Engineered three-dimensional rabbit oral epithelial–mesenchymal–muscular hybrid sheets

Shigeki Yamane , Kazunari Higa , Takashi Umezawa , Masamitsu Serikawa , Jun Shimazaki , Shinichi Abe

International Journal of Oral Science ›› 2016, Vol. 8 ›› Issue (3) : 145 -154.

PDF
International Journal of Oral Science ›› 2016, Vol. 8 ›› Issue (3) : 145 -154. DOI: 10.1038/ijos.2016.16
Article

Engineered three-dimensional rabbit oral epithelial–mesenchymal–muscular hybrid sheets

Author information +
History +
PDF

Abstract

Laboratory-made sheets of the cells from the inside of the mouth could help treat oral muscular defects. Shigeki Yamane and colleagues from Tokyo Dental College, Japan, isolated different kinds of rabbit cells from the mucous membrane that lines the mouth. They then fabricated layered sheets that contained all three cell types: epithelial, mesenchymal, and muscular. The researchers studied the expression of proteins that are essential for maintaining this structure and found that, on a molecular level, the tissues of the engineered sheets closely resembled those found inside the oral cavity. The cells also had the capacity to proliferate after grafting. Similar constructs made of human cells could offer a path toward regenerative therapies for people with muscle problems in the tongue or pharynx who have trouble swallowing or chewing.

Keywords

mesenchymal stem cell / multi-differentiation / myoblast / oral mucosa / three-dimensional culture

Cite this article

Download citation ▾
Shigeki Yamane, Kazunari Higa, Takashi Umezawa, Masamitsu Serikawa, Jun Shimazaki, Shinichi Abe. Engineered three-dimensional rabbit oral epithelial–mesenchymal–muscular hybrid sheets. International Journal of Oral Science, 2016, 8(3): 145-154 DOI:10.1038/ijos.2016.16

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Chida K, Nagase T, Yakuwa S. A case of buccal mucosa carcinoma with cheek reconstruction using forehead flap full-thickness defect. Practica Otologica Suppl, 2011, 130: 85-89.

[2]

Futrell JW, Johns ME, Edgerton MT. Platysma myocutaneous flap for intraoral reconstruction. Am J Surg, 1978, 136(4): 504-507.

[3]

Imai T, Matsuura K, Asada Y. [A case of buccal mucosa carcinoma reconstructed by platysma myocutaneous flap. J Jpn Soc Head Neck Surg, 2012, 22: 187-192.

[4]

Hamada Y, Sato J. A study of recovery of oral and maxillofacial function by surgical reconstruction after ablation of oral malignant tumors: postoperative conversational ability after resection involving the tongue, mouth floor, and mandible. Jpn J Oral Maxillofac Surg, 1998, 44(11): 852-865.

[5]

Hanazawa H, Konno A. Now and future of functional reconstruction of tongue and otral floor. Head Neck Cancer, 1998, 24(3): 393-402.

[6]

Euchi Y, Hamaguchi M, Kogo M. Evaluation of reconstruction of soft tissue following surgery for oral cancer using articulation test of pronunciation and conversational intelligibility. Head Neck Cancer, 2003, 29(1): 111-117.

[7]

Ohki T, Yamato M, Murakami D. Treatment of oesophageal ulcerations using endoscopic transplantation of tissue-engineered autologous oral mucosal epithelial cell sheets in a canine model. Gut, 2006, 55(12): 1704-1710.

[8]

Takagi R, Murakami D, Kondo M. Fabrication of human oral mucosal epithelial cell sheets for treatment of esophageal ulceration by endoscopic submucosal dissection. Gastrointest Endosc, 2010, 72(6): 1253-1259.

[9]

Takagi R, Yamato M, Murakami D. Preparation of keratinocyte culture medium for the clinical applications of regenerative medicine. J Tissue Eng Regen Med, 2011, 5(4): e63-e73.

[10]

Shimazaki J, Higa K, Kato N. Barrier function of cultivated limbal and oral mucosal epithelial cell sheets. Invest Ophthalmol Vis Sci, 2009, 50(12): 5672-5680.

[11]

Higa K, Shimmura S, Kato N. Proliferation and differentiation of transplantable rabbit epithelial sheets engineered with or without an amniotic membrane carrier. Invest Ophthalmol Vis Sci, 2007, 48(2): 597-604.

[12]

Kuroda Y, Kitada M, Wakao S. Unique multipotent cells in adult human mesenchymal cell populations. Proc Natl Acad Sci USA, 2010, 107(19): 8639-8643.

[13]

Qu Z, Balkir L, van Deutekom JC. Development of approaches to improve cell survival in myoblast transfer therapy. J Cell Biol, 1998, 142(5): 1257-1267.

[14]

Qu-Petersen Z, Deasy B, Jankowski R. Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration. J Cell Biol, 2002, 157(5): 851-864.

[15]

Rouger K, Fornasari B, Armengol V. Progenitor cell isolation from muscle-derived cells based on adhesion properties. J Histochem Cytochem, 2007, 55(6): 607-618.

