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1.
Biophys J ; 123(7): 909-919, 2024 Apr 02.
Article in English | MEDLINE | ID: mdl-38449309

ABSTRACT

Cell proliferation plays a crucial role in regulating tissue homeostasis and development. However, our understanding of how cell proliferation is controlled in densely packed tissues is limited. Here we develop a computational framework to predict the patterns of cell proliferation in growing epithelial tissues, connecting single-cell behaviors and cell-cell interactions to tissue-level growth. Our model incorporates probabilistic rules governing cell growth, division, and elimination, also taking into account their feedback with tissue mechanics. In particular, cell growth is suppressed and apoptosis is enhanced in regions of high cell density. With these rules and model parameters calibrated using experimental data for epithelial monolayers, we predict how tissue confinement influences cell size and proliferation dynamics and how single-cell physical properties influence the spatiotemporal patterns of tissue growth. In this model, mechanical feedback between tissue confinement and cell growth leads to enhanced cell proliferation at tissue boundaries, whereas cell growth in the bulk is arrested, recapitulating experimental observations in epithelial tissues. By tuning cellular elasticity and contact inhibition of proliferation we can regulate the emergent patterns of cell proliferation, ranging from uniform growth at low contact inhibition to localized growth at higher contact inhibition. We show that the cell size threshold at G1/S transition governs the homeostatic cell density and tissue turnover rate, whereas the mechanical state of the tissue governs the dynamics of tissue growth. In particular, we find that the cellular parameters affecting tissue pressure play a significant role in determining the overall growth rate. Our computational study thus underscores the impact of cell mechanical properties on the spatiotemporal patterns of cell proliferation in growing epithelial tissues.


Subject(s)
Cell Communication , Epithelial Cells , Cell Proliferation , Epithelium , Cell Cycle
2.
bioRxiv ; 2023 Jul 27.
Article in English | MEDLINE | ID: mdl-37546964

ABSTRACT

Cell proliferation plays a crucial role in regulating tissue homeostasis and development. However, our understanding of how cell proliferation is controlled in densely packed tissues is limited. Here we develop a computational framework to predict the patterns of cell proliferation in growing tissues, connecting single-cell behaviors and cell-cell interactions to tissue-level growth. Our model incorporates probabilistic rules governing cell growth, division, and elimination, while also taking into account their feedback with tissue mechanics. In particular, cell growth is suppressed and apoptosis is enhanced in regions of high cell density. With these rules and model parameters calibrated using experimental data, we predict how tissue confinement influences cell size and proliferation dynamics, and how single-cell physical properties influence the spatiotemporal patterns of tissue growth. Our findings indicate that mechanical feedback between tissue confinement and cell growth leads to enhanced cell proliferation at tissue boundaries, whereas cell growth in the bulk is arrested. By tuning cellular elasticity and contact inhibition of proliferation we can regulate the emergent patterns of cell proliferation, ranging from uniform growth at low contact inhibition to localized growth at higher contact inhibition. Furthermore, mechanical state of the tissue governs the dynamics of tissue growth, with cellular parameters affecting tissue pressure playing a significant role in determining the overall growth rate. Our computational study thus underscores the impact of cell mechanical properties on the spatiotemporal patterns of cell proliferation in growing tissues.

3.
Sports (Basel) ; 11(2)2023 Feb 09.
Article in English | MEDLINE | ID: mdl-36828329

ABSTRACT

The purpose of this study was to compare the propulsion phase characteristics of the jump squat (JS), hexagonal barbell jump (HEXJ), and jump shrug (JShrug) performed across a spectrum of relative loads. Thirteen resistance-trained women (18-23 years old) performed JS, HEXJ, and JShrug repetitions at body mass (BM) or with 20, 40, 60, 80, or 100% BM during three separate testing sessions. Propulsion mean force (MF), duration (Dur), peak power output (PP), force at PP (FPP), and velocity at PP (VPP) were compared between exercises and loads using a series of 3 × 6 repeated measures ANOVA and Hedge's g effect sizes. There were no significant differences in MF or Dur between exercises. While load-averaged HEXJ and JShrug PP were significantly greater than the JS, there were no significant differences between exercises at any individual load. The JShrug produced significantly greater FPP than the JS and HEXJ at loads ranging from BM-60% BM, but not at 80 or 100% BM. Load-averaged VPP produced during the JS and HEXJ was significantly greater than the JShrug; however, there were no significant differences between exercises at any individual load. Practically meaningful differences between exercises indicated that the JShrug produced greater magnitudes of force during shorter durations compared to the JS and HEXJ at light loads (BM-40%). The JS and HEXJ may be classified as more velocity-dominant exercises while the JShrug may be more force-dominant. Thus, it is important to consider the context in which each exercise is prescribed for resistance-trained women to provide an effective training stimulus.

