scholarly journals Injectable adipose tissue combined with stem cells for soft-tissue augmentation: A pilot study for dental applications

2016 ◽  
Vol 11 (4) ◽  
pp. 377-386
Author(s):  
Li-Ting Li ◽  
Kuang-Ta Yao ◽  
Shou-Cheng Teng ◽  
Tiffany P. Sun ◽  
Ching-Kuo Chen ◽  
...  
2017 ◽  
Vol 105 (6) ◽  
pp. 1756-1764 ◽  
Author(s):  
Qiu-Wen Tan ◽  
Yi Zhang ◽  
Jing-Cong Luo ◽  
Di Zhang ◽  
Bin-Jun Xiong ◽  
...  

2021 ◽  
Vol 11 (5) ◽  
pp. 430
Author(s):  
Hytham N. Fageeh ◽  
Shilpa Bhandi ◽  
Mohammed Mashyakhy ◽  
Ahmed Al Kahtani ◽  
Zahi Badran ◽  
...  

Autogenous gingival grafts used for root coverage or gingival augmentation procedures often result in donor site morbidity. Living cellular constructs as an exogenous alternative have been proven to be associated with lower morbidity. With the available background information, the present study aims to assess if quercetin-induced living cell constructs, derived from dental pulp stem cells, have the potential to be applied as a tool for soft tissue augmentation. The characterized dental pulp stem cells (positive for CD73, CD90, and negative for CD34, HLA-DR) were expanded in Dulbecco’s Modified Eagle’s medium (DMEM) supplemented with 10 mM quercetin. The handling properties of the quercetin-induced dental pulp stem cell constructs were assessed by visual, and tactile sensation. A microscopic characterization using hematoxylin and eosin staining, and qRT-PCR-based analysis for stemness-associated genes (OCT4, NANOG, SOX2, and cMyc) was also performed. Dental pulp stem cells without quercetin administration were used as the control. Dental pulp stem cell constructs induced by quercetin easily detached from the surface of the plate, whereas there was no formation in the control cells. It was also simple to transfer the induced cellular construct on the flattened surface. Microscopic characterization of the constructs showed cells embedded in a tissue matrix. Quercetin also increased the expression of stemness-related genes. The use of quercetin-induced DPSC living constructs for soft tissue augmentation could provide an alternative to autogenous soft tissue grafts to lower patient morbidity and improve esthetic outcomes.


Author(s):  
Lorenzo Tavelli ◽  
Shayan Barootchi ◽  
Jad Majzoub ◽  
Hsun‐Liang Chan ◽  
William V. Giannobile ◽  
...  

2007 ◽  
Vol 342-343 ◽  
pp. 349-352 ◽  
Author(s):  
Jong Won Rhie ◽  
Jin Kyung Song ◽  
Paik Kwon Lee ◽  
Sang Tae Ahn

Alginate was a proven biocompatible biomatrice for cells but it was known not to provide a proper microenvironment needed for the proliferation of cells because of its anionic property, which caused its low affinity for cells. Water-soluble chitosan was well known as wound healing material and it also had cationic property which helped cell-to-matrix adhesion. The purpose of this study is to assess the ability of a chitosan/alginate mixed sponge as a scaffold for preadipocytes to serve as a biological implant for soft tissue augmentation. Chitosan/alginate and calcium alginate sponges were made by lyophilizing of alginate with water-soluble chitosan mixture and with calcium chloride mixture, respectively, and those were observed by SEM. Preadipocytes seeded in those sponges were cultured for 2 weeks. In vivo study was designed that chitosan/alginate sponges with and without preadipocytes were implanted subcutaneously into nude mouse. Chitosan/alginate and calcium alginate sponges which had highly porosity and 50-200㎛ pore size. In the chitosan/alginate sponge, the levels of DNA amount were significantly higher than those in calcium alginate sponge (P<0.05). In both groups, they increased progressively with time. On the in vivo study, it was observed that adipose tissue layer in the margin of chitosan/alginate sponge on the 2 weeks after implantation of nude mouse. On the 8 weeks after implantation, thick layer of adipose tissue and neovascularization were observed in the chitosan/alginate sponge. Consequently, chitosan/alginate sponge provided proper microenvironment to human preadipocyte, increased the cell proliferation and maintained the pore that offered neovascularization, so turned out to be effective form of fat transplantation for soft tissue augmentation and reconstruction.


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