Antimicrobial Agents

The goal of this unit is the development of a preventative and at least partially curative gene therapy for arthrosclerosis. Using vascular models, genes and promoters are identified that can be activated by biomechanical forces such as flow or stretching. Because cardiovascular disease is often induced by dental disease (caries, periodontitis), a second focus of the unit is in the establishment of a therapy against oral streptococcus.

Application of antimicrobial peptides for increasing the shelf life of food products

The effect of antimicro­bial peptides on the growth of Candida albicans.
© Photo Fraunhofer IZI

The effect of antimicro­bial peptides on the growth of Candida albicans.

Antimicrobial peptides (AMP) are an integral component of the defense systems of animals and plants. Their range of activity comprises bacteria, fungi and viruses. The intended project aims at the development of suitable peptides that effectively kill germs, in particular those associated with putrefaction, during production processes in the food industry. Thereby, for instance, the shelf life of fresh salads is intended to be increased by at least two days. On the basis of preliminary studies, sequence motifs have been produced from AMP having a known antimycotic / antibacterial activity and their effectiveness against yeasts, mildew and enterococci has been tested in an in vitro assay. We plan to concentrate, in particular, on short-chain antimicrobial peptides (<20 amino acids) as there are no immunological complications to be expected in case of a later application in association with food products. Five AMP could be identified that have a potent inhibitory effect on the growth of fungi and bacteria. No measurable toxicity to eukaryotic cells could be observed.

Development of therapeutically effective peptides for the treatment of contagious and tumor diseases

The need for new, effective drugs based on bioactive substances has increased greatly in recent years. The predictions for the future also reveal strong growth in this segment. This trend was picked up on in the Vascular Biology Unit and a technology platform was created which is able to develop and evaluate peptides both against multi-resistant hospital germs and also against tumor cells. This DNA-based technology allows an appropriate, antibiotically effective peptide to be developed against every relevant hospital germ by means of a high-throughput technique. Some of these antimicrobial peptides have a broad-spectrum effect and could thus be applied against a number of different types of bacteria or also pathogenic fungi (e.g. candida albicans).

During the course of 2012, several sequence libraries were established with partly differing ranges of efficacy, e.g. against human-pathogenic oral germs (cariogenic germs such as streptococcus mutans, streptococcus sobrinus or pathogens associated with paradontitis such as actinobacillus actinomycetemcomitans, porphyromonas gingivalis), germs found in the gastrointestinal tract (heliobacter pylori) and also against germs found in the respiratory tract (haemophilus influenzae).

The use of bioactive substances from plants, insects and amphibians for the treatment of inflammations and also tumor diseases (e.g. the so-called ”frog vaccine”) has been common practice for a number of years, particularly among the indigenous peoples of Central and South America. This is why, together with the Immunotherapy – Oncology Unit, peptides from the skin secretion of tropical frog species (e.g. phyllomedusa bicolor) were cloned in an additional experimental approach and several amino acids from these peptides were mutated at defined positions. Compared with the original peptides, it could be demonstrated in vitro that the cytotoxicity of these peptides, in comparison with tumor cells, could be increased by modifying the amino acid sequence, while control cells showed a comparably high level of resistance. Although the mechanism of action of these peptides was not yet able to be clarified, the assumption suggests that the different composition and net charge of the cell membrane of tumor cells and non-tumor cells play a decisive role here. Moreover, some of these peptides may have an additional, immunomodulatory effect.

Development of tumor therapeutics and antibiotics from plant extracts

Bark of an African plant from which ingredients were isolated.
© Photo Fraunhofer IZI

Bark of an African plant from which ingredients were isolated.

About 80 percent of the tumor therapeutics currently in use originate from substances of the secondary plant metabolism. Many tumor diseases (e. g. brain tumors, pancreatic carcinoma) are still difficult or even impossible to cure despite the progress that has been made in developing new chemotherapeutic agents. In close cooperation with naturopathic scientists from Africa substances / extracts from about 20 plant species were prepared which, to some extent, have a potential as new anti-tumor drugs for a potential application in palliative care. First examinations on various cancer cell lines attest the selective effect of the plant ingredients on tumor cells. These data could be verified in experiments in a mouse model. This gives rise to new options for tumor therapy, in particular for brain tumors. Moreover, some plants hold highly effective antibiotic ingredients, in particular in bark and roots, which also have the potential for applications in human medicine.

