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Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Tianjin Medical Journal is the property of Tianjin Medical Journal and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Functional Polymers is the property of Journal of Functional Polymers and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Graphene derivatives are the new bioactive material with good physical and chemical properties and excellent biocompatibility. It has been found that graphene derivatives can improve the mechanical properties of biomaterials and promote the adhesion, proliferation and differentiation of osteoblast-related cells, so as to promote implant-bone bonding and repair of bone defects. This makes it a research hotpot in the field of bone tissue regeneration. In this paper, the mechanism of graphene derivatives promoting bone regeneration and their application in the oral field were reviewed, so as to provide theoretical basis for their application in basic and clinical research.

BACKGROUND: Since non-coding RNAs maintain bone homeostasis through various pathways, applications of non-coding RNAs as bioactive molecules in bone tissue engineering for bone defect repair has become an increasing area of interest. OBJECTIVE: To introduce non-coding RNAs as bioactive molecules in bone tissue engineering. METHODS: A computer-based online search of Web of Science, PubMed, SpringerLink databases was performed by the first author between December 2018 and March 2019 using the search terms "bone tissue engineering, ncRNA (miRNA, siRNA or lncRNA), scaffold, drug delivery system" to retrieve papers published during 2004-2019. A total of 1754 papers were preliminarily retrieved, and 95 of them were eligible for final analysis. RESULTS AND CONCLUSION: Because non-coding RNAs play a key role in osteogenic differentiation, they can be used as important bioactive factors for bone tissue engineering. At present, bone tissue engineering repair methods based on non-coding RNA bioactive factors have become a research hotspot in bone defect repair. There are two major application strategies: (1) The non-coding RNA transcription within the seed cells is purposefully altered and combines with the bone tissue-engineered scaffold to promote bone defect repair. (2) a specifically designed bone engineered scaffold can controllably and purposefully alter the expression of non-coding RNA in the seed cells, which promotes bone defect repair. In addition, the function of more and more non-coding RNAs has been identified in the process of bone regeneration. This shows good application prospects of non-coding RNAs. [ABSTRACT FROM AUTHOR]

This paper reviewed the research status of the microstructure of scaffold pores from five aspects, including the pore shape, pore size, porosity, surface roughness, and connection pathways of bone tissue engineering scaffolds. The pore shape of the scaffold with a gradient structure was found to be closer to those of the natural bone. The rough surface can improve the cell adhesion and proliferation of the scaffolds, and the internal structure of the non-orthogonal connection pathway can provide a dynamic growth space for later bone regeneration. [ABSTRACT FROM AUTHOR]

Purpose: The aim of this meta analysis was to assess the influence of platelet-rich plasma (PRP)combined with demineralized freeze-dried bone allografts(DFDBA) on regeneration of periodontal periodontal defects by means of evaluating clinical and radiographic outcomes in prospective human clinical trials., Methods: The following databases such as PubMed, The Cochrane Library, EMbase, CNKI, Wanfang data and VIP data were searched on computer from inception to December, 2016. According to the inclusion and exclusion criteria, two reviewers independently extracted the data，assessed the methodological quality of the included studies. RevMan 5.2 was applied for meta analysis., Results: Six papers were obtained reviewed which included 205 periodontal bone defect sites. Six articles showed that there was no significant difference in probing depth decrease between PRP combined with DFDBA and PRP or DFBDA group[MD=0.35, 95%CI（-0.09，0.79), P=0.12], but there was significant difference in clinical attachment loss increase between the two groups［MD= 0.68，95%CI（0.41，0.94），P<0.00001]. Three articles were included for evaluating bone filling, there was significant difference in the distance from the cemento-enamel junction(CEJ) to the vertical bone defect(BD)(CEJ-BD)[MD=0.71，95%CI（0.46，0.95），P<0.00001]between the two groups; there was also significant difference in the distance from the alveolar crest to the vertical bone defect(AC-BD)[MD=0.64，95%CI（0.41，0.87)，P<0.00001]between the two groups. but there was no significant difference in the distance from the cemento-enamel junction(CEJ)to the alveolar crest (AC)(CEJ-AC)[MD=0.03，95%CI（-0.10，0.16），P=0.68] between the two groups., Conclusions: Within the limitations of this meta analysis, PRP combined with DFDBA is superior to PRP or DFDBA alone in clinical attachment loss and bone filling ,but there was no significant difference in probing depth. However, given the limited sample size and quantity of included studies, the above findings still need to be further proved by conducting more high-quality and large-scale RCTs.

