grant

Mechanics of cell growth and division

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 1 Jul 2021Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY2025AgingBiological FunctionBiological ProcessCancersCell BodyCell CycleCell Division CycleCell FunctionCell NucleusCell PhysiologyCell ProcessCell WallCell divisionCellsCellular AssayCellular ExpansionCellular FunctionCellular GrowthCellular MatrixCellular PhysiologyCellular ProcessCellular biologyChromosomesCollectionCrowdingCytoplasmCytoskeletal SystemCytoskeletonDNA Damage RepairDNA RepairDevelopmentDiseaseDisorderEnvironmentFission YeastFoundationsGoalsHydrogen OxideImageInvestigationLifeM PhaseMalignant NeoplasmsMalignant TumorMechanicsMicro-tubuleMicrotubulesMitosisMitosis StageMitotic spindleMolecularMolecular Dynamics SimulationMotilityNuclearNucleic AcidsNucleoplasmNucleusOrganellesOsmotic PressurePathogenesisPhasePhysiologicPhysiologicalProcessProteinsRheologyS pombeS. pombeSchizosaccharomyces pombeSubcellular ProcessUnscheduled DNA SynthesisWaterWorkbiophysical characteristicsbiophysical characterizationbiophysical measurementbiophysical parametersbiophysical propertiescell assaycell biologycell growthdensitydevelopmentalimaginginnovateinnovationinnovativeintracellular skeletonmacromoleculemalignancymechanicmechanicalmolecular dynamicsneoplasm/cancersmall molecule
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Full Description

Project Summary/ Abstract
The cytoplasm is a crowded subcellular environment that is packed with organelles, proteins, nucleic acids

and other large macromolecules, as well as water and small molecules. How cell biological processes

function in this milieu remains poorly understood. Macromolecules present in the cytoplasm are thought to

exert physical forces that contribute to cytoplasmic organization, phase separation, and osmotic pressure.

Cellular density, which is the concentration of cellular components such as proteins and nucleic acids, is a

key predictor of these macromolecular crowding effects. Recent evidence from our lab and others reveals

that density and macromolecular crowding effects are not constant but actually change during the cell cycle,

as well in various physiological and disease states, and during development. However, little is known about

how these changes impact cellular physiology and mechanics. Thus, cellular density and the effects of

macromolecular crowding represent critical but understudied aspects of cellular physiology that likely impact

most cellular processes.

The general goals are to elucidate physical- and molecular- based mechanisms responsible for

cellular processes responsible for cell growth and division: mitosis, microtubule dynamics, nuclear size

control, chromosome mobility and cell wall assembly. A general thrust of the investigations is to determine

how the biophysical properties of the cytoplasm and nucleoplasm impact these diverse cellular processes.

In particular, our studies will address how intracellular osmotic pressures generated by macromolecules act

to dampen microtubule dynamics, inflate the nucleus, modulate the mechanics of the mitotic spindle, and

regulate chromosome motility for DNA repair. Approaches include innovative live cell assays for the

biophysical properties of living cells (e.g. microrheology and quantitative phase imaging) and quantitative

cell biology approaches in the fission yeast Schizosaccharomyces pombe.

These studies will establish a foundation for the emerging field of cellular density and will contribute

to our understanding of a fundamental but understudied aspect of cell biology. This work will significantly

impact our understanding of mechanisms governing cell growth and division that are relevant for biomedical

applications including cancer, aging and fungal pathogenesis.

Grant Number: 5R35GM141796-05
NIH Institute/Center: NIH

Principal Investigator: Fred Chang

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