Construction of Human Three-Dimensional Lung Model Using Layer-by-Layer Method

被引:0
|
作者
Akamatsu, Yukako [1 ,2 ]
Akagi, Takami [3 ]
Sumitomo, Tomoko [1 ]
Takahara, Yuki [1 ,4 ]
Akiyama, Shigehisa [2 ]
Kawabata, Shigetada [1 ,5 ,6 ]
Akashi, Mitsuru [3 ,7 ]
机构
[1] Osaka Univ, Grad Sch Dent, Dept Oral & Mol Microbiol, Osaka, Japan
[2] Osaka Univ, Dent Hosp, Div Special Care Dent, Osaka, Japan
[3] Osaka Univ, Bldg Block Sci Joint Res Chair, Grad Sch Frontier Biosci, Osaka, Japan
[4] Osaka Univ, Grad Sch Dent, Dept Fixed Prosthodont, Osaka, Japan
[5] Osaka Univ, Ctr Infect Dis Educ & Res, Osaka, Japan
[6] Osaka Univ, Grad Sch Dent, Dept Oral & Mol Microbiol, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan
[7] Osaka Univ, Bldg Block Sci Joint Res Chair, Grad Sch Frontier Biosci, 1-3 Yamadaoka, Suita, Osaka 5650871, Japan
关键词
cell coating technique; 3D lung model; layer-by-layer; IN-VITRO MODEL; CELL-LINE; CALU-3; CULTURE; FABRICATION; SURFACTANT; JUNCTIONS; RELEASE; ALPHA-5; TISSUES;
D O I
10.1089/ten.tec.2022.0184
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The respiratory tract is one of the frontline barriers for biological defense. Lung epithelial intercellular adhesions provide protection from bacterial and viral infections and prevent invasion into deep tissues by pathogens. Dysfunction of lung epithelial intercellular adhesion caused by pathogens is associated with development of several diseases, such as acute respiratory distress syndrome, pneumonia, and asthma. To elucidate the pathological mechanism of respiratory infections, two-dimensional cell cultures and animal models are commonly used, although are not useful for evaluating host specificity or human biological response. With the rapid progression and worldwide spread of severe acute respiratory syndrome coronavirus-2, there is increasing interest in the development of a three-dimensional (3D) in vitro lung model for analyzing interactions between pathogens and hosts. However, some models possess unclear epithelial polarity or insufficient barrier functions and need the use of complex technologies, have high cost, and long cultivation terms. We previously reported about the fabrication of 3D cellular multilayers using a layer-by-layer (LbL) cell coating technique with extracellular matrix protein, fibronectin (FN), and gelatin (G). In the present study, such a LbL cell coating technique was utilized to construct a human 3D lung model in which a monolayer of the human lower airway epithelial adenocarcinoma cell line Calu-3 cells was placed on 3D-cellular multilayers composed of FN-G-coated human primary pulmonary fibroblast cells. The 3D lung model thus constructed demonstrated an epithelial-fibroblast layer that maintained uniform thickness until 7 days of incubation. Moreover, expressions of E-cadherin, ZO-1, and mucin in the epithelial layer were observed by immunohistochemical staining. Epithelial barrier integrity was evaluated using transepithelial electrical resistance values. The results indicate that the present constructed human 3D lung model is similar to human lung tissues and also features epithelial polarity and a barrier function, thus is considered useful for evaluating infection and pathological mechanisms related to pneumonia and several pathogens. Impact statementA novel in vitro model of lung tissue was established.Using a layer-by-layer cell coating technique, a three-dimensional cultured lung model was constructed.The present novel model was shown to have epithelial polarity and chemical barrier functions.This model may be useful for investigating interaction pathogens and human biology.
引用
收藏
页码:95 / 102
页数:8
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