Copyright of Journal of Prevention & Treatment For Stomatological Diseases is the property of Journal of Prevention & Treatment For Stomatological Diseases Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Tissue engineered bone ( TEB), due to its wide range of materials, excellent osteoconductivity, and osteoinductive capacity, has shown broad prospects in the treatment of large-scale bone defects and bone regeneration. The angiogenesis process of TEB and bone defect are extremely complex, requiring the participation of seed cells and various growth factors produced by cells. Mesenchymal stem cells ( MSCs) are readily available, have less ethical controversy and low immunogenicity, and have the ability of osteogenic and angiogenic differentiation. It has been used as a new method to repair bone defects, which can overcome the shortcomings of the existing treatment method and improve the clinical treatment effect. AMP-activated protein kinase ( AMPK) is an important molecule that regulates cell energy homeostasis and a variety of metabolism-related hormones in eukaryotes. It can be activated by many pathways to play a physiological regulatory role. In recent years, studies have found that it is related to physiological processes of bone regeneration and bone microenvironment formation. It exerts an osteogenic effect by acting on MSCs, osteoblasts, osteoclasts, and angiogenesis. Many researchers have used AMPK and MSCs in combination to treat regeneration and repair of bone injury, which has a positive effect on TEB in promoting bone regeneration. In addition, this article also concludes that AMPK is involved in bone regeneration, which may be related to signal pathways such as reactive oxygen species, autophagy, and silent information regulator l. This paper reviews the research and mechanism of AMPK in TEB promoting bone regeneration, aiming to provide theoretical basis and new ideas for bone defect repair, targeted therapy of bone regeneration and related molecular mechanisms. [ABSTRACT FROM AUTHOR]

BACKGROUND: Bionic porous scaffolds used in bone tissue engineering requires extracellular matrix-like nanofibrous and connected macroporous structure to effectively support cell implantation, adhesion, proliferation and other behaviors, and promote tissue regeneration. OBJECTIVE: To summarize the research progress in nanorfibrous macroporous scaffold preparation technology for tissue engineering based on the latest relevant research trends. METHODS: The first author searched Web of Science, CNKI and Baidu academic databases to retrieve papers published from 2000 to 2019 with the search terms "bone tissue engineering, nanofibrous, macroporous, scaffolds" in English and Chinese, respectively. Finally, 58 articles were included in result analysis. RESULTS AND CONCLUSION: The scaffolds with nanofibrous structures are fabricated using three strategies, including electrospinning, thermally induced phase separation, and self-assembly process. However, bone scaffold fabricated by a single strategy failed to provide interconnected macropores to simulate the microenvironment in the body, which was necessary for cell migration, growth, differentiation, proliferation, and tissue and organ regeneration. Therefore, it is now of great practical and scientific significance to develop macroporous nanofibrous scaffold using a combination of several strategies. Three-dimensional printing technique can provide precise structure and enables the customization of the internal structure and external shape of the scaffold, which promotes the development of bone tissue engineering technique. [ABSTRACT FROM AUTHOR]

During the life time of the human, modelling and remodeling of the bone maintain a precise and dynamic balance. The material exchange in the bone is coordinated through the cells. Researches have found that bone regeneration is not only through the coordination of the cells, but also through the close connection between exosomes that carry and transfer proteins, lipids, and RNAs, and other tissues. Studies have shown that exosomes from various cell sources are involved in the exchange of intercellular substances and information around bone, which can promote the repair and regeneration various bone cells, and regulate the physical and pathological status of the bone. In this paper, the relationship between exosomes and bone regeneration is briefly described according to the recent research reports of exosomes in bone regeneration. [ABSTRACT FROM AUTHOR]

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Clinically, there has been so far no effective way to repair the bone-missing of large extent due to gash, infection and removal of tumor. The solution of this problem can be assisted by the addition of bioactive substances to substrate materials, because the growth of peripheral tissue and the fiber tissue growing the materials can be induced to the direction of bone-tissue by these biomaterials with bioactive peptides. The peptide Arg-Gly-Asp is the point between the integrin which comes from membrane and the ligand. In certain cases, the artificially synthesized RGD can be competitively combined with the integrin on cell surface, and outer-cell information is transmitted into cells, which will cause a series of physiological changes in cells. Presently, it is reported that the RGD has the ability to induce the growth of osteoblasts, restrain the adhesion between osteoclasts and substrates. This paper reviews and introduces the progress made with the work of RGD-inducing bone regeneration.

The paper deals with quantitative study of bone healing in goat after unilateral oblique osteotomy of the mandibular ramus. Bone histomorphometry combined with tetracycline bone labelling and gamma monophoton absorptiometry were used to assess the rate of the new bone formation and its degree of mineralization during the healing process. The result showed that if the articular capsule and the lateral pterygoid muscle were remained and attached, the quantity of new trabaculae and the rate of bone healing in the inferior part of proximal fragment were less than those in the superior part (P < 0.05). There was a bone healing delay in the inferior part of proximal fragment.

