Összes szerző
Molnár Kinga
az alábbi absztraktok szerzői között szerepel:
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Dudás Tamás
Capillary pericytes regulate vascular tone and local blood flow in inflammation -
Aug 29 - kedd
15:00 – 15:15
Orvosi biofizika és sugárbiológia
E17
Capillary pericytes regulate vascular tone and local blood flow in inflammation
Tamás Dudás, Ádám Mészáros, Kinga Molnár, Attila Farkas, Imola Wilhelm and István Krizbai
Biological Research Centre, Szeged, Institute of Biophysics
Pericytes are the only contractile cells in cerebral capillaries. However, their role in the regulation of capillary diameter, microvascular tone and local cerebral blood flow is far from being completely understood. Furthermore, a large number of CNS disorders is accompanied by inflammatory processes. Therefore, in our present study, we investigated the role of pericytes in the maintenance of capillary tone and how inflammatory mediators could regulate pericyte contractility.
Using primary human pericytes in an in vitro collagen contraction assay, we could demonstrate that TNF-alpha, IL-6 and CCL2 induce a significant pericyte contraction. In order to prove that inflammatory mediators have similar effects in vivo, we used two photon microscopy in mice with labelled pericytes. Inflammatory mediators were administered in the vicinity of identified pericytes using microinjection techniques under continuous monitoring. TNF-alpha induced a slow but significant reduction in the capillary diameter. In addition, using line scan technology, we could show a decrease in red blood cell velocity and a reduction in the number of red blood cells passing the capillary segment in the neighbourhood of the injection. Furthermore, careful ablation of pericytes using the two-photon laser led to a late onset (after 24 hours) dilation of the capillary segment belonging to the ablated pericyte.
Our results indicate that pericytes may have an important role in the maintenance of the capillary tone, and may regulate capillary flow under inflammatory conditions.
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Péter Beatrix
Nanoparticle uptake of living cells with digested glycocalyx -
Aug 29 - kedd
15:30 – 17:00
I. Poszterszekció
P21
Nanoparticle uptake of living cells with digested glycocalyx
Beatrix Petera, Nicolett Kanyoa, Kinga Dora Kovacsa,b, Viktor Kovácsa, Inna Szekacsa, Béla Péczc, Kinga Molnárd,Hideyuki Nakanishie, Istvan Lagzi,,f,g, Robert Horvatha
a Nanobiosensorics laboratory, Institute of Technical Physics and Materials Science, Centre for Energy Research, Konkoly-Thege út 29-33, H-1121 Budapest, Hungary
b Department of Biological Physics, Eötvös University, Budapest, Hungary
c Thin Films Laboratory, Institute of Technical Physics and Materials Science, Centre for Energy Research, Konkoly-Thege út 29-33, H-1120 Budapest, Hungary
d Department of Anatomy, Cell and Developmental Biology, ELTE, Eötvös Loránd University, Pázmány Péter stny. 1/C, Budapest, H-1117, Hungary
e Department of Macromolecular Science and Engineering, Graduate School of Science and Technology, Kyoto Institute of Technology, Matsugasaki, Kyoto 606-8585, Japan
f Department of Physics, Institute of Physics, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary
g ELKH BME Condensed Matter Research Group, Műegyetem rkp. 3, Budapest H-1111, Hungary
In biomedical imaging and targeted drug delivery, functionalized nanoparticles are widely used due to their penetration into living cells. The glycocalyx is a surface sugar layer of the cells, which presumably plays an essential role in any uptake process. However, its exact function in nanoparticle uptake is still uncovered. We in situ monitored the penetration of positively charged gold nanoparticles into adhered cancer cells with or without preliminary glycocalyx digestion. During the experiments, the components of glycocalyx of HeLa cells were digested by chondroitinase ABC enzyme. The measurements were performed by applying a high-throughput label-free resonant waveguide grating biosensor. The positively charged gold nanoparticles were used with different sizes (S, M, L). Negatively charged citrate-capped tannic acid nanoparticles, and other types of glycocalyx digesting enzymes were also applied in control experiments. The biosensor data confirmed the cellular uptake of the functionalized nanoparticles with an active process, which was verified by transmission electron microscopy [1,2]. Based on the findings we conclude that the components of gylcocalyx control the uptake process in size- and charge-dependent manner, and the possible roles of various glycocalyx components were highlighted.
