Formation of Wrinkle Patterns on Porous Elastomeric Membrane and Their Fabrication of Hierarchical Architectures

2008 ◽  
Vol 1129 ◽  
Author(s):  
Yue Cui ◽  
Shu Yang

AbstractWe report the formation of wrinkle patterns on porous elastomeric membrane and their fabrication of hierarchical architectures through mechanical stretching and replica molding. The technique builds upon a buckling instability of a stiff layer supported by a porous elastomeric membrane which was induced by surface plasma oxidation of the pre-stretched porous elastomer followed by removal of the applied mechanical strain to form wrinkle patterns, and replica molding of the deformed features on the porous membrane into epoxy to form hierarchical architectures through casting the UV-curable epoxy prepolymer and UV curing. We find that due to the existence of micropores on the membrane, the formation of wrinkle patterns is different from that formed on a continuous elastomeric film, and by varying the applied mechanical stretching strain condition and plasma oxidation condition, the wrinkle patterns could be either confined by the micropores on the membrane to exhibit a wavelength equal to its pitch or form wrinkles with much large wavelength compared with that formed on a continuous elastomeric film. Therefore, the micropillar arrays fabricated by replica molding could stand on different types of wrinkle patterns to form different hierarchical architectures. The method we illustrate here offers a simple and cost-effective approach to fabricate various hierarchical structures, and provides possibilities for potential applications in various fields, such as microfluidics, micro- and nanofabrication of complex structures, crystal formation, cell attachment, superhydrophobicity and dry adhesion.

2016 ◽  
Vol 25 (12) ◽  
pp. 2213-2220 ◽  
Author(s):  
Deepak Kumar ◽  
Alex Lyness ◽  
Irini Gerges ◽  
Christina Lenardi ◽  
Nicholas R. Forsyth ◽  
...  

Nucleus pulposus (NP) tissue damage can induce detrimental mechanical strain on the biomechanical performance of intervertebral discs (IVDs), causing subsequent disc degeneration. A novel, photocurable, injectable, synthetic polymer hydrogel (pHEMA-co-APMA grafted with PAA) has already demonstrated success in encapsulating and differentiating human mesenchymal stem cells (hMSCs) toward an NP phenotype during hypoxic conditions. After demonstration of promising results in our previous work, in this study we have further investigated the inclusion of mechanical stimulation and its impact on hMSC differentiation toward an NP phenotype through the characterization of matrix markers such as SOX-9, aggrecan, and collagen II. Furthermore, investigations were undertaken in order to approximate delivery parameters for an injection delivery device, which could be used to transport hMSCs suspended in hydrogel into the IVD. hMSC-laden hydrogel solutions were injected through various needle gauge sizes in order to determine its impact on postinjection cell viability and IVD tissue penetration. Interpretation of these data informed the design of a potential minimally invasive injection device, which could successfully inject hMSCs encapsulated in a UV-curable polymer into NP, prior to photo-cross-linking in situ.


2017 ◽  
Author(s):  
Ben K. A. Nelemans ◽  
Manuel Schmitz ◽  
Hannan Tahir ◽  
Roeland M. H. Merks ◽  
Theodoor H. Smit

AbstractPhysical cues, experienced during early embryonic development, can influence species-specific vertebral numbers. Here we show that mechanical stretching of live chicken embryos can induce the formation of additional somites and thereby modify early segmental patterning. Stretching deforms the somites, and results in a cellular reorganization that forms stable daughter somites. Cells from the somite core thereby undergo mesenchymal-to-epithelial transitions (MET), thus meeting the geometrical demand for more border cells. Using a Cellular Potts Model, we suggest that this MET occurs through lateral induction by the existing epithelial cells. Our results indicate that self-organizing properties of the somitic mesoderm generate phenotypic plasticity that allows it to cope with variations in the mechanical environment. This plasticity may provide a novel mechanism for explaining how vertebral numbers in species may have increased during evolution. Additionally, by preventing the formation of transitional vertebrae, these self-organization qualities of somites may be selectively advantageous.


