| Stem cells |
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Creating a biomimetic environment resembling ECM, enhancing cell adhesion and differentiation.
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Mechanical properties can be tailored to suit the target tissue type.
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Biocompatibility and support for stem cell survival and proliferation.
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CS's biodegradability rate may not align perfectly with stem cell differentiation timelines.
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Risk of immune response or improper integration due to variability in CS's sources and properties.
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Need for controlled delivery of growth factors or biochemical cues to direct differentiation.
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| Chondrocytes |
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Supportive matrix for chondrocyte growth and ECM production (e.g., GAGs, collagen type II).
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Tunable stiffness to simulate native cartilage, aiding repair.
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Biodegradable and biocompatible, support long-term cartilage development.
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Limited in vitro expansion; often requires supplementary bioactive cues.
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Difficulty in maintaining phenotype without biomechanical/biochemical stimuli.
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Long-term stability of mechanical properties may decline.
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| Fibroblasts |
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Enhances fibroblast adhesion, migration, and collagen production, crucial for wound healing.
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Porosity facilitates efficient nutrient exchange and waste removal.
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Surface modification can further enhance fibroblast adhesion.
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Risk of fibrosis or scar tissue formation due to excessive collagen synthesis.
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Mechanical tuning is often required for optimal tissue integration.
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Limited to specific tissue types and ECM components production.
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