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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green <t>=</t> <t>calcein,</t> red = <t>ethidium</t> homodimer). Scale bar = 200 µm.
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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green <t>=</t> <t>calcein,</t> red = <t>ethidium</t> homodimer). Scale bar = 200 µm.
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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green <t>=</t> <t>calcein,</t> red = <t>ethidium</t> homodimer). Scale bar = 200 µm.
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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green <t>=</t> <t>calcein,</t> red = <t>ethidium</t> homodimer). Scale bar = 200 µm.
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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green <t>=</t> <t>calcein,</t> red = <t>ethidium</t> homodimer). Scale bar = 200 µm.
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(A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green = calcein, red = ethidium homodimer). Scale bar = 200 µm.

Journal: bioRxiv

Article Title: Granular Extracellular Matrix (gECM) Hydrogels Enable Distinct Composition and Mechanics Across Tissue Types for Translation

doi: 10.64898/2026.05.06.723348

Figure Lengend Snippet: (A) Skin gECM hydrogel was injected into a microphysiological Emulate chip, with lateral vacuum chambers to apply stretch. Deformation microscopy was performed on confocal images acquired before and after applied stretch to calculate strain maps. (B) Cartilage (left) and bone (right) gECM hydrogels were printed into a microphysiological osteochondral chip that was molded with PDMS. Scale bar = 10 mm. Confocal imaging of tissue-on-chip interface showing pre-stained cartilage (left, red) and bone (right, blue) gECM. Scale bar = 200 µm. Strain maps calculated by deformation microscopy of the cross-section of composite cartilage+bone gECM construct under compression, Eyy (cartilage red, bone blue). (C) Strain maps calculated by deformation microscopy of the cross-section of cartilage gECM under compression plus shear force (Exy), and compression only (Eyy). (D) Bovine chondrocytes cultured with cartilage gECM in a microphysiological chip, with confocal imaging at Day 1 and 14 of culture (green = calcein, red = ethidium homodimer). Scale bar = 200 µm.

Article Snippet: We assessed viability (Calcein AM, Ethidium Homodimer-1; ThermoFisher Invitrogen) via confocal microscopy (Nikon A1R, 10x objective, NA=0.45) at Day 3 and 14.

Techniques: Injection, Microscopy, Imaging, Staining, Construct, Shear, Cell Culture

(A) Bovine chondrocytes cultured on cartilage and (B) murine dermal fibroblasts cultured in skin gECM hydrogels (green = calcein, red = ethidium homodimer, blue = NucBlue). Scale bars = 200 µm. Quantitative PCR showing gene expression (N = 3), fold change to cells cultured on tissue culture plastic (TCP) for 3 days.

Journal: bioRxiv

Article Title: Granular Extracellular Matrix (gECM) Hydrogels Enable Distinct Composition and Mechanics Across Tissue Types for Translation

doi: 10.64898/2026.05.06.723348

Figure Lengend Snippet: (A) Bovine chondrocytes cultured on cartilage and (B) murine dermal fibroblasts cultured in skin gECM hydrogels (green = calcein, red = ethidium homodimer, blue = NucBlue). Scale bars = 200 µm. Quantitative PCR showing gene expression (N = 3), fold change to cells cultured on tissue culture plastic (TCP) for 3 days.

Article Snippet: We assessed viability (Calcein AM, Ethidium Homodimer-1; ThermoFisher Invitrogen) via confocal microscopy (Nikon A1R, 10x objective, NA=0.45) at Day 3 and 14.

Techniques: Cell Culture, Real-time Polymerase Chain Reaction, Gene Expression