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Mitochondrial Physiology

Mitochondrial Physiology

Our research group focuses on the role of mitochondria in physiological and pathophysiological processes of the cell and organism. Mitochondria are the main source of cellular energy, ATP, which is essential for maintaining vital cell functions. Additionally, mitochondrial metabolism also leads to the production of oxygen radicals, reactive molecules that have a negative impact on the cell functioning, i.e. irreversible damage of cellular proteins, lipids and DNA (both mitochondrial and nuclear). Such prolonged oxidative stress in extreme cases leads to cell death. Chronic, albeit relatively moderate oxidative stress accompanies number of pathophysiological disorders including neurodegenerative diseases (such as Parkinson's and Alzheimer's disease), but for example also type 2 diabetes and pulmonary hypertension, the etiology of which we study in our laboratory. In case of irreversible damage mitochondria must be removed by specific pathway of autophagy, called mitophagy. This process is crucial for mitochondrial quality control process, disruption of which is accompanied by a number of diseases such as type 2 diabetes, which is where we study the mitophagy. Moreover, mitochondria are semiautonomous organelles for they have mitochondrial DNA (mtDNA). Genetic manipulation of the mtDNA is rather complicated and yet there has not been found satisfactory method which would allow us for e.g. gene silencing or in-situ quantification of genetic mutations in mtDNA. The development of such techniques is one of out goals. Since mitochondria are rather small organelles and resolution of commonly available light and fluorescence microscopy is not sufficient to study certain aspects of their morphology, we employ special super-resolution fluorescence microscopy. The prototype of such microscope we have recently purchased for our department. We develop further methodologies of “nanoscopy” to study mitochondrial morphology and function. Finally, we study the role of mitochondrial signaling in cancer cells and cancer-specific enzymatic pathways, study of which could be essential for the development of future anticancer drugs.

Concerning applied research, we also develop novel drug carriers to transport specific anticancer drugs called photosensitizers into cancer tissues. Our findings have been patented in Industrial Property Office of the Czech Republic.

 

 

Projects

Publications

Jabůrek, Martin - Ježek, Jan - Ježek, Petr . Cytoprotective activity of mitochondrial uncoupling protein‐2 in lung and spleen . FEBS Open Bio 2018, roč. 8, 4, p. 692-701 . IF = 1.782 [ASEP] [ doi ]
Kahancová, Anežka - Sklenář, Filip - Ježek, Petr - Dlasková, Andrea . Regulation of glucose-stimulated insulin secretion by ATPase Inhibitory Factor 1 (IF1) . FEBS Letters 2018, roč. 592, 6, p. 999-1009 . IF = 2.999 [ASEP] [ doi ]
D'Alessandro, A. - El Kasmi, K. C. - Plecitá-Hlavatá, Lydie - Ježek, Petr - Li, M. - Zhang, H. - Gupte, S. A. - Stenmark, K. R. Hallmarks of Pulmonary Hypertension: Mesenchymal and Inflammatory Cell Metabolic Reprogramming . Antioxidants & Redox Signaling 2018, roč. 28, 3, p. 230-250 . IF = 6.530 [ASEP] [ doi ]
Zhang, H. - Wang, D. - Li, M. - Plecitá-Hlavatá, Lydie - D'Alessandro, A. - Tauber, Jan - Riddle, S. - Kumar, S. - Flockton, A. - McKeon, B. A. - Frid, M. G. - Reisz, J. A. - Caruso, P. - El Kasmi, K. C. - Ježek, Petr - Morrell, N. W. - Hu, Ch.-J. - Stenmark, K. R. Metabolic and Proliferative State of Vascular Adventitial Fibroblasts in Pulmonary Hypertension Is Regulated Through a MicroRNA-124/PTBP1 (Polypyrimidine Tract Binding Protein 1)/Pyruvate Kinase Muscle Axis . Circulation.. 2017, roč. 136, 25, p. 2468-2485 . IF = 18.88 [ASEP] [ doi ]
Špaček, Tomáš - Pavluch, Vojtěch - Alán, Lukáš - Capková, Nikola - Engstová, Hana - Dlasková, Andrea - Berková, Z. - Saudek, F. - Ježek, Petr . Nkx6.1 decline accompanies mitochondrial DNA reduction but subtle nucleoid size decrease in pancreatic islet beta-cells of diabetic Goto Kakizaki rats . Scientific Reports.. 2017, roč. 7, Nov 15, článku 15674 . IF = 4.122 [ASEP] [ doi ]

Contacts

Institute of Physiology AS CR, v.v.l.
Depertment of Mitochondrial Physiology
Vídeňská 1083
14220 Prague 4
Czech Republic
tel. +420 241 062 760
  +420 241 065 585
fax. +420 241 062 488
 

petr.jezek@fgu.cas.cz

andrea.dlaskova@fgu.cas.cz

People

  RNDr. Petr Ježek, DrSc.
head of the department
  Ing. Andrea Dlasková, Ph.D.
deputy head of the department
  Mgr. Hana Engstová, Ph.D.
senior researcher
 

Mgr. Blanka Holendová, Ph.D.

senior researcher

  Mgr. Martin Jabůrek, Ph.D.
senior researcher
  RNDr. Jan Ježek, Ph.D.
senior researcher
  RNDr. Lýdie Plecitá, Ph.D.
senior researcher
  RNDr. Katarína Smolková, Ph.D.
senior researcher
  Ing. Tomáš Špaček, Ph.D.
senior researcher
  Mgr. Jitka Špačková (Šantorová), Ph.D.
senior researcher
  Ing. Jan Tauber, Ph.D.
senior researcher
 

Alberto Leguina Ruzzi, Ph.D.

senior researcher

  Ing. Anežka Kahancová
PhD student
 

Mgr. Vojtěch Pavluch

PhD student

 

Ing. Pavla Průchová

PhD student

 

Bc. Filip Sklenář

pregraduate student

 

Štěpánka Tučková

pregraduate student

 

Alexandra Urbančoková

pregraduate student

  Jitka Smiková
lab technician
  Ludmila Šimečková
lab technician
  Jana Vaicová
lab technician

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