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The role of the Wnt signaling pathway in the regeneration following ischemic brain injury
Kriška, Ján ; Anděrová, Miroslava (advisor) ; Stuchlík, Aleš (referee) ; Zíková, Martina (referee)
The role of the Wnt signaling pathway in the regeneration following ischemic brain injury Focal cerebral ischemia results in the loss of neural cells, which may cause permanent disability. At the same time, there are precursor cells (neural stem/progenitor cells and NG2 glia) that naturally reside in the postnatal brain and may proliferate and give rise to other cell types. Their fate is to a large extent influenced by morphogens of the Wnt and Shh family. However, the role of these cellular pathways in differentiation of precursor cells is still enigmatic. For this reason, we employed transgenic mice that enabled us to inhibit or hyper-activate the canonical Wnt signaling pathway, or to map the fate of NG2 cells. The induction of ischemia was achieved by the occlusion of the middle cerebral artery. The changes in the differentiation potential were characterized at the mRNA, protein, and functional levels. First, we evaluated neural stem/progenitor cells isolated from neonatal mice under physiological conditions and found out that Wnt signaling promotes neurogenesis and suppresses gliogenesis. Next, we focused on adult mice and detected a smaller impact of Wnt signaling on their differentiation potential. Nonetheless, its effect was more profound after the induction of ischemia, as we identified...
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Cellular and molecular mechanisms of activation of thermally sensitive TRP ion channels
Máčiková, Lucie ; Vlachová, Viktorie (advisor) ; Anděrová, Miroslava (referee) ; Jakubík, Jan (referee)
The transient receptor potential (TRP) are cation channels mostly permeable to both monovalent and divalent cations. ThermoTRP is a specific group of directly thermally activated TRP channels. The vanilloid transient receptor potential 3 (TRPV3) is an ion channel widely expressed in keratinocytes, that is implicated in the regulation of skin homeostasis, thermo- sensing, nociception and development of itch sensation. Our results show the importance of the cytoplasmic inter-subunit interface in the heat sensitivity of TRPV3. As there is a structural analogy within the vanilloid receptors, our hypothesis of the identified important region is supposed to be valid also for other thermally activated TRPV receptors (TRPV1, TRPV2 and TRPV4). We have proved that TRPV3 is a substrate for ERK1/2 protein kinase (kinase regulated by extracellular signal 1 and 2) and we have identified TRPV3 phosphorylation sites that may be direct targets for ERK1/2. Of these residues, threonine 264 has been shown to be the main phosphorylation site responsible for TRPV3 sensitization mediated by ERK kinase. In human keratinocytes, the phosphorylation might be physiologically and pathophysiologically important in processes of TRPV3 sensitization mediated by MAPK signaling pathway. The transient receptor potential ankyrin 1...
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The role of AQP4 and TRPV4 channels in the ischemic brain edema: focusing on glial cells
Kročianová, Daniela ; Anděrová, Miroslava (advisor) ; Máčiková, Lucie (referee)
Cerebral ischemia, also known as stroke, is one of the most common causes of death. It is accompanied by the formation of edema, which can be characterized as an influx of water and osmolytes into the brain, causing volume alterations. We recognize two types of cerebral edema - vasogenic, characterized by the disruption of the blood-brain barrier (BBB) and increase of the extracellular volume, and cytotoxic, caused by the increase of the volume of cells, mainly glia. The major contributors to the formation of cytotoxic edema are the astrocytes, which, in physiological conditions, are responsible for the maintenance of the BBB and keeping the homeostasis of the brain and spinal cord or central nervous system. The mechanism responsible for the process of volume and osmotic changes are the transmembrane channels, mainly aquaporin 4 (AQP4) and transient receptor potential vanilloid 4 (TRPV4). AQP4 is the main pathway for water influx as well as efflux when the edema subsides. TRPV4 is likely responsible for the maintenance of the osmotic balance of the organism, although its precise role in the formation of the edema has not yet been fully elucidated. The main aim of this thesis was to categorize the types of cerebral ischemia and edema, and to describe the process of cerebral edema formation and the...
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The role of AQP4 and TRVP4 channels in the ischemic brain edema: focusing on glial cells.
Kročianová, Daniela ; Anděrová, Miroslava (advisor) ; Máčiková, Lucie (referee)
Cerebral ischemia, also known as stroke, is one of the most common causes of death. It is accompanied by the formation of edema, which can be characterized as an influx of water and osmolytes into the brain, causing volume alterations. We recognize two types of cerebral edema - vasogenic, characterized by the disruption of the blood-brain barrier (BBB) and increase of the extracellular volume, and cytotoxic, caused by the increase of the volume of cells, mainly glia. The major contributors to the formation of cytotoxic edema are the astrocytes, which, in physiological conditions, are responsible for the maintenance of the BBB and keeping the homeostasis of the brain and spinal cord or central nervous system. The mechanism responsible for the process of volume and osmotic changes are the transmembrane channels, mainly aquaporin 4 (AQP4) and transient receptor potential vanilloid 4 (TRPV4). AQP4 is the main pathway for water influx as well as efflux when the edema subsides. TRPV4 is likely responsible for the maintenance of the osmotic balance of the organism, although its precise role in the formation of the edema has not yet been fully elucidated. The main aim of this thesis was to categorize the types of cerebral ischemia and edema, and to describe the process of cerebral edema formation and the...
