Cell-matrix and cell-cell interactions of human gingival fibroblasts on three-dimensional nanofibrous gelatin scaffolds

2012 ◽  
Vol 8 (11) ◽  
pp. 862-873 ◽  
Author(s):  
Ashneet Sachar ◽  
T. Amanda Strom ◽  
Symone San Miguel ◽  
Maria J. Serrano ◽  
Kathy K. H. Svoboda ◽  
...  
SciVee ◽  
2012 ◽  
Author(s):  
Xinbo Li ◽  
Diala Abu-Hassan ◽  
Janice Vranka ◽  
John Bradley ◽  
Ted Acott ◽  
...  

2016 ◽  
Vol 13 (123) ◽  
pp. 20160613 ◽  
Author(s):  
Sebastian V. Hadjiantoniou ◽  
David Sean ◽  
Maxime Ignacio ◽  
Michel Godin ◽  
Gary W. Slater ◽  
...  

During embryogenesis, the spherical inner cell mass (ICM) proliferates in the confined environment of a blastocyst. Embryonic stem cells (ESCs) are derived from the ICM, and mimicking embryogenesis in vitro , mouse ESCs (mESCs) are often cultured in hanging droplets. This promotes the formation of a spheroid as the cells sediment and aggregate owing to increased physical confinement and cell–cell interactions. In contrast, mESCs form two-dimensional monolayers on flat substrates and it remains unclear if the difference in organization is owing to a lack of physical confinement or increased cell–substrate versus cell–cell interactions. Employing microfabricated substrates, we demonstrate that a single geometric degree of physical confinement on a surface can also initiate spherogenesis. Experiment and computation reveal that a balance between cell–cell and cell–substrate interactions finely controls the morphology and organization of mESC aggregates. Physical confinement is thus an important regulatory cue in the three-dimensional organization and morphogenesis of developing cells.


2014 ◽  
Vol 11 (99) ◽  
pp. 20140631 ◽  
Author(s):  
Alexander Gord ◽  
William R. Holmes ◽  
Xing Dai ◽  
Qing Nie

Skin is a complex organ tasked with, among other functions, protecting the body from the outside world. Its outermost protective layer, the epidermis, is comprised of multiple cell layers that are derived from a single-layered ectoderm during development. Using a new stochastic, multi-scale computational modelling framework, the anisotropic subcellular element method, we investigate the role of cell morphology and biophysical cell–cell interactions in the formation of this layered structure. This three-dimensional framework describes interactions between collections of hundreds to thousands of cells and (i) accounts for intracellular structure and morphology, (ii) easily incorporates complex cell–cell interactions and (iii) can be efficiently implemented on parallel architectures. We use this approach to construct a model of the developing epidermis that accounts for the internal polarity of ectodermal cells and their columnar morphology. Using this model, we show that cell detachment, which has been previously suggested to have a role in this process, leads to unpredictable, randomized stratification and that this cannot be abrogated by adjustment of cell–cell adhesion interaction strength. Polarized distribution of cell adhesion proteins, motivated by epithelial polarization, can however eliminate this detachment, and in conjunction with asymmetric cell division lead to robust and predictable development.


PLoS ONE ◽  
2014 ◽  
Vol 9 (3) ◽  
pp. e90715 ◽  
Author(s):  
Wesley Mah ◽  
Guoqiao Jiang ◽  
Dylan Olver ◽  
Godwin Cheung ◽  
Ben Kim ◽  
...  

1997 ◽  
Vol 272 (52) ◽  
pp. 33245-33254 ◽  
Author(s):  
Masanobu Komatsu ◽  
Coralie A. Carothers Carraway ◽  
Nevis L. Fregien ◽  
Kermit L. Carraway

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