Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Cell-matrix's Response to Mechanical Forces01:13

Cell-matrix's Response to Mechanical Forces

3.3K
In animal cells, the extracellular matrix allows cells within tissues to withstand external stresses and transmits signals from the outside of the cell to the inside. The extracellular matrix is extensive, and its composition varies between different types of tissues. For example, the reticular fibers and ground substance make up the ECM in loose connective tissue, while collagen and bone minerals make up the ECM of bone tissue. 
Anchoring junctions mechanically attach a cell to the...
3.3K
Cell Adhesion in Plants01:14

Cell Adhesion in Plants

3.1K
Plants have rigid cell walls that are made up of cell wall polysaccharides that mediate cell-cell adhesion. The primary cell walls of plants consist of two independent and interacting polysaccharide networks: a pectin matrix that embeds the second network comprising cellulose and hemicelluloses.
Pectins are complex heteropolymers mainly composed of negatively-charged α-D-glucopyranosyl uronic acid and some neutral glycosyl residues such as α-L-rhamnopyranose, α-L-arabinofuranose,...
3.1K
Role of Microtubules in Cell Wall Deposition01:02

Role of Microtubules in Cell Wall Deposition

2.8K
Microtubules are small hollow tubes in eukaryotic cells. The cell wall microtubules are polymerized dimers of two globular proteins, α-tubulin and β-tubulin, two globular proteins. With a diameter of about 25 nm, microtubules are the widest components of the cytoskeleton. They help the cell resist compression and provide a track along which vesicles move through the cell or pull replicated chromosomes to opposite ends of a dividing cell. Microtubules go through quick cycles of...
2.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Glucose-6-phosphate dehydrogenase variants modify 3D genomic organization to suppress maladaptive gene expression and vascular disease.

The Journal of biological chemistry·2026
Same author

Engineering a Matrix-Preserving Vascular dECM Platform with Tunable Stiffness for <i>In Vitro</i> Vascular Remodeling.

bioRxiv : the preprint server for biology·2026
Same author

ARHGAP18 complexes with both YAP and Merlin and is required for basal actin bundles.

Molecular biology of the cell·2026
Same author

Closing the Loop on E-waste: A Multidisciplinary Perspective.

Journal of industrial ecology·2026
Same author

Mechanotherapeutic Potential of Survivin in Glioblastoma.

bioRxiv : the preprint server for biology·2026
Same author

Low-Density InGaAs/AlGaAs Quantum Dots in Droplet-Etched Nanoholes.

Nano letters·2026

Related Experiment Video

Updated: Dec 30, 2025

Preparation of Tunable Extracellular Matrix Microenvironments to Evaluate Schwann Cell Phenotype Specification
07:50

Preparation of Tunable Extracellular Matrix Microenvironments to Evaluate Schwann Cell Phenotype Specification

Published on: June 2, 2020

5.7K

Modulating cell response on cellulose surfaces; tunable attachment and scaffold mechanics.

James C Courtenay1,2, Christoph Deneke3, Evandro M Lanzoni3

  • 11Centre for Sustainable Chemical Technologies, University of Bath, Bath, BA2 7AY UK.

Cellulose (London, England)
|January 28, 2020
PubMed
Summary

Surface modification of cellulose with positively charged groups enhances mammalian cell attachment. Tuning scaffold stiffness further regulates cell morphology, offering new biomaterial possibilities without protein additives.

Keywords:
Cell responseCelluloseChemical modificationSimple manufactureTunable tissue scaffold

More Related Videos

Simple Polyacrylamide-based Multiwell Stiffness Assay for the Study of Stiffness-dependent Cell Responses
07:45

Simple Polyacrylamide-based Multiwell Stiffness Assay for the Study of Stiffness-dependent Cell Responses

Published on: March 25, 2015

20.5K
Generation of Multicue Cellular Microenvironments by UV-Photopatterning of Three-Dimensional Cell Culture Substrates
09:30

Generation of Multicue Cellular Microenvironments by UV-Photopatterning of Three-Dimensional Cell Culture Substrates

Published on: June 2, 2022

2.8K

Related Experiment Videos

Last Updated: Dec 30, 2025

Preparation of Tunable Extracellular Matrix Microenvironments to Evaluate Schwann Cell Phenotype Specification
07:50

Preparation of Tunable Extracellular Matrix Microenvironments to Evaluate Schwann Cell Phenotype Specification

Published on: June 2, 2020

5.7K
Simple Polyacrylamide-based Multiwell Stiffness Assay for the Study of Stiffness-dependent Cell Responses
07:45

Simple Polyacrylamide-based Multiwell Stiffness Assay for the Study of Stiffness-dependent Cell Responses

Published on: March 25, 2015

20.5K
Generation of Multicue Cellular Microenvironments by UV-Photopatterning of Three-Dimensional Cell Culture Substrates
09:30

Generation of Multicue Cellular Microenvironments by UV-Photopatterning of Three-Dimensional Cell Culture Substrates

Published on: June 2, 2022

2.8K

Area of Science:

  • Biomaterials Science
  • Surface Chemistry
  • Cell Biology

Background:

  • Cell attachment and morphology are crucial for biomaterial performance.
  • Current methods often rely on protein modifiers or ligands for cell adhesion.
  • Developing cell-instructive biomaterials without exogenous agents is a significant challenge.

Purpose of the Study:

  • To chemically modify cellulose surfaces to promote direct mammalian cell attachment.
  • To investigate the influence of surface charge and scaffold stiffness on cell behavior.
  • To create novel functionalized cellulose biomaterials for cell support and morphology regulation.

Main Methods:

  • Cellulose surface modification via reaction with glycidyltrimethylammonium chloride (GTMAC) to introduce trimethylammonium groups.
  • Quantification of surface charge using ζ-potential and electric force microscopy.
  • Modulation of cellulose film stiffness through glyoxal crosslinking and measurement via atomic force microscopy.
  • Assessment of MG-63 cell attachment and morphology on modified cellulose scaffolds.

Main Results:

  • A low degree of substitution (1.4%) of cationic groups on cellulose significantly increased MG-63 cell attachment (>90%).
  • Cell attachment plateaued at higher degrees of substitution (ca. 1.85%), correlating with surface charge.
  • Cell morphology could be effectively regulated by tuning scaffold stiffness (76-448 kPa) via crosslinking.
  • Direct cell attachment and morphology control were achieved without protein modifiers.

Conclusions:

  • Tailored cationic cellulose biomaterials can be synthesized through surface functionalization and crosslinking.
  • These materials promote direct mammalian cell attachment and allow for tunable control over cell morphology.
  • This approach represents a significant advancement towards cell-instructive biomaterials for implantation, utilizing only scaffold and cell interactions.