{"id":31516,"date":"2025-09-12T09:05:00","date_gmt":"2025-09-12T09:05:00","guid":{"rendered":"https:\/\/amelie-project.eu\/?post_type=publication&#038;p=31516"},"modified":"2025-12-17T16:47:20","modified_gmt":"2025-12-17T16:47:20","slug":"kryopraeservering-af-implanterbare-humane-skeletmuskelafledte-celle-mikrobaererkombinationer-til-brug-i-klinisk-regenerativ-medicin","status":"publish","type":"publication","link":"https:\/\/amelie-project.eu\/da\/udgivelse\/kryopraeservering-af-implanterbare-humane-skeletmuskelafledte-celle-mikrobaererkombinationer-til-brug-i-klinisk-regenerativ-medicin\/","title":{"rendered":"Kryopr\u00e6servering af implanterbare humane skeletmuskelafledte celle-mikrob\u00e6rer-kombinationer til brug i klinisk regenerativ medicin"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; admin_label=&#8221;section&#8221; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_row admin_label=&#8221;row&#8221; _builder_version=&#8221;4.21.0&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; width=&#8221;100%&#8221; custom_padding=&#8221;||13px|||&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;4.21.0&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; global_colors_info=&#8221;{}&#8221;]<!-- divi:paragraph --><\/p>\n<p><strong>Simitzi C, Zhang J, Marjsteiner R, Fuller B, Day RM.<\/strong><\/p>\n<p><strong><\/strong><\/p>\n<p>Cytoterapi 12. september 2025.<\/p>\n<p><em>Sammenfatning<\/em><\/p>\n<p>Dette studie unders\u00f8gte, om sm\u00e5, implanterbare kugler med menneskelige muskelceller kan nedfryses og opbevares sikkert til senere medicinsk brug. Disse perler (kaldet mikrob\u00e6rere) er designet til at levere sunde celler til beskadiget v\u00e6v for at hj\u00e6lpe dem med at reparere sig selv. Normalt skal disse celleb\u00e6rende produkter fremstilles friske, hvilket g\u00f8r dem vanskelige at fremstille og distribuere. Forskerne testede forskellige nedfrysnings- og opt\u00f8ningsmetoder og fandt ud af, at muskelcellerne overlevede godt, blev siddende p\u00e5 perlerne og stadig opf\u00f8rte sig normalt efter opt\u00f8ning. Selve perlerne forblev ogs\u00e5 strukturelt sunde. Det betyder, at disse cellebaserede behandlinger i fremtiden kan produceres p\u00e5 forh\u00e5nd, opbevares i en \u201ck\u00f8lek\u00e6de\u201d og leveres til hospitalerne, n\u00e5r der er brug for dem, hvilket g\u00f8r regenerative behandlinger meget mere praktiske og tilg\u00e6ngelige.<\/p>\n<p><em>Abstrakt<\/em><\/p>\n<p>Baggrundsm\u00e5l: Terapier inden for regenerativ medicin omfatter v\u00e6vskonstruktioner, der skal genskabe v\u00e6vs- og organfunktioner. Blandt de forskellige tilgange er implanterbare polymere mikrob\u00e6rere blevet foresl\u00e5et til levering af forankringsafh\u00e6ngige celler til m\u00e5lv\u00e6vssteder. Kombinationer af celler og mikrob\u00e6rere, der produceres som nye l\u00e6gemidler til avanceret terapi, st\u00e5r over for betydelige udfordringer med hensyn til fremstilling og tidsfordeling. I det aktuelle studie har vi unders\u00f8gt muligheden for kryokonservering af kombinationer af humane skeletmuskelafledte celler (SMDC) og implanterbare mikrob\u00e6rere.<\/p>\n<p>Metoder: Eksisterende og nye kryobeskyttende formuleringer kombineret med langsom nedk\u00f8ling blev unders\u00f8gt sammen med hurtige og langsomme opt\u00f8ningsregimer.<\/p>\n<p>Resultater: Under specifikke forhold efter kryopr\u00e6servering og opt\u00f8ning var de fleste SMDC-celler levedygtige og forblev fastgjort til mikrob\u00e6rerne. Desuden var de humane SMDC'ers evne til at differentiere sig til myotuber up\u00e5virket. Kryopr\u00e6serveringsprocessen \u00e6ndrede ikke mikrob\u00e6rernes fysisk-mekaniske egenskaber, hvilket gjorde det muligt for dem at bevare deres prim\u00e6re funktion som et implanterbart cellesubstrat.<\/p>\n<p>Konklusioner: Samlet set baner disse resultater vejen for at bruge koldk\u00e6deproduktforsyning til fremtidige kliniske studier med den implanterbare celle-mikrob\u00e6rerteknologi.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><!-- \/divi:paragraph --><\/p>\n<p>F\u00e5 adgang til hele artiklen her:<\/p>\n<p><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1465324925008424\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1465324925008424<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><!