scholarly journals Study of FRSN cells migration under the conditions of continuous low flow

Author(s):  
А.А. Московцев ◽  
Д.В. Колесов ◽  
А.Н. Мыльникова ◽  
А.А. Кубатиев

Поток жидкости оказывает значительное влияние на морфофункциональное состояние большинства клеток в организме. Это может проявляться в миграции клеток под действием сдвиговой деформации или градиента питательных веществ. Мезенхимные стволовые фибробластоподобные клетки FRSN были культивированы в условиях воздействия постоянного потока жидкости в микрофлюидном чипе. Проведены исследования миграции клеток на разных стадиях адгезии под действием потока в различных областях чипа. Обнаружены значительные перемещения клеток в режиме «stick-slip» вдоль направления потока. The fluid flow exerts a significant effect on most cells in the body. This effect can involve cell migration under the action of shear stress or nutrient gradient. FRSN mesenchymal stem cells were cultured under the action of a constant fluid flow of low intensity in a microfluidic chip. The study of cell migration at different stages of adhesion was performed under the action of flow in different areas of the chip. Significant cell movements in a stick-slip mode along the flow direction were observed.

1993 ◽  
Vol 104 (4) ◽  
pp. 1145-1153 ◽  
Author(s):  
D.E. Coan ◽  
A.R. Wechezak ◽  
R.F. Viggers ◽  
L.R. Sauvage

Despite substantial evidence to suggest that directed cell migration is dependent upon positioning of the Golgi apparatus (GA) and the microtubule organizing center (MTOC), some controversy exists about whether such a relationship is relevant to endothelial cells under flow. The present study was undertaken to provide an indepth investigation of the relationship between shear stress, GA/MTOC localization, cell migration and nuclear position. Bovine carotid endothelial cells were exposed to 22 or 88 dynes/cm2 for 0.5, 2, 8 or 24 h, and localization of their GA/MTOCs was determined relative to the direction of flow. In no-flow control specimens, (0, 0.5, 2, 8 and 24 h) there was no change in the equally distributed GA/MTOCs. In contrast, during the first 8 h at 88 dynes/cm2 and by 2 h at 22 dynes/cm2 there was a significant increase in the number of cells with GA/MTOCs localized upstream to flow direction. The effect was temporary, however, and by 24 h there was no significant difference between the no-flow, 22 and 88 dynes/cm2 specimens. Analysis of GA/MTOC localization with respect to the direction of cell migration determined that 72.5% of no-flow cells possessed GA/MTOCs localized to the sides of nuclei nearest the direction of migration. In contrast, 64% of the specimens shear stressed over the same time period had GA/MTOCs localized to the sides of nuclei opposite the direction of migration. These results suggest that positioning of the GA/MTOC in endothelial cells is not dependent completely upon the direction of migration.(ABSTRACT TRUNCATED AT 250 WORDS)


2020 ◽  
Vol 15 (5) ◽  
pp. 462-472 ◽  
Author(s):  
Abdollah Amini ◽  
Sufan Chien ◽  
Mohammad Bayat

Objective: This is a systematic review of the effects of low-intensity pulsed ultrasound (LIPUS) on stem cell differentiation. Background Data: Recent studies have investigated several types of stem cells from different sources in the body. These stem cells should strictly be certified and promoted for cell therapies before being used in medical applications. LIPUS has been used extensively in treatment centers and in research to promote stem cell differentiation, function, and proliferation. Materials and Methods: The databases of PubMed, Google Scholar, and Scopus were searched for abstracts and full-text scientific papers published from 1989-2019 that reported the application of LIPUS on stem cell differentiation. Related English language articles were found using the following defined keywords: low-intensity pulsed ultrasound, stem cell, differentiation. Criteria for inclusion in the review were: LIPUS with frequencies of 1–3 MHz and pulsed ultrasound intensity of <500 mW/cm2. Duration, exposure time, and cell sources were taken into consideration. Results: Fifty-two articles were selected based on the inclusion criteria. Most articles demonstrated that the application of LIPUS had positive effects on stem cell differentiation. However, some authors recommended that LIPUS combined with other physical therapy aides was more effective in stem cell differentiation. Conclusions: LIPUS significantly increases the level of stem cell differentiation in cells derived mainly from bone marrow mesenchymal stem cells. There is a need for further studies to analyze the effect of LIPUS on cells derived from other sources, particularly adipose tissue-derived mesenchymal stem cells, for treating hard diseases, such as osteoporosis and diabetic foot ulcer. Due to a lack of reporting on standard LIPUS parameters in the field, more experiments comparing the protocols for standardization of LIPUS parameters are needed to establish the best protocol, which would allow for the best results.


