Prof. Dr. Anna von Mikecz

Research Interest

Alzheimer's, Parkinson's and a family of poly-glutamine(Q) expansion diseases are defined by amyloid-like protein fibrillation and neurodegeneration. We are particularly interested in the interactions between the fibrillogenesis of endogenous polyQ-proteins in the cell nucleus and gene expression. As formation of poly-Q-containing amyloid is preceded by a series of protein fibrillation steps, these steps are characterized in correlation to nuclear function and respective genetic modifiers. Our research is based upon the idea that comprehension of the physiological role of polyQ repeats is a prerequisite to uncover the underlying mechanisms of aberrant protein fibrillation and neurodegenerative aggregation diseases.

Specific Projects

Intranuclear inclusions as proteolytic centers

We have shown in cell culture systems that xenobiotics such as nanoparticles and heavy metals alter the protein homeostasis in the cell nucleus and induce aberrant fibrillation of proteins to amyloid-like intranuclear inclusions. These inclusions contain components of the ubiquitin-proteasome system (UPS) and represent active proteolytic centers. We currently investigate which nuclear proteins are degraded within such proteolytic centers and the consequences for gene expression. Since xenobiotic-induced nuclear inclusions exactly mimic those observed in polyQ-expansion diseases, our research contributes to elucidate the role of protein fibrillation in neurodegeneration and neurodegenerative disease.

Nanoparticle-induced neural phenotypes in cell culture and C. elegans

Identifying nanomaterial-bio-interactions is imperative due to the broad introduction of nanoparticle applications and their distribution. We investigate widespread protein aggregation in the soil nematode C. elegans ranging from induction of amyloid in nucleoli of intestinal cells to facilitation of protein aggregation in body wall muscles and axons of neural cells. Proteomic screening identifies segregation of proteins belonging to the gene ontology group of "protein folding, proteolysis and stress response" in an SDS-resistant aggregome network. Network proteins include chaperones, heat shock proteins and subunits of the 26S proteasome which are all decisively involved in protein homeostasis. The analysis of a reporter worm for serotonergic neural cells reveals xenobiotic-induced protein aggregation in axons of HSN neurons, where presynaptic accumulation of serotonin, e.g. disturbed axonal transport reduces the capacity for neurotransmission and neural behavior. In C. elegans certain noxae promote a cascade of events including disturbance of protein homeostasis, widespread protein aggregation and inhibition of serotonergic neurotransmission which can be interrupted by anti-amyloid fibrillation compounds.

Selected Publications

01. Scharf A, Gührs KH, von Mikecz A. Anti-amyloid compounds protect from silica nanoparticle-induced neurotoxicity in the nematode C. elegans. Nanotoxicology 10: 426-435 (2016) undefinedPubMed

02. Arnhold F, Gührs KH, von Mikecz A. Amyloid domains in the cell nucleus controlled by nucleoskeletal protein lamin B1 reveal a new pathway of mercury neurotoxicity. PeerJ 3: e754 (2015) undefinedPubMed

03. von Mikecz, A. Pathology and function of nuclear amyloid: Protein homeostasis matters. Nucleus 5: 311-317 (2014) undefinedPubMed

04. Scharf A, Piechulek A, von Mikecz A. The effect of nanoparticles on the biochemical and behavioral aging phenotype of the nematode Caenorhabditis elegans. ACS Nano. 7: 10695-10703 (2013) undefinedPubMed

05. Hemmerich PH, von Mikecz AH. Defining the Subcellular Interface of Nanoparticles by Live-Cell Imaging. PLoS ONE 8: e62018 (2013) undefinedPubMed

06. Pluskota, A., Horzowski, E., Bossinger, O., and von Mikecz, A. In Caenorhabditis elegans Nanoparticle-Bio-Interactions Become Transparent: Silica-Nanoparticles Induce Reproductive Senescence. PLoS One 4: e6622 (2009) undefinedPubMed

07. von Mikecz, A. PolyQ-fibrillation in the cell nucleus: who's bad? Trends Cell Biol. 19: 685-691. (2009) undefinedPubMed

08. Chen, M., Singer, L., Scharf, A., and von Mikecz, A. Nuclear polyglutamine-containing protein aggregates as active proteolytic centers. J. Cell Biol. 180: 697-704. (2008) undefinedPubMed

09. Chen, M., and A. von Mikecz. Formation of nucleoplasmic protein aggregates impairs nuclear function in response to SiO2-nanoparticles. Exp. Cell Res. 305:51-62. (2005) undefinedPubMed

10. Rockel, T.D., Stuhlmann, D., and A. von Mikecz. Proteasomes degrade proteins in focal subdomains of the human cell nucleus. J. Cell Sci. 118: 5231-5242. (2005) undefinedPubMed

Prof. Dr.
Anna von Mikecz

Cell Biology

Prof. Dr. Anna von Mikecz

Leibniz Research Institute for Environmental Medicine
Tel.: 0211-3389-358
Fax: 0211-3190910
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