Author(s):  
Szu-Yuan Chou ◽  
Chao-Min Cheng ◽  
Yi-Wen Lin ◽  
Chih-Cheng Chen ◽  
Philip R. LeDuc

Mechanical stimulation affects the functioning and outgrowth of neurons and has the potential capacity for regeneration. Mechanoreceptors in sensory neurons act as a conduit to respond to pain and touch while neurites experience mechanical stimulation during the process of animal growth. To understand mechanotransduction in neural outgrowth, we used a custom fabricated device to investigate the effects of static mechanical stretching while examining molecular connections such as advillin and actin. Our results have the potential of providing greater understanding of mechanotransduction in neuroblasts, as well as providing insight into mechanical approaches that might be used in increasing neural outgrowth.


Coatings ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 622
Author(s):  
Fei Sun ◽  
Shao-Jie Li ◽  
Xin-Chang Li ◽  
Lei Wang ◽  
De-Chun Ba ◽  
...  

Plasma oxidation could produce an oxidized surface, resulting in a graded TiO2−x film layer and significantly improving dental implant hydrophilicity and biocompatibility. Unfortunately, these features are gradually lost by the influence of the environment. In this study, alkali storage was used to improve these characteristics at room temperature. Titanium samples were divided into sandblasting acid-etching (SLA), oxidation (SLA samples that were oxidized), and storage (SLA samples that were oxidized and stored in 0.1 mol/L NaOH solution) groups. We measured the surface properties of each group, including the roughness, chemical composition, and hydrophilicity of these materials. We investigated the effects of titanium storage on cell responses, including cell attachment, proliferation, differentiation. We also investigated the osseointegration of the stored titanium implants. The results showed that the storage process maintains the superhydrophilic properties of oxidation treatment. Oxidized samples promoted cell responses. The descending order of biocompatibility was storage > oxidation > SLA. Furthermore, oxidation and alkali storage had significant effects on bone growth at the early stage of the implant. These results suggested that alkali storage can suitably maintain the surface characteristics of plasma oxidation, and the combination of oxidation and storage treatment can improve the primary implant stability.


1999 ◽  
Vol 10 (1) ◽  
pp. 79-98 ◽  
Author(s):  
B. Ganss ◽  
R.H. Kim ◽  
J. Sodek

The search for a protein nucleator of hydroxyapatite crystal formation has been a focus for the isolation and characterization of the major non-collagenous proteins in bone. Of the proteins characterized to date, bone sialoprotein (BSP) has emerged as the only bona fide candidate for nucleation. BSP is a highly glycosylated and sulphated phosphoprotein that is found almost exclusively in mineralized connective tissues. Characteristically, polyglutamic acid and arginine-glycine-aspartate (RGD) motifs with the ability to bind hydroxyapatite and cell-surface integrins, respectively, have been conserved in the protein sequence. Expression of the BSP gene, which is induced in newly formed osteoblasts, is up-regulated by hormones and cytokines that promote bone formation and down-regulated by factors that suppress bone formation. Thus, BSP has the biophysical and chemical properties of a nucleator, and its temporo-spatial expression coincides with de novo mineralization in bone and cementum. Moreover, BSP has been associated with mineral crystal formation in several pathologies, including breast carcinomas. However, the ability of BSP to mediate cell attachment and to signal through the RGD motif points to alternate functions for BSP which need further investigation. In combination, the hydroxyapatite-binding polyglutamic acid sequences and the RGD provide bi-functional entities through which BSP may mediate the targeting and attachment of normal and metastasizing cells to the bone surface.