[16]

Marynka-Kalmani K, Treves S, Yafee M. The lamina propria of adult human oral mucosa harbors a novel stem cell population. Stem Cells, 2010, 28(5): 984-995.

[17]

Widera D, Zander C, Heidbreder M. Adult palatum as a novel source of neural crest-related stem cells. Stem Cells, 2009, 27(8): 1899-1910.

[18]

Satake Y, Higa K, Matsumura S. Establishment of isolation and culture procedure of multi-differential potent stem cells from oral mucosa non-epithelial tissue. Shikagakuho, 2013, 113(5): 509-515.

[19]

Rantanen J, Hurme T, Lukka R. Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells. Lab Invest, 1995, 72(3): 341-347.

[20]

Schultz E. Satellite cell proliferative compartments in growing skeletal muscles. Dev Biol, 1996, 175(1): 84-94.

[21]

Li L, Fukunaga-Kalabis M, Herlyn M. The three-dimensional human skin reconstruct model: a tool to study normal skin and melanoma progression. J Vis Exp, 2011, 3(54): 2937.

[22]

Killat J, Reimers K, Choi CY. Cultivation of keratinocytes and fibroblasts in a three-dimensional bovine collagen-elastin matrix (Matriderm) and application for full thickness wound coverage in vivo. Int J Mol Sci, 2013, 14(7): 14460-14474.

[23]

Rheinwald JG, Green H. Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. Cell, 1975, 6(3): 331-343.

[24]

Barrandon Y, Green H. Cell size as a determinant of the clone-forming ability of human keratinocytes. Proc Natl Acad Sci USA, 1985, 82(16): 5390-5394.

[25]

Smola H, Thiekötter G, Fusenig NE. Mutual induction of growth factor gene expression by epidermal-dermal cell interaction. J Cell Biol, 1993, 122(2): 417-429.

[26]

Ikuta S, Sekino N, Hara T. Mouse epidermal keratinocytes in three-dimensional organotypic coculture with dermal fibroblasts form a stratified sheet resembling skin. Biosci Biotechnol Biochem, 2006, 70(11): 2669-2675.

[27]

Ravindran S, Song Y, George A. Development of three-dimensional biomimetic scaffold to study epithelial-mesenchymal interactions. Tissue Eng Part A, 2010, 16(1): 327-342.

[28]

Miyashita H, Shimmura S, Higa K. A novel NIH/3T3 duplex feeder system to engineer corneal epithelial sheets with enhanced cytokeratin 15-positive progenitor populations. Tissue Eng Part A, 2008, 14(7): 1275-1282.

[29]

Shimizu T, Sekine H, Yang J. Polysurgery of cell sheet grafts overcomes diffusion limits to produce thick, vascularized myocardial tissues. FASEB J, 2006, 20(6): 708-710.

[30]

Zammit PS, Partridge TA, Yablonka-Reuveni Z. The skeletal muscle satellite cell: the stem cell that came in from the cold. J Histochem Cytochem, 2006, 54(11): 1177-1191.

[31]

Seale P, Ishibashi J, Scimè A. Pax7 is necessary and sufficient for the myogenic specification of CD45+:Sca1+ stem cells from injured muscle. PLoS Biol, 2004, 2(5): E130.

[32]

Beauchamp JR, Heslop L, Yu DS. Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells. J Cell Biol, 2000, 151(6): 1221-1234.

[33]

Garzon I, Serrato D, Roda O. In vitro cytokeratin expression profiling of human oral mucosa substitutes developed by tissue engineering. Int J Artif Organs, 2009, 32(10): 711-719.

[34]

Calvi LM, Adams GB, Weibrecht KW. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature, 2003, 425(6960): 841-846.

[35]

Zhang J, Niu C, Ye L. Identification of the haematopoietic stem cell niche and control of the niche size. Nature, 2003, 425(6960): 836-841.

[36]

Bustos RH, Suesca E, Millán D. Real-time quantification of proteins secreted by artificial connective tissue made from uni- or multidirectional collagen I scaffolds and oral mucosa fibroblasts. Anal Chem, 2014, 86(5): 2421-2428.

[37]

Igarashi T, Shimmura S, Yoshida S. Isolation of oral epithelial progenitors using collagen IV. Oral Dis, 2008, 14(5): 413-418.

[38]

Macfelda K, Kapeller B, Wilbacher I. Behavior of cardiomyocytes and skeletal muscle cells on different extracellular matrix components—relevance for cardiac tissue engineering. Artif Organs, 2007, 31(1): 4-12.

[39]

Boonen KJ, Rosaria-Chak KY, Baaijens FP. Essential environmental cues from the satellite cell niche: optimizing proliferation and differentiation. Am J Physiol Cell Physiol, 2009, 296(6): C1338-C1345.

[40]

Wilschut KJ, Haagsman HP, Roelen BA. Extracellular matrix components direct porcine muscle stem cell behavior. Exp Cell Res, 2010, 316(3): 341-352.

AI Summary AI Mindmap
PDF

133

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/