Abstract:Fluid shear and other mechanical forces play an important role in the normal biophysical, biochemical, and gene regulatory responses of vertebrate tissue that are reflected in the expression of normal cell differentiation, growth, and function. Despite some promising work reported on the application of the quartz crystal microbalance (QCM) to both prokaryote and eukaryote cells over the last decade, QCM has yet to be successfully applied to cells in culture under conditions of flow-induced shear. In this study… Show more
“…This is in good agreement with numerous publications describing that shear stress can hamper cell adhesion. [36] Unfortunately, there seems to be only one publication investigating the shear stress on cells caused by a QCM under dynamic conditions, [18] making it difficult to estimate its influence on cell adhesion within this system. Experiments with higher pump speeds (and therefore higher shear stress) resulted in significantly lower cell adhesion, a fact, which supports these assumptions (data not shown) and was also described by Jenkins et al [18] Suppressing Cell Adhesion by Grafting PEG Molecules to the Surface A completely different result was obtained when the gold electrodes were modified with (NH 2 PEG 2000 C 11 S) 2 .…”
Section: Detection Of Cell Adhesion Using Non-modified Sensorsmentioning
confidence: 99%
“…[36] Unfortunately, there seems to be only one publication investigating the shear stress on cells caused by a QCM under dynamic conditions, [18] making it difficult to estimate its influence on cell adhesion within this system. Experiments with higher pump speeds (and therefore higher shear stress) resulted in significantly lower cell adhesion, a fact, which supports these assumptions (data not shown) and was also described by Jenkins et al [18] Suppressing Cell Adhesion by Grafting PEG Molecules to the Surface A completely different result was obtained when the gold electrodes were modified with (NH 2 PEG 2000 C 11 S) 2 . In previous investigations, we could show, that the PEG derivatives we synthesized form self-assembled monolayers on gold surfaces, and can significantly reduce the adsorption of proteins due to steric repulsion of PEG, [5,7] an effect which has extensively been described in the literature.…”
Section: Detection Of Cell Adhesion Using Non-modified Sensorsmentioning
confidence: 99%
“…[10,11] However, compared to its use for protein adsorption experiments, only a few studies on cell adhesion using the QCM have been published. [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] The different cell types that have been investigated lead to very different changes in resonance frequencies, depending on the cell seeding density, and of course on the different setups. [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] A significant drawback of all those studies is that most of them were performed under static conditions (except for the study by Jenkins et al [18] ).…”
In this study, the suitability of a flow-through quartz crystal microbalance system for the detection of the adhesion of rMSCs and 3T3-L1 fibroblasts on different surfaces is demonstrated. Frequency shifts for rMSCs of -6.7 mHz x cell(-1) and -2.0 mHz x cell(-1) for 3T3-L1 cells could be detected on non-modified gold sensors, revealing that the frequency shift per cell is comparable to that of a static setup. Modifying the sensor surface with SAMs of thioalkylated omega-amine-terminated PEG derivatives led to cell-adhesion-resistant surfaces. Total frequency shifts of only -20 +/- 7 Hz showed that protein adsorption was also significantly reduced. Attaching 35 pmol x mm(-2) of the GRGDS cell adhesion motif to the SAMs induced specific cell adhesion due to RGD-integrin interactions; the resonance frequency dropped by 3.4 mHz x cell(-1). Furthermore, the kinetics of cell detachment could be determined. The corresponding processes were completed after 10 min for trypsin, and not before 90 min with GRGDS. Moreover, the detectability of cell adhesion was shown to increase after the addition of manganese cations. The total decrease in the resonance frequency was almost 80 Hz in the presence of Mn(2+) (6.4 mHz x cell(-1)). [image: see text] Staining the cytoskeleton of the rMSCs shows that the GRGDS-modified surfaces are almost completely covered with well-spread cells.
