<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter/><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD621</full_dataset_link><repository>bioimages</repository><figure_sub>Protocols</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>organisation</figure_sub><figure_sub>Study Protocols</figure_sub><pubmed_authors>Oliver Fackler</pubmed_authors></additional><is_claimable>false</is_claimable><name>surce data fig 3b collagen from Gallucci et </name><description>Immature Dendritic Cells (iDCs) migrate in microenvironments with distinct cell and extracellular matrix densities in vivo and contribute to HIV-1 dissemination and mounting of antiviral immune responses. Here, we find that, compared to standard 2D suspension cultures, 3D collagen as tissue-like environment alters iDC properties and their response to HIV-1 infection. iDCs adopt an elongated morphology with increased deformability in 3D collagen at unaltered activation, differentiation, cytokine secretion or responsiveness to LPS. While 3D collagen reduces HIV-1 particle uptake by iDCs, fusion efficiency is increased to elevate productive infection rates due to elevated cell surface exposure of the HIV-1 binding receptor DC-SIGN. In contrast, 3D collagen reduces HIV transfer to CD4 T-cells </description><dates><release>2023-02-08T00:00:00Z</release><modification>2023-02-08T20:28:43.196Z</modification><creation>2023-02-08T20:28:43.196Z</creation></dates><accession>S-BIAD621</accession><cross_references/></HashMap>