Development of silicon surfaces for the directed differentiation of murine stem cells

Cultivation of murine stem cells on microstructured silicon surfaces with the aim of induc­ing directed differentiation.
© Photo Fraunhofer IZI

Cultivation of murine stem cells on microstructured silicon surfaces with the aim of induc­ing directed differentiation.

In most cases, stem cells are located in tissue niches and exhibit a low metabolic activity. Their differentiation is only initiated by altered conditions (stimuli) in the microenvironment. The exact sequence of processes, however, is mostly unknown. Stem cell differentiation is significantly determined by intrinsic cellular signaling and extrinsic stimulators (cell-to-cell contact, contact between cell and extracellular matrix). Extrinsic signaling can be of a chemical (e.g. growth factors and cytokines) and also of a mechanical (expansion forces acting on cells due to interactions with micro- or nanostructured surfaces) nature. In the present project, a cell culture matrix prototype with a nanostructured surface (e.g. covalent peptide binding on cell culture basis, mechanical structuring patterns) shall be developed which is capable of inducing the differentiation behavior of stem cells in a directed manner.

  • CREAVAC-Creative Vakuumbeschichtung GmbH
  • DMG Chemisch-Pharmazeutische Fabrik GmbH
  • Geräte- und Vorrichtungsbau Spitzner OHG
  • Heart Center Leipzig
  • Höft, Wessel & Dr. Dreßler GmbH
  • KET Kunststoff- und Elasttechnik GmbH
  • Leibniz Institute of Surface Modification
  • Medichema GmbH
  • ÖHMI Analytik GmbH
  • Pilot Pflanzöltechnologie Magdeburg e.V.
  • Saarland University Hospital and Saarland University Faculty of Medicine
  • Saarland University Medical Center, Clinic for Tooth Preservation, Parodontology and Preventive Dentistry

