scholarly journals Hemocyanin Modification of Chitosan Scaffolds with Calcium Phosphate Phases Increase the Osteoblast/Osteoclast Activity Ratio—A Co-Culture Study

Molecules ◽  
2020 ◽  
Vol 25 (19) ◽  
pp. 4580
Author(s):  
Benjamin Kruppke ◽  
Christiane Heinemann ◽  
Jana Farack ◽  
Simy Weil ◽  
Eliahu David Aflalo ◽  
...  

The ongoing research on biomaterials that support bone regeneration led to the quest for materials or material modifications that can actively influence the activity or balance of bone tissue cells. The bone biocompatibility of porous chitosan scaffolds was modified in the present study by the addition of calcium phosphates or hemocyanin. The first strategy comprised the incorporation of calcium phosphates into chitosan to create a biomimetic chitosan—mineral phase composite. The second strategy comprised dip-coating of chitosan scaffolds with hemocyanin extracted from crayfish hemolymph. The cytocompatibility was assessed in a mono-culture of human bone marrow stromal cells (hBMSCs) and their differentiation to osteoblasts; in a mono-culture of human monocytes (hMs) and their maturation to osteoclasts; and in a co-culture of hBMSC/osteoblasts—hM/osteoclasts. Mineral incorporation caused an increase in scaffold bioactivity, as shown by reduced calcium concentration in the cell culture medium, delayed differentiation of hBMSCs, and reduced osteoclastic maturation of hMs in mono-culture. Dip-coating with hemocyanin led to increased proliferation of hBMSCs and equivalent osteoclast maturation in mono-culture, while in co-culture, both an inhibitory effect of mineral incorporation on osteoblastogenesis and stimulatory effects of hemocyanin were observed. It was concluded that highly bioactive scaffolds (containing mineral phases) restrain osteoblast and osteoclast development, while hemocyanin coating significantly supports osteoblastogenesis. These influences on the osteoblasts/osteoclasts activity ratio may support scaffold-driven bone healing in the future.

2014 ◽  
Vol 34 (6) ◽  
pp. 859-870 ◽  
Author(s):  
Xingmei Feng ◽  
Xiaohui Lu ◽  
Dan Huang ◽  
Jing Xing ◽  
Guijuan Feng ◽  
...  

2011 ◽  
Vol 324 ◽  
pp. 8-13 ◽  
Author(s):  
Vincenzo Guarino ◽  
Antonio Gloria ◽  
Marco A. Alvarez-Perez ◽  
Maria Grazia Raucci ◽  
Valentina Cirillo ◽  
...  

In order to mimic the behaviors of natural tissue, the optimal approach for designing novel biomaterials has to be inspired to nature guidelines. One of the major challenge consists in the development of well-organized structures or scaffolds with controlled porosity in terms of pore size, pore shape and interconnection degree able to guide new tissue formation during the in vivo degradation following the scaffold implantation. Scaffolds endowed with molecular cues together to a controlled degradation profile should contribute to cell proliferation and differentiation, controlled vascularization, promoting the remodeling of neo tissue through a gradual transmission of bio-chemicals and biophysical signals as performed by the extracellular matrix (ECM). Here, different polymers and composites have been investigated to design scaffolds with peculiar micro and/or nanometric morphological features in order to satisfy all these requirements: a) bioactive scaffolds, with tailored porosity and high pores interconnectivity were developed by integrating PLA fibres, Calcium Phosphates particles or Hyaff11 phases into a Poly(ε-caprolactone) (PCL) matrix by the combination of filament winding technology and phase inversion/salt leaching technique as mineralised ECM analogue for bone regeneration; b) custom made PCL/hydroxyapatite scaffolds were designed by imaging and rapid prototyping technologies for the osteochondral defect. c) Ester of Hyaluronic Acid reinforced with degradable fibres were processed by composite technology, phase inversion and salt leaching technique, to obtain scaffolds for meniscus regeneration. d) PCL and gelatin nanofibres were obtained by highly customized fibre deposition via electrospinning to guide the nerve outgrowth in nerve regeneration. All the proposed approaches offer the chance of realizing tailor-made platforms with micro/nanoscale architecture and chemical composition suitable for the regeneration of the extracellular matrix of a large variety of natural tissues (i.e, bone, menisci, osteochondral and peripheral nervous tissues).


2011 ◽  
Vol 17 (21-22) ◽  
pp. 2763-2772 ◽  
Author(s):  
Jangho Kim ◽  
Seung Won Kim ◽  
Seong Jun Choi ◽  
Ki Taek Lim ◽  
Jong Bin Lee ◽  
...  

2011 ◽  
Vol 7 (4) ◽  
pp. 1653-1664 ◽  
Author(s):  
Chengdong Ji ◽  
Nasim Annabi ◽  
Ali Khademhosseini ◽  
Fariba Dehghani

2014 ◽  
Vol 91 ◽  
pp. 13-18 ◽  
Author(s):  
A. Prichodko ◽  
V. Jonauske ◽  
M. Cepenko ◽  
A. Beganskiene ◽  
A. Kareiva

Calcium hydroxyapatite (Ca10(PO4)6(OH)2, CHAp), tricalcium phosphate (Ca3(PO4)2, TCP) and calcium oxide (CaO) are the main components of inorganic part of human bones. Such synthetic nanocomposites could be very important implantable materials and using as substitute material for human hard tissues (bones and teeth). In this study, an aqueous sol-gel chemistry route has been developed to prepare nanostructured CHAp thin films on stainless steel substrate. For the preparation of thin films dip-coating and spin-coating techniques were used. The final samples were obtained by calcination of coatings for different time at 1000 °C. For the characterization of surface properties, the X-ray powder diffraction (XRD) analysis, scanning electron microscopy (SEM), atomic force microscopy (AFM) and the contact angle measurements were recorded.


2017 ◽  
Vol 8 ◽  
pp. 204173141769754 ◽  
Author(s):  
Maria Sancho-Tello ◽  
Sara Martorell ◽  
Manuel Mata Roig ◽  
Lara Milián ◽  
MA Gámiz-González ◽  
...  

The clinical management of large-size cartilage lesions is difficult due to the limited regenerative ability of the cartilage. Different biomaterials have been used to develop tissue engineering substitutes for cartilage repair, including chitosan alone or in combination with growth factors to improve its chondrogenic properties. The main objective of this investigation was to evaluate the benefits of combining activated platelet-rich plasma with a stabilized porous chitosan scaffold for cartilage regeneration. To achieve this purpose, stabilized porous chitosan scaffolds were prepared using freeze gelation and combined with activated platelet-rich plasma. Human primary articular chondrocytes were isolated and cultured in stabilized porous chitosan scaffolds with and without combination to activated platelet-rich plasma. Scanning electron microscopy was used for the morphological characterization of the resulting scaffolds. Cell counts were performed in hematoxylin and eosin–stained sections, and type I and II collagen expression was evaluated using immunohistochemistry. Significant increase in cell number in activated platelet-rich plasma/stabilized porous chitosan was found compared with stabilized porous chitosan scaffolds. Chondrocytes grown on stabilized porous chitosan expressed high levels of type I collagen but type II was not detectable, whereas cells grown on activated platelet rich plasma/stabilized porous chitosan scaffolds expressed high levels of type II collagen and type I was almost undetectable. In summary, activated platelet-rich plasma increases nesting and induces the differentiation of chondrocytes cultured on stabilized porous chitosan scaffolds.


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