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Bioactive and chemically defined hydrogels with tunable stiffness guide cerebral organoid formation and modulate multi-omics plasticity in cerebral organoids

Isik, Melis; Okesola, Babatunde O.; Eylem, Cemil Can; Kocak, Engin; Nemutlu, Emirhan; D'Este, Matteo; Mata, Alvaro; Derkus, Burak


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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Isik, Melis</dc:creator>
  <dc:creator>Okesola, Babatunde O.</dc:creator>
  <dc:creator>Eylem, Cemil Can</dc:creator>
  <dc:creator>Kocak, Engin</dc:creator>
  <dc:creator>Nemutlu, Emirhan</dc:creator>
  <dc:creator>D'Este, Matteo</dc:creator>
  <dc:creator>Mata, Alvaro</dc:creator>
  <dc:creator>Derkus, Burak</dc:creator>
  <dc:date>2023-01-01</dc:date>
  <dc:description>Organoids are an emerging technology with great potential in human disease modelling, drug devel-opment, diagnosis, tissue engineering, and regenerative medicine. Organoids as 3D-tissue culture sys-tems have gained special attention in the past decades due to their ability to faithfully recapitulate the complexity of organ-specific tissues. Despite considerable successes in culturing physiologically relevant organoids, their real-life applications are currently limited by challenges such as scarcity of an appropri-ate biomimetic matrix. Peptide amphiphiles (PAs) due to their well-defined chemistry, tunable bioactiv-ity, and extracellular matrix (ECM)-like nanofibrous architecture represent an attractive material scaffold for organoids development. Using cerebral organoids (COs) as exemplar, we demonstrate the possibility to create bio-instructive hydrogels with tunable stiffness ranging from 0.69 kPa to 2.24 kPa to culture and induce COs growth. We used orthogonal chemistry involving oxidative coupling and supramolec-ular interactions to create two-component hydrogels integrating the bio-instructive activity and ECM -like nanofibrous architecture of a laminin-mimetic PAs (IKVAV-PA) and tunable crosslinking density of hyaluronic acid functionalized with tyramine (HA-Try). Multi-omics technology including transcriptomics, proteomics, and metabolomics reveals the induction and growth of COs in soft HA-Tyr hydrogels contain-ing PA-IKVAV such that the COs display morphology and biomolecular signatures similar to those grown in Matrigel scaffolds. Our materials hold great promise as a safe synthetic ECM for COs induction and growth. Our approach represents a well-defined alternative to animal-derived matrices for the culture of COs and might expand the applicability of organoids in basic and clinical research. Statement of significance Synthetic bio-instructive materials which display tissue-specific functionality and nanoscale architecture of the native extracellular matrix are attractive matrices for organoids development. These synthetic ma-trices are chemically defined and animal-free compared to current gold standard matrices such as Ma-trigel. Here, we developed hydrogel matrices with tunable stiffness, which incorporate laminin-mimetic peptide amphiphiles to grow and expand cerebral organoids. Using multi-omics tools, the present study provides exciting data on the effects of neuro-inductive cues on the biomolecular profiles of brain organoids. (c) 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/271188</dc:identifier>
  <dc:identifier>oai:aperta.ulakbim.gov.tr:271188</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>ACTA BIOMATERIALIA 171 16</dc:source>
  <dc:title>Bioactive and chemically defined hydrogels with tunable stiffness guide cerebral organoid formation and modulate multi-omics plasticity in cerebral organoids</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
</oai_dc:dc>
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