The Effect of Extracellular Matrix on the Differentiation of Mouse Embryonic Stem Cells

dc.contributor.author Ozdil, Berrin
dc.contributor.author Guler, Gunnur
dc.contributor.author Acikgoz, Eda
dc.contributor.author Kocaturk, Duygu Calik
dc.contributor.author Aktug, Huseyin
dc.date.accessioned 2025-05-10T17:34:56Z
dc.date.available 2025-05-10T17:34:56Z
dc.date.issued 2020
dc.description Calik Kocaturk, Duygu/0000-0001-5995-8967; Guler, Gunnur/0000-0002-8485-7372; Ozdil, Berrin/0000-0001-6081-2308; Acikgoz, Eda/0000-0002-6772-3081; Aktug, Huseyin/0000-0003-4150-8495 en_US
dc.description.abstract Embryonic stem cells (ESCs) are promising research materials to investigate cell fate determination since they have the capability to differentiate. Stem cell differentiation has been extensively studied with various microenvironment mimicking structures to modify cellular dynamics associated with the cell-extracellular matrix (ECM) interactions and cell-cell communications. In the current study, our aim was to determine the effect of microenvironmental proteins with different concentrations on the capacity and differentiation capability of mouse ESCs (mESCs), combining the biochemical assays, imaging techniques, Fourier transform infrared (FTIR) spectroscopy, and unsupervised multivariate analysis. Based on our data, coating the surface of mESCs with Matrigel, used as an acellular matrix substrate, resulted in morphological and biochemical changes. mESCs exhibited alterations in their phenotype after growing on the Matrigel-coated surfaces, including their differentiation capacity, cell cycle phase pattern, membrane fluidity, and metabolic activities. In conclusion, mESCs can be stimulated physiologically, chemically, or mechanically to convert them a new phenotype. Thus, identification of ESCs' behavior in the acellular microenvironment could be vital to elucidate the mechanism of diseases. It might also be promising to control the cell fate in the field of tissue engineering. en_US
dc.identifier.doi 10.1002/jcb.29159
dc.identifier.issn 0730-2312
dc.identifier.issn 1097-4644
dc.identifier.scopus 2-s2.0-85067362123
dc.identifier.uri https://doi.org/10.1002/jcb.29159
dc.identifier.uri https://hdl.handle.net/20.500.14720/13972
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cell Fate en_US
dc.subject Differentiation en_US
dc.subject Ftir Spectroscopy en_US
dc.subject Matrigel en_US
dc.subject Mouse Embryonic Stem Cell en_US
dc.title The Effect of Extracellular Matrix on the Differentiation of Mouse Embryonic Stem Cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Calik Kocaturk, Duygu/0000-0001-5995-8967
gdc.author.id Guler, Gunnur/0000-0002-8485-7372
gdc.author.id Ozdil, Berrin/0000-0001-6081-2308
gdc.author.id Acikgoz, Eda/0000-0002-6772-3081
gdc.author.id Aktug, Huseyin/0000-0003-4150-8495
gdc.author.scopusid 56301503200
gdc.author.scopusid 37010966300
gdc.author.scopusid 56364984200
gdc.author.scopusid 57208204702
gdc.author.scopusid 8633854300
gdc.author.wosid Acikgoz, Eda/W-2171-2017
gdc.author.wosid Güler, Günnur/Aah-6852-2021
gdc.author.wosid Özdil, Berrin/Gqb-2824-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Ozdil, Berrin; Acikgoz, Eda; Kocaturk, Duygu Calik; Aktug, Huseyin] Ege Univ, Fac Med, Dept Histol & Embryol, TR-35100 Izmir, Turkey; [Ozdil, Berrin] Suleyman Demirel Univ, Fac Med, Dept Histol & Embryol, Isparta, Turkey; [Guler, Gunnur] Izmir Univ Econ, Dept Biomed Engn, TR-35330 Izmir, Turkey; [Guler, Gunnur] Ege Univ, Ctr Drug Res & Dev & Pharmacokinet Applicat, Izmir, Turkey; [Acikgoz, Eda] Yuzuncu Yil Univ, Fac Med, Dept Histol & Embryol, Van, Turkey en_US
gdc.description.endpage 283 en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 269 en_US
gdc.description.volume 121 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 31168838
gdc.identifier.wos WOS:000498739700025
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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