Publications by authors named "Zeynep Tansu Atasavum"

Article Synopsis
  • Neurogenesis, which helps the brain stay resilient, decreases in Alzheimer's disease (AD), leading to reactive astrocytes that hinder neurogenesis; restoring neurogenesis could potentially counteract neurodegenerative effects.
  • Researchers used a mouse model to explore the role of Nerve growth factor receptor (Ngfr) in promoting neurogenesis in astrocytes during AD, finding that Ngfr reduces a marker (Lcn2) associated with reactive astrocytes, thereby enhancing neurogenic outcomes.
  • The study indicates that by boosting Ngfr expression, it's possible to decrease amyloid plaques and improve neurogenesis, suggesting that targeting astrocytes to promote their neurogenic potential could offer new therapeutic strategies for Alzheimer's disease.
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In this chapter, we present the methodology currently used in our laboratory to generate a starPEG-MMP (starPEG)- and heparin maleimide HM06 (heparin)-based 3D cell culture system, in a hydrogel, that can be used to study human neuronal development and Alzheimer's disease (AD) pathology. A 3D cell culture system can mimic the in vivo cellular environment better than a 2D format, in which these cells exhibit neural network formation, electrophysiological activity, tissue-specific extracellular matrix (ECM) deposition, and neurotransmitter responsiveness. When treated with amyloid beta-42 (Aβ42) peptides, this system recapitulates many of the pathological effects of AD, including reduced neural stem cell proliferation, impaired neuronal network formation, dystrophic axonal ends, synaptic loss, failure to deposit ECM, elevated tau hyperphosphorylation, and formation of neurofibrillary tangles.

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L-asparaginases, which are oncolytic enzymes, have been used in clinical applications for many years. These enzymes are also important in food processing industry due to their potential in acrylamide-mitigation. In this study, the gene for l-asparaginase (GkASN) from a thermophilic bacterium, Geobacillus kaustophilus, was cloned and expressed in E.

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