cellular models to analyze the pathogenesis of PD. Scientists at ForIPS re-program skin cells from PD patients and healthy control subjects, and differentiate those patient specific iPS cells into neural cells. As these neural cells constitute very specific cellular models researchers hope to decipher the underlying pathogenic mechanisms of PD.
In addition, the research groups at ForIPS will establish a biobank for human iPS cells and will implement the iPS technology at all associated Bavarian universities. With this, an efficient platform for advanced investigation of other brain diseases and disorders of other organs will be created.
Sporadic Parkinson’s disease (PD)
ForIPS focusses on sporadic PD, with over 85 percent the most common form of all Parkinson syndromes. After Alzheimer's disease, PD is the second most common neurodegenerative disease worldwide, and causes in the brains of affected patients a profound loss of neurons that control motor functions, causing symptoms like an overall slowing of movements (bradykinesia), increased muscle tone (rigor), and tremor. Beside motor functions, also non-motor functions such as hyposmia, sleep disorders and depression are frequently observed prior to the onset of motor deficits. Current therapeutic approaches are hardly able to halt or even reverse the progression of the disease. In addition, the etiology of sporadic PD is multifactorial, and moreover, the underlying molecular and cellular mechanisms of each affected individual remain largely unknown. The monogenic forms of PD and the analysis of PD models up to date indicate that alterations of important intracellular functions play a role in the pathogenesis of PD. In order to define new targets for therapeutic strategies it is essential to use PD patient derived cells to decipher individual disease mechanisms.
Network:
In the Bavarian Research Network ForIPs collaborate 15 project groups from the following Bavarian Universities:
Friedrich-Alexander-University Erlangen-Nuremberg (FAU)
Ludwig-Maximilians-Universität of Munich (LMU)
Technische Universität München (TU)
University of Regensburg
Julius-Maximilians-University of Wuerzburg
Institut Technik, Theologie, Naturwissenschaften (TTN) an der LMU München
Organisation
Spokesperson
Second Spokesperson
General Management
Head of Research Division
- Prof. Dr. Benedikt Berninger
- Prof. Dr. Johann Helmut Brandstätter
- Prof. Dr. Peter Dabrock
- Prof. Dr. Frank Edenhofer
- Prof. Dr. Günter U. Hoeglinger
- Dr. Marisa Karow
- PD Dr. Jochen Klucken
- Dr. Zacharias Kohl
- Prof. Dr. Chichung Dieter Lie
- PD Dr. theol. Habil. Arne Manzeschke
- Dr. Iryna Prots
- Prof. Dr. Markus Riemenschneider
- Dr. Sigrid Schwarz
- Prof. Dr. Michael Sendtner
- Dr. Daniela Vogt
- Prof. Dr. Michael Wegner
- PD Dr. Beate Winner
- Prof. Dr. Wolfgang Wurst
Scientist
Secretary
Technician
Partner
Fields of work
Projects
- Accompanying research on bioethical aspects and the discourse with the general public
- Establishment of a biobank for iPs cell and derived neural cell lines
- Genetic and epigenetic characterization of the cells
- Testing new therapeutic strategies
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Investigation of biological alterations and functional deficits in neural and glial cells
- Analysis of neurites and chemical synapses in Parkinson patients derived iPS cells and neurons
- Modelling astropathy for idiopathic Parkinson disease – an approach using induced pluripotent stem cell differentiation
- Generation and validation of induced pluripotent stem cells for modeling of motor neuron diseases
- Human in-vitro model for the neuroinflammation in the idiopathic Parkinson Syndrom
- Microtubule-associated Protein Tau as a Pathogenic Factor of Idiopathic Parkinson’s Syndrome (IPS)
- Mitochondrial function in induced pluripotent stem cells (iPS) and thereof derived dopaminergic neurons of patients with Parkinson´s Disease
- Analysis of aging-dependent cellular processes in Parkinson syndrome using novel reprogramming strategies
- Role of autophagy-associated processes in the pathophysiology of PD
News
Events
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27.10.2016
Meeting ForIPS
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19.02.2016
Meeting ForIPS
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18.02.2016
Seminar Animal Ethics
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24.10.2015
Lange Nacht der Wissenschaften Nürnberg Erlangen
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03.07.2015
Internationale Symposium ForIPS
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29.06.2015
Wolfgang Hillen Summer School 2015, Translational Challenges for Neurodegenerative and -psychiatric Disorders: From Models to Patients.
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20.02.2015
Meeting of ForIPS February 2015
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24.11.2014
Bioethics in Discourse: Playing God
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09.11.2014
BaCaTeC Graduate School - Translational challenges for Neurodegenerative and -psychiatric disorders: From models to patients
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29.09.2014
Meeting ForIPS September 2014
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24.04.2014
ForIPS seminar
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30.01.2014
Workshop Basic Stem Cell Skills
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10.10.2013
Kick-off Meeting ForIPS
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Contact
Dr. Rosi Lederer
Mobile: +49 173 4828542
rosi.lederer@med.uni-muenchen.de
Physiologisches Institut Lehrstuhl für Physiologische Genomik
Pettenkoferstr.12
80336 München
Jasmin Burczyk
Tel: +49 9131 8539324
jasmin.burczyk@uk-erlangen.de
Universitätsklinikum Erlangen Abteilung für Molekulare Neurologie
Schwabachanlage 6
91054 Erlangen