BACKGROUND: Some studies have shown that basic fibroblast growth factor can promote the proliferation and osteogenic differentiation of mesenchymal stem cells. OBJECTIVE: To compare the ability of acellular bone matrix/chitosan scaffold combined with basic fibroblast growth factor in repairing rabbit femoral defect. METHODS: The acellular bone matrix/chitosan scaffolds were prepared by fusion blending and freeze-drying method, and the acellular bone matrix/chitosan scaffold loaded with basic fibroblast growth factor was prepared by immersion method. Mouse embryonic osteoblasts MC3T3-E1 were seeded on the surface of the two scaffolds for cell proliferation, cell adhesion and osteogenic gene detection. Cells cultured alone served as control. Bone defect models with a diameter of 5 mm were made in bilateral distal femurs using thirty-six 6-month-old New Zealand white rabbits and randomly divided into three groups by drawing lots. The blank group was not intervened. The simple composite scaffold and growth factor + composite scaffold groups were implanted with acellular bone matrix/chitosan scaffold and acellular bone matrix/chitosan scaffold loaded with basic fibroblast growth factor for X-ray and histological examination. RESULTS AND CONCLUSION: (1) Within 1-11 days of culture, the cell proliferation of basic fibroblast growth factor/acellular bone matrix/chitosan scaffold group was faster than that of the acellular bone matrix/chitosan scaffold group (P < 0.05), and that of the acellular bone matrix/chitosan scaffold group was faster than that of the control group (P < 0.05). (2) After 4 days of co-culture with the scaffold, the mRNA expressions of type I collagen, osteocalcin, osteopontin and Runx2 were higher in the cells in basic fibroblast growth factor/acellular bone matrix/chitosan scaffold group cultured for 4 and 7 days than those of acellular bone matrix/chitosan scaffold group (P < 0.05), and the mRNA expression of alkaline phosphatase was higher than that of acellular bone matrix/chitosan scaffold group after 7 days of culture (P < 0.05). (3) Scanning electron microscopy showed that the scaffolds of the two groups supported the adhesion of MC3T3-E1 cells after 7 days of co-culture. (4) X-ray film of animal experiment showed that there was no obvious bone repair in the blank group at 12 weeks after operation; new bone formation could be seen at 8 weeks after operation in the simple composite scaffold group, and obvious new bone formation could be seen at 12 weeks after operation; new bone formation could be seen at 4 weeks after operation in the cytokine + composite scaffold group, and the bone defect site was almost completely repaired at 12 weeks after operation (5) Hematoxylin staining and Masson staining showed that a large amount of fibrous tissue could be seen in the blank group at 12 weeks after operation; a large amount of new bone formation could be seen in the two scaffold groups, in which the area and maturity of new bone formation in the growth factor + composite scaffold group were higher than those in the simple composite scaffold group. (6) The results showed that the acellular bone matrix/chitosan composite scaffold loaded with basic fibroblast growth factor is an ideal bone tissue repair material, which can promote bone formation. [ABSTRACT FROM AUTHOR]

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

BACKGROUND: Nano-hydroxyapatite/polyamide 66 composite (n-HA/PA66) has good biocompatibility, osteoinduction, osteoconductivity and osteogenesis. It is widely used in clinical fracture healing, spinal fusion, and other bone repair. OBJECTIVE: To observe the effect of n-HA/PA66 filling combined with locking plate in the treatment of fibrous dysplasia of femoral bone. METHODS: From May 2015 to May 2018, 15 patients with fibrous dysplasia of bone were admitted to Xingtai People’s Hospital Affiliated to Hebei Medical University. There were 4 males and 11 females, aged 16-58 years. The lesions were all located in the femur. They were all treated with n-HA/PA66 filling combined with locking plate. The patients were followed up for 18-40 months. Imaging examination (X-ray and CT scan) was carried out to evaluate the bone healing. Musculoskeletal Tumor Society (MSTS) score and Harris score were used to assess the functional recovery of patients after operation. RESULTS AND CONCLUSION: (1) X-ray films showed that there was a clear boundary between the transplanted bone and the host bone immediately after the operation. At 3 months after the operation, the transplanted bone was replaced partly by crawling. At 6 months, new bone formation was obvious. At 9-12 months, new bone formed completely. The transplanted bone was basically catabolized. At 18 months, the new bone was completely integrated with the host bone. The boundary between the new bone and the host bone disappeared. New bone and host bone are connected by direct trabecula. (2) At the last follow-up, CT images showed that the local lesions were eliminated; no recurrence or metastasis occurred; and the grafts healed completely. The G/N ratio was 0.78±0.09. (3) At the last follow-up, 15 patients’ pain all disappeared, MSTS score was 28.1±0.7. Harris score was 94.3. Daily physical activity was restored. (4) n-HA/PA66 composite material has obvious osteogenic effect on the bone defect caused by the removal of fibrous dysplasia. Locking plate fixation can make patients move early and obtain good postoperative function. [ABSTRACT FROM AUTHOR]

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Bone graft material is not only a simple scaffold frame, but also a material with the potential to induce cells grow and differentiate into osteoblasts. The material with excellent bone induction properties can accelerate the healing of bone defect, thus repair the large area of bone defect successfully. Currently, plenty of researches regarding the bone induction in bone graft material have been reported, how to maximize the material osteoinductive potential, and to take advantage of these biological materials to produce the next generation of innovative biological material, is the current concerns. In this paper, a review is made on the bone induction properties of several kinds of bone substitutes.

Copyright of Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu is the property of Chinese Journal of Tissue Engineering Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)