4.
J Hum Kinet ; 68: 109-122, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31531137

ABSTRACT

The purpose of this study was to compare the power production characteristics of the jump squat (JS), hexagonal barbell jump (HEXJ), and jump shrug (JShrug) across a spectrum of relative loads. Fifteen resistance-trained men completed three testing sessions where they performed repetitions of either the JS, HEXJ, or JShrug at body mass (BM) or with 20, 40, 60, 80, or 100% of their BM. Relative peak power (PPRel), relative force at PP (FPP), and velocity at PP (VPP) were compared between exercises and loads. In addition, power-time curves at each load were compared between exercises. Load-averaged HEXJ and JShrug PPRel were statistically greater than the JS (both p < 0.01), while no difference existed between the HEXJ and the JShrug (p = 1.000). Load-averaged JShrug FPP was statistically greater than both the JS and the HEXJ (both p < 0.001), while no statistical difference existed between the JS and the HEXJ (p = 0.111). Load-averaged JS and HEXJ VPP were statistically greater than the JShrug (both p < 0.01). In addition, HEXJ VPP was statistically greater than the JS (p = 0.009). PPRel was maximized at 40, 40, and 20% BM for the JS, HEXJ, and JShrug, respectively. The JShrug possessed statistically different power-time characteristics compared to both the JS and the HEXJ during the countermovement and propulsion phases. The HEXJ and the JShrug appear to be superior exercises for PPRel compared to the JS. The HEXJ may be considered a more velocity-dominant exercise, while the JShrug may be a more force-dominant one.

6.
J Vis Exp ; (95)2015 Jan 30.
Article in English | MEDLINE | ID: mdl-25741745

ABSTRACT

Controllable electrode surface modification is important in a number of fields, especially those with solar fuels applications. Electropolymerization is one surface modification technique that electrodeposits a polymeric film at the surface of an electrode by utilizing an applied potential to initiate the polymerization of substrates in the Helmholtz layer. This useful technique was first established by a Murray-Meyer collaboration at the University of North Carolina at Chapel Hill in the early 1980s and utilized to study numerous physical phenomena of films containing inorganic complexes as the monomeric substrate. Here, we highlight a procedure for coating electrodes with an inorganic complex by performing reductive electropolymerization of the vinyl-containing poly-pyridyl complex onto glassy carbon and fluorine doped tin oxide coated electrodes. Recommendations on electrochemical cell configurations and troubleshooting procedures are included. Although not explicitly described here, oxidative electropolymerization of pyrrole-containing compounds follows similar procedures to vinyl-based reductive electropolymerization but are far less sensitive to oxygen and water.


Subject(s)
Carbon/chemistry , Electrochemical Techniques/methods , Fluorine/chemistry , Pyrroles/chemistry , Tin Compounds/chemistry , Vinyl Compounds/chemistry , Electrochemical Techniques/instrumentation , Electrodes , Oxidation-Reduction , Polymerization , Polymers/chemical synthesis , Polymers/chemistry , Pyrroles/chemical synthesis
7.
Transplantation ; 88(6): 762-5, 2009 Sep 27.
Article in English | MEDLINE | ID: mdl-19920774

ABSTRACT

INTRODUCTION: Human herpesvirus (HHV)-6 infection is common after organ transplantation; however, most cases are associated with a mild clinical course. Donor-derived infection is rare, and there are no reports of HHV-6 infection in more than one recipient from a common donor. METHODS: We describe two patients who developed severe, and in one case fatal, HHV-6 variant A infection after renal transplantation. RESULTS: Both patients presented with severe colitis followed by the development of liver dysfunction and cytopenia. Multiple specimens from both recipients were positive for HHV-6 polymerase chain reaction variant A. Serum and white cells from the donor were positive for HHV-6 DNA, suggesting a donor-derived infection in these patients. CONCLUSIONS: We report two cases of donor-derived HHV-6 infection from the same deceased donor, resulting in a fatal outcome in one patient. Treatment with valganciclovir was successfully instigated in one patient with a full recovery from the infection.


Subject(s)
Herpesvirus 6, Human , Kidney Transplantation/adverse effects , Roseolovirus Infections/transmission , Adult , Base Sequence , Colitis/etiology , Colitis/pathology , Colitis/virology , DNA Primers/genetics , DNA, Viral/genetics , DNA, Viral/metabolism , Fatal Outcome , Genetic Variation , Heart Transplantation , Herpesvirus 6, Human/genetics , Herpesvirus 6, Human/isolation & purification , Herpesvirus 6, Human/physiology , Humans , Male , Middle Aged , Roseolovirus Infections/pathology , Roseolovirus Infections/virology , Tissue Donors , Virus Replication
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