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for 48 h, snap-fractured in liquid nitrogen, and sputter-coated with gold before imaging. To assess

               swelling behavior, PMs were blended into the GelMA bioink and crosslinked. After demolding,


               samples were rinsed with PBS (pH 7.4) and blotted to remove excess liquid. The initial dry weight

               was recorded. Samples were immersed in 20 mL PBS at 37°C under shaking (50 rpm). At specified


               intervals (1-24 h), samples were removed, blotted, and weighed. Swelling equilibrium was defined

               as a weight change ≤5% between two consecutive points. The swelling ratio (SR) and moisture


               ratio (MR) were calculated accordingly. Rheological properties were characterized using a dynamic

               shear rheometer Discovery HR-1 (TA, Newcastle, Delaware, USA) with a 50 mm parallel-plate

               geometry (1 mm gap). Both uncrosslinked (PMs/GelMA mixture with photoinitiator, degassed) and


               crosslinked (1 mm thick discs, photocured) samples were tested. Shear viscosity was measured at

                                                  -1
               room temperature from 0 to 1000 s . Temperature-dependent viscosity and moduli (G' and G'')

               were recorded during cooling from 40°C to 0°C at 5°C/min.



               2.5. Construction of Biomimetic Osteochondral Tissue Model


                    The mixture of C-MT or EO-MT and GelMA hydrogel was layer-printed by an extruded 3D

               bioprinter to construct a biomimetic osteochondral tissue model. First, EO-MT composite GelMA


               hydrogel (50 microtissue/mL) was printed in 6-well plates and cured by blue light irradiation for

               10 s. The C-MT composite hydrogel (50 microtissue/mL) was then printed on the EO-MT layer


               and cured by blue light irradiation. Then 1 mL of complete medium was added and placed in an

               incubator.  Meanwhile,  MTs/GelMA  bioink  was  directly  added  into  sterilized  silicone  molds,


               photocrosslinked with  blue light,  demolded, and transferred to  6-well plates  for culture as  the

               casting group. On days 1, 4, and 7, cell viability of both the casting group and the scaffold group


               was assessed using the CCK-8 assay. On day 14, the scaffolds were retrieved, washed with PBS to

               remove residual medium, and their structural integrity was observed. Additionally, on day 14, the




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