Biodegradable LC Oligomers with Cranked Branching Points Form Highly Oriented Fibrous Scaffold for Cytoskeletal Orientation
Source abstract
Abstract
Thermotropic liquid crystalline (LC) hyperbranch oligoesters (molecular weight of ca. 8 kDa) composed of rigid biodegradable segments, oligo{4-hydroxycinnamic acid (4HCA)}, plus a multifunctional biomolecule, cholic acid (CA), were prepared. Semiempirical calculations for the most stable conformation of the model compound CA derivatives with four arms of 4HCA tetramer showed that every arm can adopt an almost parallel orientation and that the CA unit can form a crankshaft architecture and function as a four-way junction of a branch point. Oligo(4HCA- co -CA)s successfully form molecularly oriented fibers with a high orientation degree by spinning viscous LC melts. Scanning electron microscopy demonstrated that mouse fibroblasts oriented uniaxially along the fiber longitudinal axis. Moreover, confocal fluorescence scanning microscopy showed that the RFP-stained cytoskeleton of these fibroblasts oriented highly.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Cellular Mechanics and Interactions · Silk-based biomaterials and applications · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, 565-0871 Japan
References (21)
Show source-provided references
1. Porter K. R. · 1964
2. Zhu X. · Nat. Mater. · 2005 · 4 · 40310.1038/nmat1365 ↗
3. Balaban N. Q. · Nat. Cell. Biol. · 2001 · 3 · 46610.1038/35074532 ↗
4. Poole K. · J. Mol. Biol. · 2005 · 349 · 38010.1016/j.jmb.2005.03.064 ↗
5. Co C. C. · J. Am. Chem. Soc. · 2005 · 127 · 159810.1021/ja044382a ↗
6. Clark P. · J. Cell. Sci. · 1992 · 103 · 28710.1242/jcs.103.1.287 ↗
7. Kaneko T. · Chem. Mater. · 2004 · 16 · 559610.1021/cm0490975 ↗
8. Collings P. J. · 199710.4324/9780203211199 ↗
9. Chandroasekhar S. · 199210.1017/CBO9780511622496 ↗
10. Somogyi A. · Macromolecules · 2005 · 38 · 406710.1021/ma0474022 ↗
11. Flory P. J. · J. Am. Chem. Soc. · 1952 · 74 · 271810.1021/ja01131a008 ↗
12. Kaneko T. · Macromol. Rapid Commun. · 2004 · 25 · 67310.1002/marc.200300143 ↗
13. Matsusaki M. · Biomaterials · 2005 · 26 · 626310.1016/j.biomaterials.2005.03.044 ↗
14. Matsusaki M. · J. Appl. Polym. Sci. · 2001 · 82 · 235710.1002/app.2085 ↗
15. Weng W. · Macromol. Rapid Commun. · 2001 · 22 · 148810.1002/1521-3927(20011201)22:18<1488::AID-MARC1488>3.0.CO;2-I ↗
16. Baker J. F. · J. Org. Chem. · 1975 · 40 · 157910.1021/jo00899a013 ↗
17. Hu X. · Steroids · 2005 · 70 · 53110.1016/j.steroids.2004.11.015 ↗
18. Kaufmann S. · Chem. Phys. Chem. · 2003 · 4 · 69910.1002/cphc.200200537 ↗
19. Mohammed J. S. · J. Langmuir · 2006 · 22 · 273810.1021/la0525473 ↗
20. Théry M. · Cell Motil. Cytoskeleton · 2006 · 63 · 34110.1002/cm.20126 ↗
21. Raghavan S. · Adv. Mater. · 2004 · 16 · 130310.1002/adma.200400594 ↗