| |
DOG Congress Home
Invitation
Organization, Deadlines
Overview of the Congress
Scientific Programme
Opening Ceremony
Ceremony 150 Years of DOG
Thursday, 20.September
Friday, 21.September
Saturday, 22.September
Sunday, 23.September
Poster Sessions
Symposia
Courses
Satellite Programme
Information
Social Programme
Sponsors, Exhibitors
DOG Homepage
|
|
AbstractSO.19.09 Loss of Ptf1a gene leads to transdifferentiation of amacrine precursor cells to ganglion cells Sel S.1, Nakhai H.2, Kaliniski T.3, Ehrich D.4, Enssen I.1, Sasse A.1, Vetter E.1, Bräuer L.5, Duncker G. I. W.1, Paulsen F.5 1Klinik und Poliklinik für Augenheilkunde, 5Institut für Anatomie und Zellbiologie, Universität Halle/Wittenberg; 2II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar der Technischen Universität München; 3Institut für Pathologie der Universität Magdeburg; 4Augenklinik Vogtland-Klinikum Plauen Objective: Ptf1a plays a pivotal role for the retinogenesis. In this study we analyse further functions of Ptf1a during the development of the retina. Methods: Using the Cre-loxP-recombination system we have generated a Ptf1aCre/+ mice line and crossed to Z/EG reporter mice line (express GFP-Protein upon excision of a stop codon by Cre) in order to trace the Ptf1a-expressing cells during the development of the mouse retina. Results: We show that the conditional knock-out of Ptf1a leads to transdifferentiation of amacrine precursor cells to ganglion cells. Moreover, we found that Ptf1a is involved in the signalling cascade of cell-cell contacts. Conclusions: These results show that Ptf1a is crucial for the development of amacrine cells during retinogenesis.
|
|