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<title>Acta Universitatis Lodziensis. Folia Biologica et Oecologica 12/2016</title>
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<dc:date>2026-04-04T05:07:43Z</dc:date>
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<title>The role of the Amyloid Precursor Protein mutations and PERK-dependent signaling pathways in the pathogenesis of Alzheimer’s disease</title>
<link>http://hdl.handle.net/11089/20775</link>
<description>The role of the Amyloid Precursor Protein mutations and PERK-dependent signaling pathways in the pathogenesis of Alzheimer’s disease
Rozpędek, Wioletta; Nowak, Alicja; Pytel, Dariusz; Lewko, Dawid; Diehl, J. Alan; Majsterek, Ireneusz
Alzheimer’s disease (AD) is a highly complex, progressive, age-related neurodegenerative human disease entity. The genetic basis of AD is strictly connected with occurrence of mutations in Amyloid Precursor (APP) gene on chromosome 21. Molecular mechanism that leads to AD development still remains unclear. Recent data reported that it is closely correlated with Endoplasmic Reticulum (ER) stress conditions, which subsequently activate Unfolded Protein Response (UPR) signaling pathways, via the induction of protein kinase RNA-like endoplasmic reticulum kinase (PERK), as a self-protective, adaptive response to adverse stress conditions. That results in the attenuation of global protein synthesis and, on the contrary, selective translation of Activating Transcriptor Factor 4 (ATF4) and secretase β. Interestingly, under prolonged, severe ER stress UPR may switch its signal into apoptotic cell death. That ensues by ATF4-CHOP-mediated activation of a range of pro-apoptotic genes and, on the other hand, downregulation of the expression of the anti-apoptotic protein B-cell lymphoma 2 (Bcl-2) genes. Current investigations suggest that inhibitions of PERK activity may contribute to the attenuation of the deposition of toxic senile plaques in the brain tissue and, as a result, prevent degeneration of neurons and decline in cognitive abilities.
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<dc:date>2017-02-07T00:00:00Z</dc:date>
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<title>Adipose-derived stem cells: a review of osteogenesis differentiation</title>
<link>http://hdl.handle.net/11089/20774</link>
<description>Adipose-derived stem cells: a review of osteogenesis differentiation
Skubis, Aleksandra; Sikora, Bartosz; Zmarzły, Nikola; Wojdas, Emilia; Mazurek, Urszula
Second part of manuscript based on osteogenesis differentiation of stem cells. Bones are highly regenerative organs but there are still many problems with therapy of large bone defects. Sometimes there is necessary to make a replacement or expansion new bone tissue. Stem cells might be a good solution for this especially ADSCs which manage differentiate into osteoblast in in vitro and in vivo conditions.
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<dc:date>2017-02-07T00:00:00Z</dc:date>
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<title>Methods for eradication of the biofilms formed by opportunistic pathogens using novel techniques – A review</title>
<link>http://hdl.handle.net/11089/20773</link>
<description>Methods for eradication of the biofilms formed by opportunistic pathogens using novel techniques – A review
Zabielska, Julia; Tyfa, Agnieszka; Kunicka-Styczyńska, Alina
The inconvenient environmental conditions force microorganisms to colonize either abiotic surfaces or animal and plant tissues and, therefore, form more resistant structures – biofilms. The phenomenon of microbial adherence, opportunistic pathogens in particular, is of a great concern. Colonization of medical devices and biofilm formation on their surface, may lead to severe infections mainly in humans with impaired immune system. Although, current research consider various methods for prevention of microbial biofilms formation, still, once a biofilm is formed, its elimination is almost impossible. This study focuses on the overview of novel methods applied for eradication of mature opportunistic pathogens' biofilms. Among various techniques the following: cold plasma, electric field, ultrasounds, ozonated water treatment, phagotherapy, matrix targeting enzymes, bacteriocins, synthetic chemicals and natural origin compounds used for biofilm matrix disruption were briefly described.
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<dc:date>2017-02-07T00:00:00Z</dc:date>
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<item rdf:about="http://hdl.handle.net/11089/20772">
<title>Endocannabinoid system and anticancer properties of cannabinoids</title>
<link>http://hdl.handle.net/11089/20772</link>
<description>Endocannabinoid system and anticancer properties of cannabinoids
Śledziński, Paweł; Nowak, Agnieszka; Zeyland, Joanna; Słomski, Ryszard
Cannabinoids impact human body by binding to cannabinoids receptors (CB1 and CB2). The two main phytocannabinoids are Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD). THC interacts with CB1 receptors occurring in central nervous system and is responsible for psychoactive properties of marijuana. CBD has low affinity to CB1 receptor, has no psychoactive characteristics and its medical applications can be wider. CB receptors are part of a complex machinery involved in regulation of many physiological processes – endocannabinoid system. Cannabinoids have found some applications in palliative medicine, but there are many reports concerning their anticancer affects. Agonists of CB1 receptors stimulate accumulation of ceramides in cancer cells, stress of endoplasmic reticulum (ER stress) and, in turn, apoptosis. Effects of cannabinoids showing low affinity to CB receptors is mediated probably by induction of reactive oxygen species production. Knowledge of antitumor activity of cannabinoids is still based only on preclinical studies and there is a necessity to conduct more experiments to assess the real potential of these compounds.
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<dc:date>2017-02-07T00:00:00Z</dc:date>
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