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The Role of Aquaporin 4 channels and Transient Receptor Potential Vanilloid 4 channels in astrocytic swelling
Heřmanová, Zuzana ; Anděrová, Miroslava (advisor) ; Machová Urdzíková, Lucia (referee)
Astrocytes posses a wide range of functions within the brain. In response to ischemic conditions they swell due to increased uptake of osmolytes and they are mainly responsible for cytotoxic edema formation. However, they are also able to regulate their volume by releasing osmolytes together with water via the process of regulatory volume decrease (RVD). The Aquaporin 4 (AQP4) channel and Transient receptor potential vanilloid 4 (TRPV4) channel are suspected to be strongly involved in these processes of astrocytic volume regulation. The goal of the present diploma thesis was to clarify the role of both channels in astrocytic swelling in situ. For our experiments we used a subpopulation of green fluorescent protein-labelled astrocytes from AQP4-deficient (AQP4-/- ), TRPV4-deficient (TRPV4-/- ) and control (Ctrl) mice. Cell volume alterations were induced in acute brain slices by hypoosmotic stress or by oxygen-glucose deprivation (OGD). Data were quantified using fluorescence intensity-based approach in the whole cells and in astrocytic endfeet. Our results indicate, that there is no difference in astrocytic swelling or cell volume recovery between astrocytes from AQP4-/- , TRPV4-/- and control mice when exposed to hypoosmotic stress. On the contrary, volume changes induced by OGD varied...
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Steroid - NMDA receptor interaction: Structure-activity study and effect on mutant forms of human NMDA receptors
Krausová, Barbora ; Vyklický, Ladislav (advisor) ; Anděrová, Miroslava (referee) ; Tureček, Rostislav (referee)
N-methyl-D-aspartate (NMDA) receptors are glutamate-gated calcium permeable ion channels that play a key role in excitatory synaptic transmission and plasticity, and their dysfunction underlies several neuropsychiatric disorders. The overactivation of NMDA receptors by tonically increased ambient glutamate can lead to excitotoxicity, associated with various acute and chronic neurological disorders, such as ischemia, Alzheimer and Parkinson's disease, epilepsy or depression. On the opposite, NMDA receptor hypofunction is thought to be implicated in autism, schizophrenia, or intellectual disability. Recent DNA screening for neurological and psychiatric patients revealed numerous mutations in genes encoding for NMDA receptor subunits. The activity of NMDA receptors is influenced by a wide variety of allosteric modulators, including neurosteroids that could both inhibit and potentiate the activity of NMDA receptors, which makes them promising therapeutic targets. In this thesis, we describe new classes of neurosteroid analogues which possess structural modifications at carbons C3 and C17 of the steroidal core, and analogues without D-ring region (perhydrophenanthrenes). We evaluated the structure-activity relationship (SAR) for their modulatory effect on recombinant GluN1/GluN2B receptors. Our results...
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DISP3/PTCHD2 function in neural cells
Konířová, Jana ; Bartůněk, Petr (advisor) ; Anděrová, Miroslava (referee) ; Pacherník, Jiří (referee)
DISP3 protein, also known as PTCHD2, belongs to the PTCHD family of proteins, which contain a sterol-sensing domain in their structure. The expression of the Disp3 gene is high in neural tissues and is regulated by thyroid hormone. The DISP3 gene is associated with development and progression of certain types of tumors, as well as with development of some neural pathologies. Neural stem cells also display high expression of the Disp3 gene. Neural stem cells are defined by their capability to self-renewal and capacity to differentiate into the basic types of neural cells - neurons, astrocytes, and oligodendrocytes. Precise regulation of the balance between proliferation and differentiation of neural stem cells is crucial for development of the central nervous system and its subsequent proper functioning, and disruption of this balance may lead to development of various pathologies. In this work we mainly focused on describing the function of the DISP3 protein in neural cells and tissues. We have shown that during differentiation of neural stem cells, the expression of the Disp3 gene is significant decreased. Furthermore, we have found that in neural stem and progenitor cells, the increased expression of the Disp3 gene promotes their proliferation. Moreover, when Disp3 expression was disrupted, the...
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Glial cells and their role in amyotrophic lateral sclerosis
Vaňátko, Ondřej ; Anděrová, Miroslava (advisor) ; Černý, Jan (referee)
Amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease) is a progressive neurodegenerative disorder. It affects upper and lower motor neurons in the brain motor cortex, the brain stem and the spinal cord, causing their death, which results in denervation of voluntary muscles. Progressive muscle weakness and atrophy throughout the entire body gradually leads to worsening of the ability to move, speak, chew, swallow and eventually breath. Ultimately it results in affected individual's death due to respiratory muscle failure. Although first identified in 1869, no cure for ALS has been yet found. While early studies focused mainly on the research of motor neurons themselves, the attention has shifted towards glial cells in the past two decades. Glial cells are essential for proper neuron functioning and survival and it appears that they play a major role in ALS progression. The goal of this thesis is to review and summarize findings on the role of glial cells in ALS over the last years, focusing on four specific types of glial cells, namely astrocytes, microglia, oligodendrocytes and NG2-glia. Key words: amyotrophic lateral sclerosis, ALS, motor neuron, glia, astrocyte, microglia, oligodendrocyte, NG2-glia
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