Hydrolyzed eggshell membrane immobilized on phosphorylcholine polymer supplies extracellular matrix environment for human dermal fibroblasts

被引:0
|
作者
Eri Ohto-Fujita
Tomohiro Konno
Miho Shimizu
Kazuhiko Ishihara
Toshihiro Sugitate
Jun Miyake
Kotaro Yoshimura
Kaori Taniwaki
Takashi Sakurai
Yukio Hasebe
Yoriko Atomi
机构
[1] The University of Tokyo,Graduate School of Information Science and Technology
[2] The University of Tokyo,Department of Bioengineering, School of Engineering
[3] The University of Tokyo,Center for NanoBio Integration
[4] The University of Tokyo,Department of Materials Engineering, School of Engineering
[5] The University of Tokyo,Department of Plastic Surgery, Graduate School of Medicine
[6] University of Osaka,Department of Mechanical Science and Bioengineering, Graduate School of Engineering Science
[7] Almado incorporation,Department of Life Science, Graduate School of Arts & Science
[8] The University of Tokyo,Radioisotope Center
[9] The University of Tokyo,undefined
来源
Cell and Tissue Research | 2011年 / 345卷
关键词
Extracellular matrix; Eggshell membrane; Phospholipid polymer; Dermal fibroblasts; Type III collagen; Human;
D O I
暂无
中图分类号
学科分类号
摘要
We have found that a water-soluble alkaline-digested form of eggshell membrane (ASESM) can provide an extracellular matrix (ECM) environment for human dermal fibroblast cells (HDF) in vitro. Avian eggshell membrane (ESM) has a fibrous-meshwork structure and has long been utilized as a Chinese medicine for recovery from burn injuries and wounds in Asian countries. Therefore, ESM is expected to provide an excellent natural material for biomedical use. However, such applications have been hampered by the insolubility of ESM proteins. We have used a recently developed artificial cell membrane biointerface, 2-methacryloyloxyethyl phosphorylcholine polymer (PMBN) to immobilize ASESM proteins. The surface shows a fibrous structure under the atomic force microscope, and adhesion of HDF to ASESM is ASESM-dose-dependent. Quantitative mRNA analysis has revealed that the expression of type III collagen, matrix metalloproteinase-2, and decorin mRNAs is more than two-fold higher when HDF come into contact with a lower dose ASESM proteins immobilized on PMBN surface. A particle-exclusion assay with fixed erythrocytes has visualized secreted water-binding molecules around the cells. Thus, HDF seems to possess an ECM environment on the newly designed PMBN-ASESM surface, and future applications of the ASESM-PMBN system for biomedical use should be of great interest.
引用
收藏
页码:177 / 190
页数:13
相关论文
共 50 条
  • [41] Artificial extracellular matrices support cell growth and matrix synthesis of human dermal fibroblasts in macroporous 3D scaffolds
    van der Smissen, Anja
    Hoffmeister, Peter-Georg
    Friedrich, Nadja
    Watarai, Akira
    Hacker, Michael C.
    Schulz-Siegmund, Michaela
    Anderegg, Ulf
    JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2017, 11 (05) : 1390 - 1402
  • [42] Human Galectins Induce Conversion of Dermal Fibroblasts into Myofibroblasts and Production of Extracellular Matrix: Potential Application in Tissue Engineering and Wound Repair
    Dvorankova, Barbora
    Szabo, Pavol
    Lacina, Lukas
    Gal, Peter
    Uhrova, Jana
    Zima, Tomas
    Kaltner, Herbert
    Andre, Sabine
    Gabius, Hans-Joachim
    Sykova, Eva
    Smetana, Karel, Jr.
    CELLS TISSUES ORGANS, 2011, 194 (06) : 469 - 480
  • [43] Effects of a natural multi-component compound formulation on the growth, morphology and extracellular matrix production of human adult dermal fibroblasts
    Benvenuto, Monica
    Mattera, Rosanna
    Miele, Martino Tony
    Giganti, Maria Gabriella
    Tresoldi, Ilaria
    Albonici, Loredana
    Manzari, Vittorio
    Modesti, Andrea
    Masuelli, Laura
    Bei, Roberto
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2019, 18 (04) : 2639 - 2647
  • [44] INDUCED SYNTHESIS OF THE BETA-INTEGRINS BY RECOMBINANT HUMAN PDGF ENHANCES THE MIGRATORY RESPONSE OF DERMAL HUMAN FIBROBLASTS TO VARIOUS EXTRACELLULAR-MATRIX PROTEINS
    KIRCHBERG, K
    JUNGTAUBL, H
    KNAUB, S
    HEINEN, G
    LANGE, TS
    MEYERINGOLD, W
    PLEWIG, G
    SCHARFFETTERKOCHANEK, K
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 100 (04) : 461 - 461
  • [45] Shotgun proteomics of extracellular matrix in late senescent human dermal fibroblasts reveals a down-regulated fibronectin-centered network
    Cho, Kun
    Yang, Kyeong Eun
    Nam, Soo-Bin
    Lee, Song-I.
    Yeo, Eui-Ju
    Choi, Jong-Soon
    JOURNAL OF ANALYTICAL SCIENCE AND TECHNOLOGY, 2022, 13 (01)
  • [46] Differential Expression of Extracellular Matrix and Immune-associated Genes during radiation-induced Differentiation of human Dermal Fibroblasts In vitro
    Herskind, C.
    Sticht, C.
    Sami, A.
    Giordano, F.
    Wenz, F.
    STRAHLENTHERAPIE UND ONKOLOGIE, 2021, 197 (SUPPL 1) : S208 - S208
  • [47] Extracellular matrix derived peptides induce elastogenesis in primary cultures and transplants of human dermal fibroblasts and clinically improve elasticity and appearance of skin
    Jimenez, F
    Mitts, TF
    Hinek, A
    MATRIX BIOLOGY, 2004, 23 (06) : 404 - 405
  • [48] Shotgun proteomics of extracellular matrix in late senescent human dermal fibroblasts reveals a down-regulated fibronectin-centered network
    Kun Cho
    Kyeong Eun Yang
    Soo-Bin Nam
    Song-I. Lee
    Eui-Ju Yeo
    Jong-Soon Choi
    Journal of Analytical Science and Technology, 13
  • [49] Sphingosylphosphorylcholine on wound healing: Stimulation of fibroblast-embedded collagen gel contraction and upregulation of extracellular matrix protein synthesis in human dermal fibroblasts
    Suhr, K
    Park, J
    Tsuboi, R
    Ogawa, H
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (04) : 632 - 632
  • [50] Artificial extracellular matrix composed of collagen I and sulfated glycosaminoglycans prevents TGFβ1-induced differentiation of human dermal fibroblasts to myofibroblasts
    van der Smissen, A.
    Hintze, V.
    Scharnweber, D.
    Moeller, S.
    Schnabelrauch, M.
    Majok, A.
    Simon, J. C.
    Anderegg, U.
    EXPERIMENTAL DERMATOLOGY, 2012, 21 (03) : e5 - e5