2014 ◽  
Vol 8 (5) ◽  
pp. 052008 ◽  
Author(s):  
Xinghua Gao ◽  
Xu Zhang ◽  
Hui Xu ◽  
Bingpu Zhou ◽  
Weijia Wen ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Ping Wang

Discrete element method (DEM) is used to produce dense and fixed porous media with rigid mono spheres. Lattice Boltzmann method (LBM) is adopted to simulate the fluid flow in interval of dense spheres. To simulating the same physical problem, the permeability is obtained with different lattice number. We verify that the permeability is irrelevant to the body force and the media length along flow direction. The relationships between permeability, tortuosity and porosity, and sphere radius are researched, and the results are compared with those reported by other authors. The obtained results indicate that LBM is suited to fluid flow simulation of porous media due to its inherent theoretical advantages. The radius of sphere should have ten lattices at least and the media length along flow direction should be more than twenty radii. The force has no effect on the coefficient of permeability with the limitation of slow fluid flow. For mono spheres porous media sample, the relationship of permeability and porosity agrees well with the K-C equation, and the tortuosity decreases linearly with increasing porosity.


Author(s):  
Mehdi Moradkhani ◽  
Bahman Vahidi ◽  
Bahram Ahmadian

AbstractInvestigating the effects of mechanical stimuli on stem cells under in vitro and in vivo conditions is a very important issue to reach better control on cellular responses like growth, proliferation, and differentiation. In this regard, studying the effects of scaffold geometry, steady, and transient fluid flow, as well as influence of different locations of the cells lodged on the scaffold on effective mechanical stimulations of the stem cells are of the main goals of this study. For this purpose, collagen-based scaffolds and implicit surfaces of the pore architecture was used. In this study, computational fluid dynamics and fluid-structure interaction method was used for the computational simulation. The results showed that the scaffold microstructure and the pore architecture had an essential effect on accessibility of the fluid to different portions of the scaffold. This leads to the optimization of shear stress and hydrodynamic pressure in different surfaces of the scaffold for better transportation of oxygen and growth factors as well as for optimized mechanoregulative responses of cell–scaffold interactions. Furthermore, the results indicated that the HP scaffold provides more optimizer surfaces to culture stem cells rather than Gyroid and IWP scaffolds. The results of exerting oscillatory fluid flow into the HP scaffold showed that the whole surface of the HP scaffold expose to the shear stress between 0.1 and 40 mPa and hydrodynamics factors on the scaffold was uniform. The results of this study could be used as an aid for experimentalists to choose optimist fluid flow conditions and suitable situation for cell culture.


Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 319
Author(s):  
Hongyue Yang ◽  
Songling Wang ◽  
Chunxi Li ◽  
Hengfan Li

As marine biofouling seriously affects the development and utilization of oceans, the antifouling technology of microstructured surface has become a research hotspot due to its green and environmentally friendly advantages. In the present research, the motion models of microorganisms on the surfaces of five rectangular micropits, in co-current and counter-current flow direction, were established. Dynamic mesh technology was used to simulate the movements of microorganisms with different radii in the near-wall area, and the fluid kinematics and shear stress distributions in different-sized micropits were compared. Furthermore, moving microorganisms were included in the three-dimensional microstructure model to achieve the real situation of biofouling. Simulation results revealed that the vortex flow velocity in the micropits increased with the increase of the inlet flow velocity and the existence of the vortex flow effectively reduced the formation of conditioning layers in the micropits. In the downstream and countercurrent directions, the average shear stresses on the wall decreased with the increase of the micropit depth and width, and the shear stress on the inner wall of the Mp1 micropit (a patterned surface arranged with cubes of 2 µm × 2 µm × 2 µm) was found to be the largest. A low shear stress region with a low flow velocity was formed around microorganisms in the process of approaching the microstructured surface. The shear stress gradient of micro-ridge steps increased with the approach of microorganisms, indicating that microridge edges had a better effect on reducing microbial attachment.