2006 ◽  
Vol 290 (2) ◽  
pp. L343-L350 ◽  
Author(s):  
Juan Sanchez-Esteban ◽  
Yulian Wang ◽  
Edward J. Filardo ◽  
Lewis P. Rubin ◽  
Donald E. Ingber

Mechanical forces regulate lung maturation in the fetus by promoting type II epithelial differentiation. However, the cell surface receptors that transduce these mechanical cues into cellular responses remain largely unknown. When distal lung type II epithelial cells isolated from embryonic day 19 rat fetuses were cultured on flexible plates coated with laminin, fibronectin, vitronectin, collagen, or elastin and exposed to a level of mechanical strain (5%) similar to that observed in utero, transmembrane signaling responses were induced under all conditions, as measured by ERK activation. However, mechanical stress maximally increased expression of the type II cell differentiation marker surfactant protein C when cells were cultured on laminin substrates. Strain-induced alveolar epithelial differentiation was inhibited by interfering with cell binding to laminin using soluble laminin peptides (IKVIV or YIGSR) or blocking antibodies against integrin β1, α3, or α6. Additional studies were carried out with substrates coated directly with different nonactivating anti-integrin antibodies. Blocking integrin β1 and α6 binding sites inhibited both cell adhesion and differentiation, whereas inhibition of α3 prevented differentiation without altering cell attachment. These data demonstrate that various integrins contribute to mechanical control of type II lung epithelial cell differentiation on laminin substrates. However, they may act via distinct mechanisms, including some that are independent of their cell anchoring role.


Author(s):  
Charles TurnbiLL ◽  
Delbert E. Philpott

The advent of the scanning electron microscope (SCEM) has renewed interest in preparing specimens by avoiding the forces of surface tension. The present method of freeze drying by Boyde and Barger (1969) and Small and Marszalek (1969) does prevent surface tension but ice crystal formation and time required for pumping out the specimen to dryness has discouraged us. We believe an attractive alternative to freeze drying is the critical point method originated by Anderson (1951; for electron microscopy. He avoided surface tension effects during drying by first exchanging the specimen water with alcohol, amy L acetate and then with carbon dioxide. He then selected a specific temperature (36.5°C) and pressure (72 Atm.) at which carbon dioxide would pass from the liquid to the gaseous phase without the effect of surface tension This combination of temperature and, pressure is known as the "critical point" of the Liquid.


Author(s):  
Etienne de Harven ◽  
Nina Lampen

Samples of heparinized blood, or bone marrow aspirates, or cell suspensions prepared from biopsied tissues (nodes, spleen, etc. ) are routinely prepared, after Ficoll-Hypaque concentration of the mononuclear leucocytes, for scanning electron microscopy. One drop of the cell suspension is placed in a moist chamber on a poly-l-lysine pretreated plastic coverslip (Mazia et al., J. Cell Biol. 66:198-199, 1975) and fifteen minutes allowed for cell attachment. Fixation, started in 2. 5% glutaraldehyde in culture medium at room temperature for 30 minutes, is continued in the same fixative at 4°C overnight or longer. Ethanol dehydration is immediately followed by drying at the critical point of CO2 or of Freon 13. An efficient alternative method for ethanol dehydrated cells is to dry the cells at low temperature (-75°C) under vacuum (10-2 Torr) for 30 minutes in an Edwards-Pearse freeze-dryer (de Harven et al., SEM/IITRI/1977, 519-524). This is preceded by fast quenching in supercooled ethanol (between -90 and -100°C).


Author(s):  
B. Craig ◽  
L. Hawkey ◽  
A. LeFurgey

Ultra-rapid freezing followed by cryoultramicrotomy is essential for the preservation of diffusible elements in situ within cells prior to scanning transmission electron microscopy and quantitative energy dispersive x-ray microanalysis. For cells or tissue fragments in suspension and for monolayer cell cultures, propane jet freezing provides cooling rates greater than 30,000°C/sec with regions up to 40μm in thickness free of significant ice crystal formation. While this method of freezing has frequently been applied prior to freeze fracture or freeze substitution, it has not been widely utilized prior to cryoultramicrotomy and subsequent x-ray microanalytical studies. This report describes methods devised in our laboratory for cryosectioning of propane jet frozen kidney proximal tubule suspensions and cultured embryonic chick heart cells, in particular a new technique for mounting frozen suspension specimens for sectioning. The techniques utilize the same specimen supports and sample holders as those used for freeze fracture and freeze substitution and should be generally applicable to any cell suspension or culture preparation.


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