In vivo Disease Model Developing and Applying Laboratory
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Based on our experience in basic research, DML deals with the construction and application of various models of human diseases.
ABOUT US
The In vivo disease model development and service laboratory was established in 2020 within the framework of the National Laboratory of Biotechnology. Our goal is to perform in vivo screenings with molecular libraries and/or labeled molecules on Drosophila models of tumor, neurodegenerative and other nervous system diseases in order to identify new drug candidates. The basis of the laboratory is the 50-year tradition of Drosophila research in Szeged, the 6 currently active research groups and the continuously developed research infrastructure serving them. Relying on the laboratory experience and expertise of our employees, we participate in disease model development projects and provide the opportunity to use the infrastructure as a service.OUR DISEASE MODELS
UNITS OF THE LABORATORY
The molecular biology and biochemical work required for the construction and testing of disease models is carried out in six laboratories specialized for these works.
Insect and mammalian cells are grown, manipulated and tested in the laboratories of the cell and tissue culture unit.
The Drosophila Center consists of laboratories for the work required for genetic manipulations of Drosophila.
The Drosophila Injection Service was established in 2000 at the HUN-REN Biological Research Centre in Szeged. In the 24 years since then, nearly 2,500 transgenic constructs have been injected and around 1,500 transgenic lines have been created.
The Drosophila stock collection of the HUN-REN Szeged Biological Research Centre was founded nearly 50 years ago. Today, it contains more than 10.000 mutant and transgenic lines, most of which are unique in the world. The center includes kitchens that prepare the medium for Drosophila breeding.
The instrument center primarily has fluorescent (confocal, stereo) microscopes and instruments necessary for molecular biological work (PCR, gel documentation, centrifuges).
PARTICIPATING RESEARCH GROUPS
The sarcomeres that make up myofibrils are highly organized contractile structures whose function is closely related to their macromolecular organization. The research group recently developed a nanoscopic method that enabled the localization of muscle proteins with molecular precision. The group also performs the functional characterization of formin-type proteins, in the framework of which it studies the cellular and molecular mechanisms of cytoskeletal regulation.
The research group investigates the physiological and pathological role and mechanisms of autophagy using genetic, cell biological and biochemical methods. In addition to autophagy, the processes of crinophagy (lysosomal degradation of secretory granules) and endocytosis are also studied. In recent years, they have focused on understanding how these various lysosomal degradation processes are coordinated in Drosophila and human cells.
The research group studies the regulation of the transdifferentiation of insect immune cells using a self-developed ex vivo blood cell culturing and differentiation method. During their experiments, they identified factors that play important role in the maintenance of the haematopoietic stem cell niche of the central lymphoid organ and in shaping the fate of differentiating blood cells. Their goal is to discover the functioning of the complex regulatory network that controls the differentiation of blood cells, as well as to reveal the functional and regulatory similarities of the blood cell-forming niches of Drosophila and mammals.
One of the main areas of interest of the research group is the investigation of the biological significance of nuclear actin and the discovery of the mechanisms that ensure its presence in the nucleus. In the last year, the role of nuclear actin in the differentiation of immune cells has also been studied by the group. In addition, the group is also engaged in research into the cellular functions of actin-binding ERM proteins. By creating a mutant with nuclei devoid of ERM protein, the biological significance of the protein's nuclear localization and the problems arising from its absence were determined.
OUR PARTNERS
CONTACT
DML - Disease Modeling Laboratory
6726 Szeged, Temesvári krt. 62.
Working hours
Monday - Friday: 09:00 - 17:00