Author(s):  
Prithiv K R Kumar

Stem cells have the capacity to differentiate into any type of cell or organ. Stems cell originate from any part of the body, including the brain. Brain cells or rather neural stem cells have the capacitive advantage of differentiating into the central nervous system leading to the formation of neurons and glial cells. Neural stem cells should have a source by editing DNA, or by mixings chemical enzymes of iPSCs. By this method, a limitless number of neuron stem cells can be obtained. Increase in supply of NSCs help in repairing glial cells which in-turn heal the central nervous system. Generally, brain injuries cause motor and sensory deficits leading to stroke. With all trials from novel therapeutic methods to enhanced rehabilitation time, the economy and quality of life is suppressed. Only PSCs have proven effective for grafting cells into NSCs. Neurons derived from stem cells is the only challenge that limits in-vitro usage in the near future.


Impact ◽  
2018 ◽  
Vol 2018 (3) ◽  
pp. 26-28
Author(s):  
Jonathan Dawson ◽  
Richard Oreffo

Gels made from clay could provide an environment able to stimulate stem-cells due to their ability to bind biological molecules. That molecules stick to clay has been known by scientists since the 1960s. Doctors observed that absorption into the blood stream of certain drugs was severely reduced when patients were also receiving clay-based antacid or anti-diarrhoeal treatments. This curious phenomenon was realized to be due to binding of the drugs by clay particles. This interaction is now routinely harnessed in the design of tablets to carefully control the release and action of a drug. Dr Dawson now proposes to use this property of clay to create micro-environments that could stimulate stem cells to regenerate damaged tissues such as bone, cartilage or skin. The rich electrostatic properties of nano (1 millionth of a millimetre) -scale clay particles which mediate these interactions could allow two hurdles facing the development of stem-cell based regenerative therapies to be overcome simultaneously. The first challenge - to deliver and hold stem cells at the right location in the body - is met by the ability of clays to self-organise into gels via the electrostatic interactions of the particles with each other. Cells mixed with a low concentration (less than 4%) of clay particles can be injected into the body and held in the right place by the gel, eliminating, in many situations, the need for surgery. Clay particles can also interact with large structural molecules (polymers) which are frequently used in the development of materials (or 'scaffolds'), designed to host stem cells. These interactions can greatly improve the strength of such structures and could be applied to preserve their stability at the site of injury until regeneration is complete. While several gels and scaffold materials have been designed to deliver and hold stem cells at the site of regeneration, the ability of clay nanoparticles to overcome a second critical hurdle facing stem-cell therapy is what makes them especially exciting. Essential to directing the activity of stem-cells is the carefully controlled provision of key biological signalling molecules. However, the open structures of conventional scaffolds or gels, while essential for the diffusion of nutrients to the cells, means their ability to hold the signalling molecules in the same location as the cells is limited. The ability of clay nano-particles to bind biological molecules presents a unique opportunity to create local environments at a site of injury or disease that can stimulate and control stem-cell driven repair. Dr Dawson's early studies investigated the ability of clay gels to stimulate the growth of new blood vessels by incorporating a key molecular signal that stimulates this process, vascular endothelial growth factor (VEGF). In a manner reminiscent of the observations made in the 60s, Dr Dawson and colleagues observed that adding a drop of clay gel to a solution containing VEGF caused, after a few hours, the disappearance of VEGF from the solution as it became bound to the gel. When placed in an experimental injury model, the gel-bound VEGF stimulated a cluster of new blood vessels to form. These exciting results indicate the potential of clay nanoparticles to create tailor-made micro-environments to foster stem cell regeneration. Dr Dawson is developing this approach as a means of first exploring the biological signals necessary to successfully control stem cell behaviour for regeneration and then, using the same approach, to provide stem cells with these signals to stimulate regeneration in the body. The project will seek to test this approach to regenerate bone lost to cancer or hip replacement failure. If successful the same technology may be applied to harness stem cells for the treatment of a whole host of different scenarios, from burn victims to those suffering with diabetes or Parkinson's.


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