“…This is in good agreement with numerous publications describing that shear stress can hamper cell adhesion. [36] Unfortunately, there seems to be only one publication investigating the shear stress on cells caused by a QCM under dynamic conditions, [18] making it difficult to estimate its influence on cell adhesion within this system. Experiments with higher pump speeds (and therefore higher shear stress) resulted in significantly lower cell adhesion, a fact, which supports these assumptions (data not shown) and was also described by Jenkins et al [18] Suppressing Cell Adhesion by Grafting PEG Molecules to the Surface A completely different result was obtained when the gold electrodes were modified with (NH 2 PEG 2000 C 11 S) 2 .…”
Section: Detection Of Cell Adhesion Using Non-modified Sensorsmentioning
confidence: 99%
“…[36] Unfortunately, there seems to be only one publication investigating the shear stress on cells caused by a QCM under dynamic conditions, [18] making it difficult to estimate its influence on cell adhesion within this system. Experiments with higher pump speeds (and therefore higher shear stress) resulted in significantly lower cell adhesion, a fact, which supports these assumptions (data not shown) and was also described by Jenkins et al [18] Suppressing Cell Adhesion by Grafting PEG Molecules to the Surface A completely different result was obtained when the gold electrodes were modified with (NH 2 PEG 2000 C 11 S) 2 . In previous investigations, we could show, that the PEG derivatives we synthesized form self-assembled monolayers on gold surfaces, and can significantly reduce the adsorption of proteins due to steric repulsion of PEG, [5,7] an effect which has extensively been described in the literature.…”
Section: Detection Of Cell Adhesion Using Non-modified Sensorsmentioning
confidence: 99%
“…[10,11] However, compared to its use for protein adsorption experiments, only a few studies on cell adhesion using the QCM have been published. [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] The different cell types that have been investigated lead to very different changes in resonance frequencies, depending on the cell seeding density, and of course on the different setups. [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] A significant drawback of all those studies is that most of them were performed under static conditions (except for the study by Jenkins et al [18] ).…”
In this study, the suitability of a flow-through quartz crystal microbalance system for the detection of the adhesion of rMSCs and 3T3-L1 fibroblasts on different surfaces is demonstrated. Frequency shifts for rMSCs of -6.7 mHz x cell(-1) and -2.0 mHz x cell(-1) for 3T3-L1 cells could be detected on non-modified gold sensors, revealing that the frequency shift per cell is comparable to that of a static setup. Modifying the sensor surface with SAMs of thioalkylated omega-amine-terminated PEG derivatives led to cell-adhesion-resistant surfaces. Total frequency shifts of only -20 +/- 7 Hz showed that protein adsorption was also significantly reduced. Attaching 35 pmol x mm(-2) of the GRGDS cell adhesion motif to the SAMs induced specific cell adhesion due to RGD-integrin interactions; the resonance frequency dropped by 3.4 mHz x cell(-1). Furthermore, the kinetics of cell detachment could be determined. The corresponding processes were completed after 10 min for trypsin, and not before 90 min with GRGDS. Moreover, the detectability of cell adhesion was shown to increase after the addition of manganese cations. The total decrease in the resonance frequency was almost 80 Hz in the presence of Mn(2+) (6.4 mHz x cell(-1)). [image: see text] Staining the cytoskeleton of the rMSCs shows that the GRGDS-modified surfaces are almost completely covered with well-spread cells.
“…The cell layer exhibited periodic, synchronous contractions at a rate of about 1.5 Hz, which was clearly reflected in periodic variations of the resonance frequency and bandwidth, and which could be modulated by stimulating drugs such as isoproterenol. Cell-based studies have also been extended to monitor shear-induced senescence in human embryonic kidney cells in culture under conditions of flow-induced shear (Jenkins et al, 2004b), and vesicle release and retrieval (Cans et al, 2001). In the latter study, increasing potassium concentration in the media was shown to stimulate exocytosis, whilst the endocytosis was spontaneous.…”
Section: Cellular Responses To Exogenous Stimulimentioning
The widespread exploitation of biosensors in the analysis of molecular recognition has its origins in the mid-1990s following the release of commercial systems based on surface plasmon resonance (SPR). More recently, platforms based on piezoelectric acoustic sensors (principally 'bulk acoustic wave' (BAW), 'thickness shear mode' (TSM) sensors or 'quartz crystal microbalances' (QCM)), have been released that are driving the publication of a large number of papers analysing binding specificities, affinities, kinetics and conformational changes associated with a molecular recognition event. This article highlights salient theoretical and practical aspects of the technologies that underpin acoustic analysis, then reviews exemplary papers in key application areas involving small molecular weight ligands, carbohydrates, proteins, nucleic acids, viruses, bacteria, cells and lipidic and polymeric interfaces. Key differentiators between optical and acoustic sensing modalities are also reviewed.
“…Of the measurement methods, surface plasmon resonance (SPR) (Baac et al, 2006;Hodin et al, 2007;Jacquemart et al, 2008;Suenaga et al, 2003;Wolf et al, 2005) and quartz crystal microbalance (QCM) (Hodin et al, 2007;Jenkins et al, 2004;Nakano et al, 2007;Rawle et al, 2007;Sota et al, 2002) are very popular. For these measurements, some types of sensor chips are commercially available, although there are in general numerous immobilization methods (Rusmin et al, 2007).…”
The photo-immobilization technique is useful for immobilization of various biomolecules on assorted material surfaces, independent of the organic functional groups that may be present. Here, we report a convenient new photo-immobilization technique that was developed by combining a nonbiofouling polymer containing polyethylene glycol and a photoreactive crosslinker for surface plasmon resonance (SPR) and quartz crystal microbalance (QCM) measurements. By this method, nonspecific interactions were reduced and various types of molecules, bovine serum albumin, heparin, dsDNA, phosphatidylserine, Tobacco Mosaic Virus, and norfloxacine, were immobilized on an alkane thiol-modified gold surface by a single method. The interactions of photo-immobilized biomolecules and their corresponding antibodies were investigated by SPR and QCM. In addition, SPR imaging was possible using the present method.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.