Acknowledgements
This work was supported by the National Research, Development, and Innovation Office (Grant Numbers: PD 131543 for B.P., ELKH topic-fund, "Élvonal" KKP_19 TKP2022-EGA-04 grants).
References
[1] B. Peter, N. Kanyo, K. D. Kovacs, V. Kovács, I. Szekacs, B. Pécz, K. Molnár, H. Nakanishi, I. Lagzi, R. Horvath. Glycocalyx components detune the cellular uptake of gold nanoparticles in a size- and charge-dependent manner. ACS Applied Bio Materials, 2023.
[2] B. Peter, I. Lagzi, S. Teraji, H. Nakanishi, L. Cervenak, D. Zámbó, A. Deák, K. Molnár, M. Truszka, I. Szekacs, R. Horvath. Interaction of positively charged gold nanoparticles with cancer cells monitored by an in situ label-free optical biosensor and transmission electron microscopy. ACS Applied Materials & Interfaces, 2018.
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Végh Attila Gergely
The force awakens: mechanical interaction of metastatic tumor cells with the neurovascular unit -
Aug 30 - szerda
14:00 – 14:18
Sejtanalitika biofizikai megközelítéssel
E32
The force awakens: mechanical interaction of metastatic tumor cells with the neurovascular unit
Attila Gergely Végh1, Katalin Csonti1,2,3, Csilla Fazakas1, Kinga Molnár1, Imola Wilhelm1,4 and István Krizbai1,4
1 Biological Research Centre, Szeged, Institute of Biophysics
2 Doctoral School of Physics, University of Szeged
3 Semilab Semiconductor Physics Laboratory Co. Ltd., Budapest
4 Institute of Life Sciences, Vasile Goldis Western University, Arad
The central nervous system has prominent defense lines, however, most of the malignancies detected within the brain parenchyma are of metastatic origin. As the brain lacks classical lymphatic circulation, the primordial way for metastasis relies on hematogenous routes. The first and probably the most crucial step for invading tumor cells relies on their interaction with the neurovascular unit. The neurovascular unit plays crucial role in the maintenance of the proper homeostasis of the central nervous system [1]. Endothelial cells and pericytes are the most exposed to mechanical stresses their mechanobiology is of primordial importance [2]. Furthermore, tumor cell derived extracellular vesicles might play key role in pre-metastatic niche formation and might be involved in metastatic organotropism [3].
Single cell-force spectroscopy was applied to investigate the adhesive properties of living breast adenocarcinoma cells to confluent layers of brain endothelial cells and pericytes. Cell type dependent adhesion characteristics were found as well as the existence of metastatic potential related nanomechanical differences between the studied tumor cells, relying partly on membrane tether dynamics. Apparent mechanical properties such as elasticity, maximal adhesion force, number, size and distance of individual rupture events have been found cell type dependent, correlating with their metastatic abilities. Additionally, tumor cell derived extracellular vesicles alter the adhesive properties of tumor cells to brain endothelial layer. Exploring the mechanobiology of constituent of the neurovascular unit could not only lead to a better understanding of their function but could also help to identify novel targets for the improvement of its barrier function.
References
[1] J. Gállego Pérez-Larraya and J. Hildebrand, “Brain metastases,” Handb. Clin. Neurol., vol. 121, pp. 1143–1157, 2014, doi: 10.1016/B978-0-7020-4088-7.00077-8.
[2] I. Wilhelm, C. Fazakas, K. Molnár, A. G. Végh, J. Haskó, and I. A. Krizbai, “Foe or friend? Janus-faces of the neurovascular unit in the formation of brain metastases,” J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab., p. 271678X17732025, Jan. 2017, doi: 10.1177/0271678X17732025.
[3] Y. Guo et al., “Effects of exosomes on pre-metastatic niche formation in tumors,” Mol. Cancer, vol. 18, no. 1, p. 39, Mar. 2019, doi: 10.1186/s12943-019-0995-1.