  • Oelkrug C, Lange CM, Wenzel E, Fricke S, Hartke M, Simasi J, Schubert A. Analysis of the tumoricidal and anti-cachectic potential of curcumin. Anticancer Research. 2014 Sep;34(9):4781-8.
  • Simasi J, Oelkrug C, Schubert A, Nieber K, Gillissen A. The role of BIM-EL and BCL2-α on the efficacy of erlotinib and gefitinib in lung cancer. Respiratory Physiology and Neurobioly. 2014 Oct 6. pii: S1569-9048(14):259-6. DOI: dx.doi.org/10.1016/j.resp.2014.09.022.
  • Simasi J, Schubert A, Oelkrug C, Gillissen A, Nieber K. Primary and secondary resistance to tyrosine kinase inhibitors in lung cancer. Anticancer Research. 2014 Jun;34(6):2841-50.
  • Rupf S, Idlibi AN, Marrawi FA, Hannig M, Schubert A, von Mueller L, Spitzer W, Holtmann H, Lehmann A, Rueppell A, Schindler A. Removing biofilms from microstructured titanium ex vivo: a novel approach using atmospheric plasma technology. PLoS One.6 (2011), 10, e25893, 9 S. DOI dx.doi.org/10.1371/journal.pone.0025893
  • Rupf S, Lehmann A, Hannig M, Schafer B, Schubert A, Feldmann U, Schindler A. Killing of adherent microbes by a non-thermal atmospheric plasma jet. J Med Microbiol. 59 (2010), Pt 2, S. 206-12.
  • Aupperle H, Thielebein J, Kiefer B, März I, Dinges G, Schoon HA, Schubert A. Expression of genes encoding matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in normal and diseased canine mitral valves. J Comp Pathol, 140 (2009), 4, S. 271-277.
  • Sommer G, Kralisch S, Stangl V, Vietzke A, Köhler U, Stepan H, Faber R, Schubert A, Lössner U, Bluher M, Stumvoll M, Fasshauer M. Secretory products from human adipocytes stimulate proinflammatory cytokine secretion from human endothelial cells. J Cell Biochem, 106 (2009), 4, S. 729-37.
  • Aupperle H, März I, Schubert A, Dinges G, Thielebein J, Schoon HA. Störungen des Metabolismus der extrazellularmatrix des Herzens bei der kaninen idiopathischen dilatativen Kardiomyopathie. Der praktische Tierarzt 89 (2008), 12, S. 998-1005.
  • Goettsch W, Schubert A, Morawietz H. Expression of human endothelinconverting enzyme isoforms: role of angiotensin II. Can J Physiol Pharm 86 (2008), 6, S. 299-309.
  • Haussig S, Schubert A, Mohr FW, Dhein S. Sub-chronic nicotine exposure induces intercellular communication failure and differential down-regulation of connexins in cultured human endothelial cells. Atherosclerosis 196 (2008), 1, S. 210-8.
  • Kralisch S, Sommer G, Stangl V, Köhler U, Kratzsch J, Stepan H, Faber R, Schubert A, Lössner U, Vietzke A, Bluher M, Stumvoll M, Fasshauer M. Secretory products from human adipocytes impair endothelial function via nuclear factor kappaB. Atherosclerosis 196 (2008), 2, S. 523-31.
  • Pfefferkorn P, Scholz U, Veneruso V, Nikolaus T, Madin K, Eichenlaub U, Schubert A, Lehmann J. Influence of Serum Deprivation on Adherence and Proliferation of Murine Mesenchymal Progenitor Cells Analysed with Roche´s xCELLigence System. Biochemica (2008), 4, S. 14-16.
  • Aupperle H, Garbade J, Schubert A, Barten M, Dhein S, Schoon HA, Mohr FW. Effects of autologous stem cells on immunohistochemical patterns and gene expression of metalloproteinases and their tissue inhibitors in doxorubicin cardiomyopathy in a rabbit model. Vet Pathol 44 (2007), 4, S. 494-503.
  • Morawietz H, Erbs S, Holtz J, Schubert A, Krekler M, Goettsch W, Kuss O, Adams V, Lenk K, Mohr FW, Schuler G, Hambrecht R. Endothelial protection, AT1 blockade and cholesterol-dependent oxidative stress: the EPAS trial. Circulation, 114 (2006), 1, S. 1296-1301.
  • Walther T, Schubert A, Wustmann T, Falk V, Walther C, Doll N, Rastan A, Gummert J, Mohr FW. Reverse remodeling of cardiac collagen protein expression after surgical therapy for experimental aortic stenosis. J Heart Valve Dis, 15 (2006), 5, S. 651-6.
  • Garbade J, Schubert A, Rastan AJ, Lenz D, Walther T, Gummert JF, Dhein S, Mohr FW. Fusion of bone marrow-derived stem cells with cardiomyocytes in a heterologous in vitro model. Eur J Cardio-Thorac, 28 (2005), 5, S. 685-91.
  • Gielen S, Adams V, Linke A, Erbs S, Mobius-Winkler S, Schubert A, Schuler G, Hambrecht R. Exercise training in chronic heart failure: correlation between reduced local inflammation and improved oxidative capacity in the skeletal muscle. Eur J Cardiov Prev R,12 (2005), 4, S. 393-400.
  • Hambrecht R, Schulze PC, Gielen S, Linke A, Mobius-Winkler S, Erbs S, Kratzsch J, Schubert A, Adams V, Schuler G. Effects of exercise training on insulin-like growth factor-I expression in the skeletal muscle of non-cachectic patients with chronic heart failure. Eur J Cardiov Prev R,12 (2005), 4, S. 401-6.
  • Linke A, Adams V, Schulze PC, Erbs S, Gielen S, Fiehn E, Mobius-Winkler S, Schubert A, Schuler G, Hambrecht R. Antioxidative effects of exercise training in patients with chronic heart failure. Increase in radical scavenger enzyme activity in skeletal muscle. Circulation, 111 (2005), 14, S. 1763-70.
  • Rastan AJ, Walther T, Kostelka M, Garbade J, Schubert A, Stein A, Dhein S, Mohr FW. Morphological, electrophysiological and coupling characteristics of bone marrow-derived mononuclear cells-an in vitro-model. Eur J Cardio-Thorac, 27 (2005), 1, S. 104-10.