-- \/divi:paragraph -->[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":"<p>Simitzi C, Zhang J, Marjsteiner R, Fuller B, Day RM. Cytotherapy 12th September 2025. Summary This study looked at whether tiny, implantable beads carrying human muscle cells can be safely frozen and stored for later medical use. These beads (called microcarriers) are designed to deliver healthy cells to damaged tissues to help them repair themselves. Normally, these cell-carrying products must be made fresh, which makes them difficult to manufacture and distribute. The researchers tested different freezing and thawing methods and found that the muscle cells survived well, stayed attached to the beads, and still behaved normally after thawing. The beads themselves also remained structurally sound. This means that in the future, these cell-based treatments could be produced in advance, stored in a \u201ccold chain\u201d and delivered to hospitals when needed, making regenerative therapies much more practical and accessible. Abstract Background aims: Regenerative medicine therapies include tissue-engineered constructs to restore tissue and organ function. Among the different approaches, implantable polymeric microcarriers have been proposed for delivery of anchorage-dependent cells to target tissue locations. Cell-microcarrier combinations produced as fresh advanced therapy medicinal products face significant challenges in terms of manufacturing and time distribution. In the current study, we have explored the feasibility [&hellip;]<\/p>","protected":false},"featured_media":31519,"template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"<!-- wp:paragraph -->\n<p>Charlotte Desprez, Davide Danovi, Charles H Knowles and Richard M Day.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>J. Tissue Eng. 2023;14:1\u201318.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p><em>Abstract<\/em><\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Skeletal muscle-derived cells (SMDC) hold tremendous potential for replenishing dysfunctional muscle lost due to disease or trauma. Current therapeutic usage of SMDC relies on harvesting autologous cells from muscle biopsies that are subsequently expanded in vitro before re-implantation into the patient. Heterogeneity can arise from multiple factors including quality of the starting biopsy, age and comorbidity affecting the processed SMDC. Quality attributes intended for clinical use often focus on minimum levels of myogenic cell marker expression. Such approaches do not evaluate the likelihood of SMDC to differentiate and form myofibres when implanted in vivo, which ultimately determines the likelihood of muscle regeneration. Predicting the therapeutic potency of SMDC in vitro prior to implantation is key to developing successful therapeutics in regenerative medicine and reducing implementation costs. Here, we report on the development of a novel SMDC profiling tool to examine populations of cells in vitro derived from different donors. We developed an image-based pipeline to quantify morphological features and extracted cell shape descriptors. We investigated whether these could predict heterogeneity in the formation of myotubes and correlate with the myogenic fusion index. Several of the early cell shape characteristics were found to negatively correlate with the fusion index. These included total area occupied by cells, area shape, bounding box area, compactness, equivalent diameter, minimum ferret diameter, minor axis length and perimeter of SMDC at 24 h after initiating culture. The information extracted with our approach indicates live cell imaging can detect a range of cell phenotypes based on cell-shape alone and preserving cell integrity could be used to predict propensity to form myotubes in vitro and functional tissue in vivo.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Access the full paper here:&nbsp;<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/36949843\/\">https:\/\/pubmed.ncbi.nlm.nih.gov\/36949843\/<\/a><\/p>\n<!-- \/wp:paragraph -->","_et_gb_content_width":"","_coblocks_attr":"","_coblocks_dimensions":"","_coblocks_responsive_height":"","_coblocks_accordion_ie_support":"","_links_to":"","_links_to_target":""},"categories":[43],"class_list":["post-31516","publication","type-publication","status-publish","has-post-thumbnail","hentry","category-publication"],"_links":{"self":[{"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/publication\/31516","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/publication"}],"about":[{"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/types\/publication"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/media\/31519"}],"wp:attachment":[{"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/media?parent=31516"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/amelie-project.eu\/da\/wp-json\/wp\/v2\/categories?post=31516"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}