Faculty Opinions recommendation of Compressive nonlinearity in the hair bundle's active response to mechanical stimulation.

2002 ◽  
Author(s):  
Peter Gillespie
Keyword(s):  
Mechanical Stimulation ◽  
Active Response

Modeling the Active Response of Cells to Mechanical Stimulation

2008 ◽  
Author(s):  
Patrick McGarry ◽  
Robert M. McMeeking ◽  
Anthony G. Evans ◽  
Vikram S. Deshpande
Keyword(s):  
Mechanical Properties ◽  
Mechanical Stimulation ◽  
Crucial Role ◽  
Extra Cellular Matrix ◽  
Active Response ◽  
Cellular Behavior ◽  
High Substrate ◽  
Surrounding Environment ◽  
Substrate Rigidity ◽  
Motile Cells

The mechanical properties of a cells surrounding environment, or extra cellular matrix (ECM), play a crucial role in cellular behavior. For example, it has been shown that cells tend to spread more on rigid substrates [1, 2] and that motile cells move from regions of low substrate rigidity to regions of high substrate rigidity [3].

Mechanical stimulation of human BON cells: Gαq involvement in 5-HT release

2001 ◽  
Vol 120 (5) ◽  
pp. A83-A83
Author(s):  
M KIM ◽  
N JAVED ◽  
F CHRISTOFI ◽  
H COOKE
Keyword(s):  
Mechanical Stimulation ◽  
Bon Cells ◽  
Stimulation Of

The effect of low magnitude mechanical stimulation (LMMS) on bone density in patients with Rett syndrome: A pilot and feasibility study

2014 ◽  
Vol 7 (2) ◽  
pp. 167-178 ◽  
Author(s):  
Sarah Y. Afzal ◽  
Anna R. Wender ◽  
Mary D. Jones ◽  
Ellen B. Fung ◽  
Elaine L. Pico
Keyword(s):  
Bone Density ◽  
Rett Syndrome ◽  
Feasibility Study ◽  
Mechanical Stimulation ◽  
Low Magnitude

Use of Flexible Materials with a Novel Pressure Driven Equibiaxial Cell Stretching Device for Mechanical Stimulation of Single Mammalian Cells

2003 ◽  
Vol 773 ◽  
Author(s):  
James D. Kubicek ◽  
Stephanie Brelsford ◽  
Philip R. LeDuc
Keyword(s):  
Cell Fate ◽  
Mechanical Stimulation ◽  
Mammalian Cells ◽  
Cellular Response ◽  
Single Cells ◽  
Complex Nature ◽  
Cellular Behavior ◽  
Cell Stretching ◽  
Stimulation Of ◽  
Pressure Driven

AbstractMechanical stimulation of single cells has been shown to affect cellular behavior from the molecular scale to ultimate cell fate including apoptosis and proliferation. In this, the ability to control the spatiotemporal application of force on cells through their extracellular matrix connections is critical to understand the cellular response of mechanotransduction. Here, we develop and utilize a novel pressure-driven equibiaxial cell stretching device (PECS) combined with an elastomeric material to control specifically the mechanical stimulation on single cells. Cells were cultured on silicone membranes coated with molecular matrices and then a uniform pressure was introduced to the opposite surface of the membrane to stretch single cells equibiaxially. This allowed us to apply mechanical deformation to investigate the complex nature of cell shape and structure. These results will enhance our knowledge of cellular and molecular function as well as provide insights into fields including biomechanics, tissue engineering, and drug discovery.

USING CRYOPRESERVED SPERM FOR CREATING STERLET BROOD STOCK

2017 ◽  
pp. 118-127
Author(s):  
Elena Nikolaevna Ponomareva ◽  
Maria Mikhailovna Belaya ◽  
Alexandra Andrianovna Krasilnikova ◽  
Alexander Nickolaevich Nevalennyy
Keyword(s):  
Liquid Nitrogen ◽  
Control Group ◽  
Test Results ◽  
Brood Stock ◽  
Active Response ◽  
Acipenser Ruthenus ◽  
Rostov Region ◽  
The Central Nervous System ◽  
Cryopreserved Sperm ◽  
Sturgeon Fish

The research on the sterlet roe artificial insemination using cryopreserved sperm was carried out in the research base of the RAS Southern Scientific Centre (the Rostov region). Reproductive cells (including cryopreserved cells), larvae, sterlet fry ( Acipenser ruthenus Linnaeus, 1758) were taken as an object of research. A half of the roe (1.7 kg) taken from female starlet was inseminated by native sperm (control group); another half was inseminated by defrosted sperm of two males, which was stored in liquid nitrogen at -196ºC during 3 years (pilot group). Incubation lasted 5 days at water temperature 14.5-18.2ºC, with daily fluctuations of temperature 1.9ºC. Roe insemination in the control group made 90%, in the pilot group - 70%. Roe embryonic growth in the control group was faster, but embryogenesis duration in the pilot group met the standard time limits. Hatching prolarvae in the control group started one hour earlier, than in the pilot group; it made 75% and 60% of all incubated roe, correspondingly. Waste during the period of larvae maturing before they pass to mixed feeding was negligible - 2% in the control group and 3.4% in the pilot group. According to the test results, "open field" of reactivity of the central nervous system in the pilot group fry didn’t change from the control group fry, but more active response to stimuli was noted in the pilot group, which is very important for fry adaptation to the conditions in natural water basins. It was established that sterlet offspring obtained with use of defrosted sexual cells does not differ from the offspring obtained using native sperm and has higher morphometric characteristics. The test results prove the possibility and practicability of using sexual cells stored in liquid nitrogen for artificial restoration and formation of sturgeon fish broodstocks.

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