{"id":{"repo_id":"bradford","oai_identifier":"oai:bradscholars.brad.ac.uk:10454/20543"},"canonical_url":"https://search.dev.ndltd.org/etd/bradford/oai:bradscholars.brad.ac.uk:10454/20543","repository":{"repo_id":"bradford","name":"University of Bradford","base_url":"https://bradscholars.brad.ac.uk/oai/request"},"display":{"title":"Modulation of human adipose-derived stem cells and dermal fibroblasts in co-cultures by activation of the IL-6 trans-signalling pathway via the soluble IL-6Rα receptor","abstract":"Interleukin-6 (IL-6), a major wound healing cytokine, has rare, versatile agonistic effects, due to dual pro and anti-inflammatory roles depending on the intracellular signalling pathway. The aim was to evaluate the relationship between human dermal fibroblasts (DF), human adipose-derived stem cells (ADSC), IL-6 and activation of the IL-6 trans-signalling pathway under four different cell culture conditions. The two cell types were co-cultured to assess cell migration when pre-treated with the soluble human IL-6Rα receptor (rhIL-6Rα). In addition, secreted cytokine levels (TGFβ1, TGFβ3 and VEGF) and biomarker expression (TGF β1RII, SMAD2/3, SMAD 1/5/9 and SMA) were quantitated. Although both cell types secreted IL-6, ADSC basal levels were 100-fold that of DF. Both cell types expressed CD130 (gp130) signalling transductor but were negative for the membrane-bound CD126 receptor required for the classical IL-6 signalling pathway. Following IL-6 trans-signalling pathway activation with rhIL-6Rα, ADSC migrated predominantly, while DF acted more as attractants. Moreover, the overall secretion of TGFβ3 and VEGF, and the ratio of TGFβ3/TGFβ1 showed similar variations which suggested they increased, although not statistically significant and were maintained at 72h, but only in co-cultures where the ADSC were pre-treated. When cells were pre-treated with rhIL-6Rα, the overall expression of TGFβRII and SMAD2/3 increased suggesting crosstalk between TGFβ1 and IL-6. In summary, these results suggest that activation of the IL-6 trans-signalling pathway modulates ADSC plasticity impacting on migration. Thus, further research is required to assess the use of ADSC in concurrence with manipulation of the IL-6 signalling pathway in wound management.","abstract_html":"Interleukin-6 (IL-6), a major wound healing cytokine, has rare, versatile agonistic effects, due to dual pro and anti-inflammatory roles depending on the intracellular signalling pathway. The aim was to evaluate the relationship between human dermal fibroblasts (DF), human adipose-derived stem cells (ADSC), IL-6 and activation of the IL-6 trans-signalling pathway under four different cell culture conditions. The two cell types were co-cultured to assess cell migration when pre-treated with the soluble human IL-6Rα receptor (rhIL-6Rα). In addition, secreted cytokine levels (TGFβ1, TGFβ3 and VEGF) and biomarker expression (TGF β1RII, SMAD2/3, SMAD 1/5/9 and SMA) were quantitated. Although both cell types secreted IL-6, ADSC basal levels were 100-fold that of DF. Both cell types expressed CD130 (gp130) signalling transductor but were negative for the membrane-bound CD126 receptor required for the classical IL-6 signalling pathway. Following IL-6 trans-signalling pathway activation with rhIL-6Rα, ADSC migrated predominantly, while DF acted more as attractants. Moreover, the overall secretion of TGFβ3 and VEGF, and the ratio of TGFβ3/TGFβ1 showed similar variations which suggested they increased, although not statistically significant and were maintained at 72h, but only in co-cultures where the ADSC were pre-treated. When cells were pre-treated with rhIL-6Rα, the overall expression of TGFβRII and SMAD2/3 increased suggesting crosstalk between TGFβ1 and IL-6. In summary, these results suggest that activation of the IL-6 trans-signalling pathway modulates ADSC plasticity impacting on migration. Thus, further research is required to assess the use of ADSC in concurrence with manipulation of the IL-6 signalling pathway in wound management.","abstract_has_math":false,"creators":["Chelmuș, Alina"],"institution":"University of Bradford","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Thornton, M. Julie","Riches-Suman, Kirsten"],"committee_chairs":[],"committee_members":[],"year":null,"date_issued":"","date_published":null,"updated_at":"2026-07-24T01:14:55Z","subjects":["Wound healing","Soluble IL-6Rα receptor","Adipose-derived stem cells","Dermal fibroblasts","Migration","IL-6 trans-signalling pathway","Interleukin-6 (IL-6)"],"languages":["en"],"rights":["<a rel=\"license\" href=\"http://creativecommons.org/licenses/by-nc-nd/3.0/\"><img alt=\"Creative Commons License\" style=\"border-width:0\" src=\"http://i.creativecommons.org/l/by-nc-nd/3.0/88x31.png\" /></a><br />The University of Bradford theses are licenced under a <a rel=\"license\" href=\"http://creativecommons.org/licenses/by-nc-nd/3.0/\">Creative Commons Licence</a>."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://bradscholars.brad.ac.uk/handle/10454/20543","outbound_label":"Repository record","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Thornton, M. 