ArticleBiophysical journal2009
Influence of the partitioning of osmolytes by the cytoplasm on the passive response of cells to osmotic loading.
Article in Biophysical journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed.
- Computational study of biomechanical drivers of renal cystogenesis.Biomechanics and modeling in mechanobiology · 2023Article
- Superficial zone chondrocytes can get compacted under physiological loading: A multiscale finite element analysis.Acta biomaterialia · 2023Article
- The Protective Function of Directed Asymmetry in the Pericellular Matrix Enveloping Chondrocytes.Annals of biomedical engineering · 2022Article
- Liquid-liquid phase separation underpins the formation of replication factories in rotaviruses.The EMBO journal · 2021Article
- Inhibition of toll-like receptor 4 protects against inflammation-induced mechanobiological alterations to intervertebral disc cells.European cells & materials · 2021Article
- Actomyosin contractility confers mechanoprotection against TNFα-induced disruption of the intervertebral disc.Science advances · 2020Article
- Finite Element Formulation of Multiphasic Shell Elements for Cell Mechanics Analyses in FEBio.Journal of biomechanical engineering · 2018Article
- Inflammation induces irreversible biophysical changes in isolated nucleus pulposus cells.PloS one · 2014Article
- Multiphasic finite element framework for modeling hydrated mixtures with multiple neutral and charged solutes.Journal of biomechanical engineering · 2013Article
- Mechanics of Cell Growth.Mechanics research communications · 2012Article
- Finite element implementation of mechanochemical phenomena in neutral deformable porous media under finite deformation.Journal of biomechanical engineering · 2011Article
- Modeling of active transmembrane transport in a mixture theory framework.Annals of biomedical engineering · 2010Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Due to the dense organization of organelles, cytoskeletal elements, and protein complexes that make up the intracellular environment, it is likely that membrane-permeant solutes may be excluded from a fraction of the interstitial space of the cytoplasm via steric restrictions, electrostatic interactions, and other long-range intermolecular forces. This study investigates the hypothesis that the intracellular partitioning of membrane-permeant solutes manifests itself as a partial volume recovery in response to hyperosmotic loading, based on prior theoretical and biomimetic experimental studies. Osmotic loading experiments are performed on immature bovine chondrocytes using culture conditions where regulatory volume responses are shown to be insignificant. Osmotic loading with membrane-permeant glycerol (92 Da) and urea (60 Da) are observed to produce partial volume recoveries consistent with the proposed hypothesis, whereas loading with 1,2-propanediol (76 Da) produces complete volume recovery. Combining these experimental results with the previous theoretical framework produces a measure for the intracellular partition coefficient of each of these solutes. At 1000 mOsm, 1,2-propanediol is the only osmolyte to yield a partition coefficient not statistically different from unity, kappa(p)(i) = 1.00 +/- 0.02. For glycerol, the partition coefficient increases with osmolarity from kappa(p)(i) = 0.48 +/- 0.19 at 200 mOsm to kappa(p)(i) = 0.80 +/- 0.07 at 1000 mOsm; urea exhibits no such dependence, with an average value of kappa(p)(i) = 0.87 +/- 0.07 for all osmolarities from 200 to 1000 mOsm. The finding that intracellular partitioning of membrane-permeant solutes manifests itself as a partial volume recovery under osmotic loading offers a simple method for characterizing the partition coefficient. These measurements suggest that significant partitioning may occur even for small membrane-permeant osmolytes. Furthermore, a positive correlation is observed, suggesting that a solute's cytoplasmic partition coefficient increases with increasing hydrophobicity.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.