The use of the mechanical microenvironment of phospholipid polymer hydrogels to control cell behavior

Biomaterials ◽  
2013 ◽  
Vol 34 (24) ◽  
pp. 5891-5896 ◽  
Author(s):  
Haruka Oda ◽  
Tomohiro Konno ◽  
Kazuhiko Ishihara
2018 ◽  
Vol 130 (32) ◽  
pp. 10383-10387 ◽  
Author(s):  
Hao Li ◽  
Miao Wang ◽  
Tianhui Shi ◽  
Sihui Yang ◽  
Jinghui Zhang ◽  
...  

2004 ◽  
Vol 43 (6B) ◽  
pp. 3806-3809 ◽  
Author(s):  
Wen-Ta Su ◽  
Jung-Yen Yang ◽  
Chuan-Ding Lin ◽  
I-Ming Chu
Keyword(s):  

2019 ◽  
Vol 81 (1) ◽  
pp. 585-605 ◽  
Author(s):  
Haguy Wolfenson ◽  
Bo Yang ◽  
Michael P. Sheetz

It is increasingly clear that mechanotransduction pathways play important roles in regulating fundamental cellular functions. Of the basic mechanical functions, the determination of cellular morphology is critical. Cells typically use many mechanosensitive steps and different cell states to achieve a polarized shape through repeated testing of the microenvironment. Indeed, morphology is determined by the microenvironment through periodic activation of motility, mechanotesting, and mechanoresponse functions by hormones, internal clocks, and receptor tyrosine kinases. Patterned substrates and controlled environments with defined rigidities limit the range of cell behavior and influence cell state decisions and are thus very useful for studying these steps. The recently defined rigidity sensing process provides a good example of how cells repeatedly test their microenvironment and is also linked to cancer. In general, aberrant extracellular matrix mechanosensing is associated with numerous conditions, including cardiovascular disease, aging, and fibrosis, that correlate with changes in tissue morphology and matrix composition. Hence, detailed descriptions of the steps involved in sensing and responding to the microenvironment are needed to better understand both the mechanisms of tissue homeostasis and the pathomechanisms of human disease.


2018 ◽  
Vol 57 (32) ◽  
pp. 10226-10230 ◽  
Author(s):  
Hao Li ◽  
Miao Wang ◽  
Tianhui Shi ◽  
Sihui Yang ◽  
Jinghui Zhang ◽  
...  

2017 ◽  
Vol 216 (12) ◽  
pp. 3889-3890
Author(s):  
Marie Anne O’Donnell
Keyword(s):  

Rusan investigates how centrosomes control cell behavior and differentiation during development.


2007 ◽  
Vol 342-343 ◽  
pp. 777-780 ◽  
Author(s):  
Mizuna Kimura ◽  
Tomohiro Konno ◽  
Madoka Takai ◽  
Noriyuki Ishiyama ◽  
Toru Moro ◽  
...  

We investigated phospholipid polymer hydrogels containing Fe3+ ions (PMA/PMB/Fe hydrogel) for their use as antiadhesive materials in the healing tissues. These hydrogels were prepared from the aqueous solutions of poly(2-methacryloyloxyethyl phosphorylcholine (MPC)-comethacrylic acid) (PMA) and poly(MPC-co-n-butyl methacrylate) (PMB). The PMA/PMB hydrogel is formed by the intermolecular interactions between PMA and PMB, and it reversibly dissociates under physiological conditions. The addition of Fe3+ ions could control the gelation time and the dissociation time. Mechanical properties such as the gelation time and viscoelastic properties can be controlled by the FeCl3 concentration. With regard to biocompatibility, no evidence of inflammation was observed in vivo. Therefore, the PMA/PMB/Fe hydrogel has a potential to be used as an antiadhesive material.


2012 ◽  
Vol 197 (3) ◽  
pp. 351-360 ◽  
Author(s):  
Deok-Ho Kim ◽  
Paolo P. Provenzano ◽  
Chris L. Smith ◽  
Andre Levchenko

The architecture of the extracellular matrix (ECM) directs cell behavior by providing spatial and mechanical cues to which cells respond. In addition to soluble chemical factors, physical interactions between the cell and ECM regulate primary cell processes, including differentiation, migration, and proliferation. Advances in microtechnology and, more recently, nanotechnology provide a powerful means to study the influence of the ECM on cell behavior. By recapitulating local architectures that cells encounter in vivo, we can elucidate and dissect the fundamental signal transduction pathways that control cell behavior in critical developmental, physiological, and pathological processes.


Author(s):  
Laxminarayanan Krishnan ◽  
Carlos C. Chang ◽  
Shawn Reese ◽  
Stuart K. Williams ◽  
Jeffrey A. Weiss ◽  
...  

One of the challenges in engineering complex artificial tissue constructs, with defined matrix and cellular architecture, is the formation of a viable microcirculation within them, that inosculates with the host vasculature and matures into a functional microvascular bed. Current methods based on complex cell patterning in 2-D or 3-D matrix systems rely on ‘printing’ cells or patterns of cells on/ in a substrate, direct culture on patterned substrates, or endothelialization of decellularized vessels. We are now beginning to understand the effects of the microenvironment on microvascular constructs. Flow induced remodeling and maturation of angiogenic microvasculature and changes in functional characteristics when co-implanted with astrocyte precursors strongly suggests a role for the local environment in determining characteristics of the microvascular bed [1, 2]. Chang et al. have shown that neovascular networks from microvessels pre-aligned by direct-bioprinting in a collagen matrix, retain alignment when cultured in vitro, but lose alignment on implantation in vivo [3]. Though unloading of mechanically loaded tissue influences cell behavior [4], it does not explain this loss of orientation after implantation, of previously unloaded constructs. Implanted constructs have an additional level of complexity in the form of network revision and maturation with blood flow. We hypothesize that the local mechanical microenvironment, in addition to flow, dictates network morphology in vivo. This study compares the changes in pre-aligned microvascular networks implanted with and without anchorage.


Sign in / Sign up

Export Citation Format

Share Document