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The aim was to evaluate the relationship between human dermal fibroblasts (DF), human adipose-derived stem cells (ADSC), IL-6 and activation of the IL-6 trans-signalling pathway under four different cell culture conditions. The two cell types were co-cultured to assess cell migration when pre-treated with the soluble human IL-6Rα receptor (rhIL-6Rα). In addition, secreted cytokine levels (TGFβ1, TGFβ3 and VEGF) and biomarker expression (TGF β1RII, SMAD2/3, SMAD 1/5/9 and SMA) were quantitated. Although both cell types secreted IL-6, ADSC basal levels were 100-fold that of DF. Both cell types expressed CD130 (gp130) signalling transductor but were negative for the membrane-bound CD126 receptor required for the classical IL-6 signalling pathway. Following IL-6 trans-signalling pathway activation with rhIL-6Rα, ADSC migrated predominantly, while DF acted more as attractants. Moreover, the overall secretion of TGFβ3 and VEGF, and the ratio of TGFβ3/TGFβ1 showed similar variations which suggested they increased, although not statistically significant and were maintained at 72h, but only in co-cultures where the ADSC were pre-treated. When cells were pre-treated with rhIL-6Rα, the overall expression of TGFβRII and SMAD2/3 increased suggesting crosstalk between TGFβ1 and IL-6. In summary, these results suggest that activation of the IL-6 trans-signalling pathway modulates ADSC plasticity impacting on migration. Thus, further research is required to assess the use of ADSC in concurrence with manipulation of the IL-6 signalling pathway in wound management."]},{"key":"dc:title","label":"Title","values":["Modulation of human adipose-derived stem cells and dermal fibroblasts in co-cultures by activation of the IL-6 trans-signalling pathway via the soluble IL-6Rα receptor"]}]}],"canonical_facts":{"dc:contributor.advisor":["Thornton, M. Julie","Riches-Suman, Kirsten"],"dc:creator":["Chelmuș, Alina"],"dc:date.accessioned":["2025-07-30T15:46:49Z"],"dc:date.available":["2025-07-30T15:46:49Z"],"dc:description.abstract":["Interleukin-6 (IL-6), a major wound healing cytokine, has rare, versatile agonistic effects, due to dual pro and anti-inflammatory roles depending on the intracellular signalling pathway. The aim was to evaluate the relationship between human dermal fibroblasts (DF), human adipose-derived stem cells (ADSC), IL-6 and activation of the IL-6 trans-signalling pathway under four different cell culture conditions. The two cell types were co-cultured to assess cell migration when pre-treated with the soluble human IL-6Rα receptor (rhIL-6Rα). In addition, secreted cytokine levels (TGFβ1, TGFβ3 and VEGF) and biomarker expression (TGF β1RII, SMAD2/3, SMAD 1/5/9 and SMA) were quantitated. Although both cell types secreted IL-6, ADSC basal levels were 100-fold that of DF. Both cell types expressed CD130 (gp130) signalling transductor but were negative for the membrane-bound CD126 receptor required for the classical IL-6 signalling pathway. Following IL-6 trans-signalling pathway activation with rhIL-6Rα, ADSC migrated predominantly, while DF acted more as attractants. Moreover, the overall secretion of TGFβ3 and VEGF, and the ratio of TGFβ3/TGFβ1 showed similar variations which suggested they increased, although not statistically significant and were maintained at 72h, but only in co-cultures where the ADSC were pre-treated. When cells were pre-treated with rhIL-6Rα, the overall expression of TGFβRII and SMAD2/3 increased suggesting crosstalk between TGFβ1 and IL-6. In summary, these results suggest that activation of the IL-6 trans-signalling pathway modulates ADSC plasticity impacting on migration. Thus, further research is required to assess the use of ADSC in concurrence with manipulation of the IL-6 signalling pathway in wound management."],"dc:identifier.uri":["https://bradscholars.brad.ac.uk/handle/10454/20543"],"dc:language.iso":["en"],"dc:publisher.department":["School of Chemistry and Biosciences. Faculty of Life Sciences"],"dc:publisher.institution":["University of Bradford"],"dc:rights":["<a rel=\"license\" href=\"http://creativecommons.org/licenses/by-nc-nd/3.0/\"><img alt=\"Creative Commons License\" style=\"border-width:0\" src=\"http://i.creativecommons.org/l/by-nc-nd/3.0/88x31.png\" /></a><br />The University of Bradford theses are licenced under a <a rel=\"license\" href=\"http://creativecommons.org/licenses/by-nc-nd/3.0/\">Creative Commons Licence</a>."],"dc:subject":["Wound healing","Soluble IL-6Rα receptor","Adipose-derived stem cells","Dermal fibroblasts","Migration","IL-6 trans-signalling pathway","Interleukin-6 (IL-6)"],"dc:title":["Modulation of human adipose-derived stem cells and dermal fibroblasts in co-cultures by activation of the IL-6 trans-signalling pathway via the soluble IL-6Rα receptor"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["research masters"],"dc:type.qualificationname":["MPhil"]},"updated_at":"2026-07-24T01:14:55Z"}