TY - JOUR
T1 - Microarray with micro- and nano-topographies enables identification of the optimal topography for directing the differentiation of primary murine neural progenitor cells
AU - Moe, Aung Aung Kywe
AU - Suryana, Mona
AU - Marcy, Guillaume
AU - Lim, Sandy Keat
AU - Ankam, Soneela
AU - Goh, Jerome Zhi Wen
AU - Jin, Jing
AU - Teo, Benjamin Kim Kiat
AU - Law, Jaslyn Bee Khuan
AU - Low, Hong Yee
AU - Goh, Eyleen L.K.
AU - Sheetz, Michael P.
AU - Yim, Evelyn K.F.
N1 - Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2012/10/8
Y1 - 2012/10/8
N2 - During development and tissue repair, progenitor cells are guided by both biochemical and biophysical cues of their microenvironment, including topographical signals. The topographical cues have been shown to play an important role in controlling the fate of cells. Systematic investigation of topographical structures with different geometries and sizes under the identical experimental conditions on the same chip will enhance the understanding of the role of shape and size in cell-topography interactions. A simple customizable multi-architecture chip (MARC) array is therefore developed to incorporate, on a single chip, distinct topographies of various architectural complexities, including both isotropic and anisotropic features, in nano- to micrometer dimensions, with different aspect ratios and hierarchical structures. Polydimethylsiloxane (PDMS) replicas of MARC are used to investigate the influence of different geometries and sizes in neural differentiation of primary murine neural progenitor cells (mNPCs). Anisotropic gratings (2 μm gratings, 250 nm gratings) and isotropic 1 μm pillars significantly promote differentiation of mNPCs into neurons, as indicated by expression of β-III-tubulin (59%, 58%, and 58%, respectively, compared to 30% on the control). In contrast, glial differentiation is enhanced on isotropic 2 μm holes and 1 μm pillars. These results illustrate that anisotropic topographies enhance neuronal differentiation while isotropic topographies enhance glial differentiation on the same chip under the same conditions. MARC enables simultaneous cost-effective investigation of multiple topographies, allowing efficient optimization of topographical and biochemical cues to modulate cell differentiation. A multi-architecture chip (MARC) is designed for studying cell-topography interaction more efficiently, based on the simple arithmetic of the patterned area and typical cell area. The MARC is fabricated to incorporate a vast range of topographies with different aspect ratios and different heights to enable rapid high-throughput screening for desired biological applications.
AB - During development and tissue repair, progenitor cells are guided by both biochemical and biophysical cues of their microenvironment, including topographical signals. The topographical cues have been shown to play an important role in controlling the fate of cells. Systematic investigation of topographical structures with different geometries and sizes under the identical experimental conditions on the same chip will enhance the understanding of the role of shape and size in cell-topography interactions. A simple customizable multi-architecture chip (MARC) array is therefore developed to incorporate, on a single chip, distinct topographies of various architectural complexities, including both isotropic and anisotropic features, in nano- to micrometer dimensions, with different aspect ratios and hierarchical structures. Polydimethylsiloxane (PDMS) replicas of MARC are used to investigate the influence of different geometries and sizes in neural differentiation of primary murine neural progenitor cells (mNPCs). Anisotropic gratings (2 μm gratings, 250 nm gratings) and isotropic 1 μm pillars significantly promote differentiation of mNPCs into neurons, as indicated by expression of β-III-tubulin (59%, 58%, and 58%, respectively, compared to 30% on the control). In contrast, glial differentiation is enhanced on isotropic 2 μm holes and 1 μm pillars. These results illustrate that anisotropic topographies enhance neuronal differentiation while isotropic topographies enhance glial differentiation on the same chip under the same conditions. MARC enables simultaneous cost-effective investigation of multiple topographies, allowing efficient optimization of topographical and biochemical cues to modulate cell differentiation. A multi-architecture chip (MARC) is designed for studying cell-topography interaction more efficiently, based on the simple arithmetic of the patterned area and typical cell area. The MARC is fabricated to incorporate a vast range of topographies with different aspect ratios and different heights to enable rapid high-throughput screening for desired biological applications.
KW - biomedical applications
KW - nanoimprinting lithography
KW - neuronal differentiation
KW - tissue engineering
KW - topography screening
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U2 - 10.1002/smll.201200490
DO - 10.1002/smll.201200490
M3 - Article
C2 - 22807278
AN - SCOPUS:84867036829
SN - 1613-6810
VL - 8
SP - 3050
EP - 3061
JO - Small
JF - Small
IS - 19
ER -