fiber alignment
Recently Published Documents


TOTAL DOCUMENTS

298
(FIVE YEARS 73)

H-INDEX

32
(FIVE YEARS 5)

2021 ◽  
Vol 9 (11) ◽  
pp. e3687
Author(s):  
Ewa Komorowska-Timek ◽  
Anna Jaźwiec ◽  
Nicholas S. Adams ◽  
Matthew P. Fahrenkopf ◽  
Alan T. Davis

2021 ◽  
Vol 233 (5) ◽  
pp. e11
Author(s):  
Rakesh Gurrala ◽  
C. Ethan Byrne ◽  
Loren M. Brown ◽  
Rafael Felix P. Tiongco ◽  
Elizabeth C. Marrin ◽  
...  

2021 ◽  
Vol 22 (20) ◽  
pp. 11215
Author(s):  
Chih-Hao Chen ◽  
Dai-Ling Li ◽  
Andy Deng-Chi Chuang ◽  
Banendu Sunder Dash ◽  
Jyh-Ping Chen

To recreate the in vivo niche for tendon tissue engineering in vitro, the characteristics of tendon tissue underlines the use of biochemical and biophysical cues during tenocyte culture. Herein, we prepare core-sheath nanofibers with polycaprolactone (PCL) sheath for mechanical support and hyaluronic acid (HA)/platelet-rich plasma (PRP) core for growth factor delivery. Three types of core-sheath nanofiber membrane scaffolds (CSNMS), consisting of random HA-PCL nanofibers (Random), random HA/PRP-PCL nanofibers (Random+) or aligned HA/PRP-PCL (Align+) nanofibers, were used to study response of rabbit tenocytes to biochemical (PRP) and biophysical (fiber alignment) stimulation. The core-sheath structures as well as other pertinent properties of CSNMS have been characterized, with Align+ showing the best mechanical properties. The unidirectional growth of tenocytes, as induced by aligned fiber topography, was confirmed from cell morphology and cytoskeleton expression. The combined effects of PRP and fiber alignment in Align+ CSNMS lead to enhanced cell proliferation rates, as well as upregulated gene expression and marker protein synthesis. Another biophysical cue on tenocytes was introduced by dynamic culture of tenocyte-seeded Align+ in a bioreactor with cyclic tension stimulation. Augmented by this biophysical beacon from mechanical loading, dynamic cell culture could shorten the time for tendon maturation in vitro, with improved cell proliferation rates and tenogenic phenotype maintenance, compared to static culture. Therefore, we successfully demonstrate how combined use of biochemical/topographical cues as well as mechanical stimulation could ameliorate cellular response of tenocytes in CSNMS, which can provide a functional in vitro environmental niche for tendon tissue engineering.


2021 ◽  
pp. 102419
Author(s):  
Nava Raj Khatri ◽  
Md. Nurul Islam ◽  
Peng-Fei Cao ◽  
Rigoberto C. Advincula ◽  
Wonbong Choi ◽  
...  

2021 ◽  
Author(s):  
TAKANORI SUGIURA ◽  
AKINORI YOSHIMURA ◽  
MASAHIRO ARAI ◽  
KEITA GOTO

The paper proposes a numerical multiscale homogenization method for carbon fiber reinforced composites, where fiber alignment is disturbed due to unintended imperfections (fiber waviness). Imperfection is introduced as input to the calculation, and the calculation is always done using idealized perfect geometry. This has a distinct advantage in numerical calculations where the same mesh can be used for a series of imperfect geometries. The calculation is based on second-order perturbation method in order to capture the anisotropy which is the feature of CFRP. The proposed method is validated by comparing the results to those of a conventional calculation. The results demonstrate that the proposed method can accurately capture the stress distribution when the amplitude of the imperfection is small.


2021 ◽  
Author(s):  
Xingyu Chen ◽  
Dongning Chen ◽  
Ehsan Ban ◽  
Paul A. Janmey ◽  
Rebecca G. Wells ◽  
...  

AbstractCells can sense and respond to mechanical forces in fibrous extracellular matrices (ECM) over distances much greater than their size. This phenomenon, termed long-range force transmission, is enabled by the realignment (buckling) of collagen fibers along directions where the forces are tensile (compressive). However, whether other key structural components of the ECM, in particular glycosaminoglycans (GAGs), can affect the efficiency of cellular force transmission remains unclear. Here we developed a theoretical model of force transmission in collagen networks with interpenetrating GAGs, capturing the competition between tension-driven collagen-fiber alignment and the swelling pressure induced by GAGs. Using this model, we show that the swelling pressure provided by GAGs increases the stiffness of the collagen network by stretching the fibers in an isotropic manner. We found that the GAG-induced swelling pressure can help collagen fibers resist buckling as the cells exert contractile forces. This mechanism impedes the alignment of collagen fibers and decreases long-range cellular mechanical communication. We experimentally validated the theoretical predictions by comparing collagen fiber alignment between cellular spheroids cultured on collagen gels versus collagen-GAG co-gels. We found significantly less alignment of collagen in collagen-GAG co-gels, consistent with the prediction that GAGs can prevent collagen fiber alignment. The roles of GAGs in modulating force transmission uncovered in this work can be extended to understand pathological processes such as the formation of fibrotic scars and cancer metastasis, where cells communicate in the presence of abnormally high concentrations of GAGs.Statement of significanceGlycosaminoglycans (GAGs) are carbohydrates that are expressed ubiquitously in the human body and are among the key macromolecules that influence development, homeostasis, and pathology of native tissues. Abnormal accumulation of GAGs has been observed in metabolic disorders, solid tumors, and fibrotic tissues. Here we theoretically and experimentally show that tissue swelling caused by the highly polar nature of GAGs significantly affects the mechanical interactions between resident cells by altering the organization and alignment of the collagenous extracellular matrix. The roles of GAGs in modulating cellular force transmission revealed here can guide the design of biomaterial scaffolds in regenerative medicine and provides insights on the role of cell-cell communication in tumor progression and fibrosis.


Sign in / Sign up

Export Citation Format

Share Document