A Novel Method for Polyacrylamide Gel Preparation Using N-hydroxysuccinimide-acrylamide Ester to Study Cell-Extracellular Matrix Mechanical Interactions
Source abstract
Abstract
Mechanical stimulation by the extracellular matrix (ECM) controls physiological and pathological cellular responses, such as stem cell differentiation, organogenesis, and tumor progression. Polyacrylamide (PA) gels have been widely used to study cell-ECM mechanical interactions. Typically, sulfosuccinimidyl 6-(4′-azido-2′-nitrophenylamino)hexanoate (sulfo-SANPAH) is used as a protein crosslinker in these gels. However, its low solubility, unstable binding with proteins, and high cost are barriers to its application. The objective of this study was to improve and simplify the preparation of PA gels using an economical crosslinker, N-hydroxysuccinimide-acrylamide (NHS-AA) ester, to enable increased stability in protein coating. By exposing excess NHS to the gel surface, we found an optimal ratio of NHS-AA ester:AA to obtain NHS-AA ester-containing PA gels with a uniform ECM protein coating and stiffness similar to that of sulfo-SANPAH-containing PA gels. The biological behavior of MCF7 and MCF10A cells were similar on NHS-AA ester and sulfo-SANPAH gels. Acini formation in Matrigel overlay culture were also consistent on NHS-AA ester and sulfo-SANPAH gels. This novel PA gel preparation method using NHS-AA ester can effectively replace the sulfo-SANPAH method and will be immensely useful in the evaluation of cell-ECM mechanical interactions.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Cellular Mechanics and Interactions · Tissue Engineering and Regenerative Medicine · 3D Printing in Biomedical Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (36)
Show source-provided references
1. Polysaccharide-modified synthetic polymeric biomaterials10.1002/bip.21334 ↗
2. Quantifying ligand-cell interactions and determination of the surface concentrations of ligands on hydrogel films: the measurement challenge10.1116/1.4919015 ↗
3. Fc-receptor-mediated phagocytosis is regulated by mechanical properties of the target10.1242/jcs.115.4.849 ↗
4. A tense situation: forcing tumour progression10.1038/nrc2544 ↗
5. Extracellular matrix stiffness and composition jointly regulate the induction of malignant phenotypes in mammary epithelium10.1038/nmat4009 ↗
6. Studying the effects of matrix stiffness on cellular function using acrylamide-based hydrogels10.3791/2089 ↗
7. Morphogenesis and oncogenesis of MCF-10A mammary epithelial acini grown in three-dimensional basement membrane cultures10.1016/S1046-2023(03)00032-X ↗
8. Tuning the range of polyacrylamide gel stiffness for mechanobiology applications10.1021/acsami.5b09344 ↗
9. Cellular morphology-mediated proliferation and drug sensitivity of breast cancer cells10.3390/jfb8020018 ↗
10. Role of YAP/TAZ in mechanotransduction10.1038/nature10137 ↗
11. Matrix elasticity directs stem cell lineage specification10.1016/j.cell.2006.06.044 ↗
12. Greenberg · 2000
13. Polyacrylamide hydrogels for cell mechanics: steps toward optimization and alternative uses10.1016/S0091-679X(07)83002-0 ↗
14. Basement membrane complexes with biological activity10.1021/bi00350a005 ↗
15. Effect of substrate stiffness on early mouse embryo development10.1371/journal.pone.0041717 ↗
16. Self-assembling peptide nanofiber hydrogels in tissue engineering and regenerative medicine: progress, design guidelines, and applications10.1002/jbm.a.35638 ↗
17. Facile conjugation of biomolecules onto surfaces via mussel adhesive protein inspired coatings10.1002/adma.200801222 ↗
18. Soft biological materials and their impact on cell function10.1039/b610522j ↗
19. Matrix crosslinking forces tumor progression by enhancing integrin signaling10.1016/j.cell.2009.10.027 ↗
20. Graphene improves the biocompatibility of polyacrylamide hydrogels: 3D polymeric scaffolds for neuronal growth10.1038/s41598-017-11359-x ↗
21. Identification of a mechanogenetic link between substrate stiffness and chemotherapeutic response in breast cancer10.1016/j.biomaterials.2019.02.018 ↗
22. Modulating alginate hydrogels for improved biological performance as cellular 3D microenvironments10.3389/fbioe.2020.00665 ↗
23. Collagen-Based biomaterials for tissue engineering applications10.3390/ma3031863 ↗
24. The tension mounts: mechanics meets morphogenesis and malignancy10.1007/s10911-004-1404-x ↗
25. Tensional homeostasis and the malignant phenotype10.1016/j.ccr.2005.08.010 ↗
26. Cell locomotion and focal adhesions are regulated by substrate flexibility10.1073/pnas.94.25.13661 ↗
27. Polyacrylamide gels copolymerized with active esters. A new medium for affinity systems10.1021/bi00678a030 ↗
28. Adhesion of chicken hepatocytes to polyacrylamide gels derivatized with N-acetylglucosamine10.1016/S0021-9258(17)34462-9 ↗
29. Matrix rigidity regulates cancer cell growth and cellular phenotype10.1371/journal.pone.0012905 ↗
30. Preparation of hydrogel substrates with tunable mechanical properties10.1002/0471143030.cb1016s47 ↗
31. Hydrogel as a bioactive material to regulate stem cell fate10.1016/j.bioactmat.2016.05.001 ↗
32. Interplay of matrix stiffness and protein tethering in stem cell differentiation10.1038/NMAT4051 ↗
33. Dynamic heterodimer-functionalized surfaces for endothelial cell adhesion10.1016/j.biomaterials.2004.11.060 ↗
34. Development of three-dimensional cell culture scaffolds using laminin peptide-conjugated agarose microgels10.1021/acs.biomac.0c00871 ↗
35. Cellular response to substrate rigidity is governed by either stress or strain10.1016/j.bpj.2012.11.3805 ↗
36. Bioactive modification of poly(ethylene glycol) hydrogels for tissue engineering10.1016/j.biomaterials.2010.02.044 ↗