<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(1)</volume><submitter>Xue W</submitter><pubmed_abstract>The spinal cord possesses highly complex, finely organized cytoarchitecture guided by two dorsoventral morphogenic organizing centers. Thus, generation of human spinal cord tissue &lt;i>in vitro&lt;/i> is challenging. Here, we demonstrated a novel method for generation of human dorsoventral spinal cord organoids using composite scaffolds. Specifically, the spinal cord ventralizing signaling Shh agonist (SAG) was loaded into a porous chitosan microsphere (PCSM), then thermosensitive Matrigel was coated on the surface to form composite microspheres with functional sustained-release SAG, termed as PCSM-Matrigel@SAG. Using PCSM-Matrigel@SAG as the core to induce 3D engineering of human spinal cord organoids from human pluripotent stem cells (ehSC-organoids), we found ehSC-organoids could form dorsov</pubmed_abstract><journal>iScience</journal><pagination>105898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9840144</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Generation of dorsoventral human spinal cord organoids via functionalizing composite scaffold for drug testing.</pubmed_title><pmcid>PMC9840144</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Xue W</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Ren L</pubmed_authors><pubmed_authors>Shao Z</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Li B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Generation of dorsoventral human spinal cord organoids via functionalizing composite scaffold for drug testing.</name><description>The spinal cord possesses highly complex, finely organized cytoarchitecture guided by two dorsoventral morphogenic organizing centers. Thus, generation of human spinal cord tissue &lt;i>in vitro&lt;/i> is challenging. Here, we demonstrated a novel method for generation of human dorsoventral spinal cord organoids using composite scaffolds. Specifically, the spinal cord ventralizing signaling Shh agonist (SAG) was loaded into a porous chitosan microsphere (PCSM), then thermosensitive Matrigel was coated on the surface to form composite microspheres with functional sustained-release SAG, termed as PCSM-Matrigel@SAG. Using PCSM-Matrigel@SAG as the core to induce 3D engineering of human spinal cord organoids from human pluripotent stem cells (ehSC-organoids), we found ehSC-organoids could form dorsov</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-05-27T23:23:19.712Z</modification><creation>2024-12-03T22:58:59.662Z</creation></dates><accession>S-EPMC9840144</accession><cross_references><pubmed>36647382</pubmed><doi>10.1016/j.isci.2022.105898</doi></cross_references></HashMap>