2015
DOI: 10.1016/j.biomaterials.2015.08.016
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Cell type-specific adaptation of cellular and nuclear volume in micro-engineered 3D environments

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Cited by 46 publications
(32 citation statements)
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“…Although the proliferation and adhesion were similar to conventional 2D culture conditions, the cells largely differed with respect to their morphology. Strikingly, fibroblasts, but not epithelial cells, almost doubled their cellular volume when cultured in 3D . This is consistent to their in vivo origin, where fibroblasts grow in a complex 3D environment whereas epithelial cells form a planar tissue.…”
Section: Direct Laser Writing For Cell Culturesupporting
confidence: 77%
“…Although the proliferation and adhesion were similar to conventional 2D culture conditions, the cells largely differed with respect to their morphology. Strikingly, fibroblasts, but not epithelial cells, almost doubled their cellular volume when cultured in 3D . This is consistent to their in vivo origin, where fibroblasts grow in a complex 3D environment whereas epithelial cells form a planar tissue.…”
Section: Direct Laser Writing For Cell Culturesupporting
confidence: 77%
“…For instance, the volume‐sensitive Cl − channel has been found to play an important role in both cell volume regulation (Lee et al, ; Shimizu, ) and cisplatin resistance of human cancer cells. In addition, accumulating evidence has shown some other influence factors on cell volume (Bush, Hodkinson, Hamilton, & Hall, ; Greiner et al, ; Marino & La Spada, ; Turunen et al, ). For instance, the volume of chondrocytes reduces up to 30% under compressive force loading (Bush et al, ).…”
Section: Introductionmentioning
confidence: 99%
“…[8][9][10] Im letzten Jahrzehnt hat sich hier das DLWals ein leistungsfähiges Verfahren erwiesen, um zelluläre 3D-Mikroumgebungen mit wohldefinierter Geometrie herzustellen. In einem Großteil dieser Studien wurden Gerüststrukturen, bestehend aus einem einzelnen Photolack mit einer homogenen Oberflächenbeschichtung aus Biomolekülen, verwendet, um Zellwachstum, [11,12] Zelladhäsion, [13,14] Zellmigration [15,16] oder Stammzelldifferenzierung [17] in definierten 3D-Mikroumgebungen zu untersuchen. In letzter Zeit sind mehrere exzellente Übersichtsartikel über die relevante Literatur erschienen und wir verweisen auf die dort zitierten Arbeiten.…”
Section: Zellkulturanwendungenunclassified