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Ravni izražanja in aktivnosti katepsina X in izooblik enolaze v fenotipsko različnih populacijah celic SH-SY5Y
ID Horvat, Anja (Avtor), ID Pišlar, Anja (Mentor) Več o mentorju... Povezava se odpre v novem oknu, ID Horvat, Selena (Komentor)

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Izvleček
Osnovna gradbena enota centralnega živčnega sistema je nevron. Za preučevanje procesov v nevronih se uporabljajo številni in vitro celični modeli in med njimi tudi diferencirane celice SH-SY5Y. Pomembno vlogo pri diferenciaciji nevronov imajo nevrotrofični dejavniki, katerim podobno delovanje izkazuje tudi glikolitični encim γ-enolaza. Nevrotrofično aktivnost γ-enolaze uravnava cisteinska peptidaza katepsin X s proteolitično cepitvijo zadnjih dveh aminokislin na C-koncu γ-enolaze. V sklopu magistrske naloge smo določili ravni izražanja in aktivnosti katepsina X ter izooblik enolaze v fenotipsko različnih populacijah celic SH-SY5Y, katere sestavljajo trije različni fenotipi, in sicer epiteljiski S-tip, nevronski N-tip in vmesni I-tip celic SH-SY5Y. Najprej smo vzpostavili protokol za diferenciacijo in uspešno obogatitev posameznih populacij celic SH-SY5Y, pri čemer smo spreminjali podlago, sestavo gojišča in čas gojenja celic, kar smo spremljali s pomočjo svetlobnega invertnega mikroskopa. 10-dnevno gojenje celic v gojišču z zmanjšano vsebnostjo seruma ob dodani 5 µM retinojski kislini se je izkazalo za uspešno za pridobitev obogatenih populacij celic tipa S in N. Z vrednotenjema izražanja označevalcev s pomočjo prenosa western in konfokalne mikroskopije smo opazili, da je izražanje označevalca epitelijskih celic vimentina povišano v populaciji celic tipa S ter izražanje označevalcev nevronov, in sicer tirozin hidroksilaze in z rastjo povezan protein 43, povišano v populaciji celic tipa N. Na obogatenih populacijah S- in N-tipa smo preučili raven izražanja katepsina X in njegovo aktivnost kot tudi raven izražanje tarče katepsina X v nevronskih celicah, enolaze. Pokazali smo, da je največje izražanje proteina katepsina X v celicah tipa N, medtem ko je bila največja aktivnost katepsina X v celicah tipa S. Izražanje izooblike α-enolaze je neodvisno od posamezne populacije celic SH-SY5Y, medtem ko je višja raven izooblike γ-enolaze značilna za N-tip celic SH-SY5Y, kar smo vrednotili s prenosom western in encimsko-imunskim testom. Izražanje aktivne oblike γ-enolaze je bilo povišano v obeh populacijah celic SH-SY5Y napram kontrolnim celicam, vendar je bilo povišanje izrazitejše v N-tipu celic SH-SY5Y. S pomočjo konfokalne mikroskopije smo pokazali močnejšo ko-lokalizacijo γ-enolaze in katepsina X v celicah N-tipa, predvsem v izrastkih celic, t.i. nevritih, kar nakazuje na vlogo, ki jo ima γ-enolaza v procesu rasti in diferenciacije nevronov ter njeno uravnavanje s katepsinom X.

Jezik:Slovenski jezik
Ključne besede:celice SH-SY5Y, diferenciacija, enolaza, nevrotrofična aktivnost, katepsin X
Vrsta gradiva:Magistrsko delo/naloga
Organizacija:FFA - Fakulteta za farmacijo
Leto izida:2024
PID:20.500.12556/RUL-161711 Povezava se odpre v novem oknu
Datum objave v RUL:13.09.2024
Število ogledov:169
Število prenosov:107
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Sekundarni jezik

Jezik:Angleški jezik
Naslov:Expression and activity levels of cathepsin X and enolase isoforms in phenotypically distinct populations of SH-SY5Y cells
Izvleček:
The basic structure of the central nervous system is the neuron. Numerous in vitro cellular models are used to study processes in neurons, including differentiated SH-SY5Y cells. Neurotrophic factors play an important role in the differentiation of neurons, and the glycolytic enzyme γ-enolase also shows similar activity. The neurotrophic activity of γ-enolase is regulated by the cysteine peptidase cathepsin X, which proteolytically cleaves the last two amino acids from the C-terminal domain of γ-enolase. In this master's thesis, we determined the levels of protein expression and activity of cathepsin X and protein expression of enolase isoforms in phenotypically different populations of SH-SY5Y cells, which consist of three distinct phenotypes: epithelial S-type, neuronal N-type, and intermediate I-type SH-SY5Y cells. We first established a protocol for the differentiation and successful enrichment of individual populations of SH-SY5Y cells by modifying the cell culture plate coating, culture medium composition and cell growth time, which we monitored using a light inverted microscope. A 10-day cell culture growing in reduced serum medium content and the addition of 5 µM retinoic acid was found to be successful in obtaining enriched populations of S- and N-type cells. Through the assessment of marker expression using Western blotting and confocal microscopy, we observed that the expression of the epithelial cell marker vimentin was elevated in the S-type cell population, while the expression of neuronal markers, specifically tyrosine hydroxylase and growth-associated protein 43, was elevated in the N-type cell population. In the enriched populations of S- and N-type cells, we examined the expression levels of cathepsin X and its activity, as well as the expression levels of the target of cathepsin X in neuronal cells, enolase. We demonstrated that the highest expression of the cathepsin X protein was found in N-type cells, while the highest activity of cathepsin X was observed in S-type cells. The expression of the α-enolase isoform was independent of the individual SH-SY5Y cell populations, while a higher level of the γ-enolase isoform was characteristic of N-type SH-SY5Y cells, as evaluated by Western blotting and enzyme-linked immunosorbent assay. The expression of the active form of γ-enolase was elevated in both populations of SH-SY5Y cells compared to the control cells, nevertheless the increase was more noticeable in N-type SH-SY5Y cells. Using confocal microscopy, we demonstrated stronger co-localization of γ-enolase and cathepsin X in N-type cells, particularly in the cell extensions, so-called neurites, which suggests a role for γ-enolase in the process of neuronal growth and differentiation, and its regulation by cathepsin X.

Ključne besede:SH-SY5Y cells, differentiation, enolase, neurotrophic activity, cathepsin X

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