Non-Animal Models in Dermatological Research

被引:34
作者
Dellambra, Elena [1 ,4 ]
Odorisio, Teresa [1 ,4 ]
D'Arcangelo, Daniela [2 ,4 ]
Failla, Cristina M. [3 ,4 ]
Facchiano, Antonio [2 ,4 ]
机构
[1] IRCCS, IDI, Lab Mol & Cell Biol, Rome, Italy
[2] IRCCS, IDI, Lab Mol Oncol, Rome, Italy
[3] IRCCS, IDI, Lab Expt Immunol, Via Moriti di Creta 104, I-00167 Rome, Italy
[4] IRCCS, IDI, Working Grp ALMA, Rome, Italy
关键词
IN-VITRO MODEL; ADVANCED GLYCATION ENDPRODUCTS; HUMAN-MELANOMA PROGRESSION; HUMAN SKIN EQUIVALENT; DIABETIC FOOT ULCERS; WOUND-HEALING MODEL; HUMAN PROTEIN ATLAS; HUMAN CELL-LINES; TEST H-CLAT; RECONSTRUCTED-SKIN;
D O I
10.14573/altex.1808022
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Despite being widely used for basic and preclinical studies in dermatology, available animal models only partly recapitulate human skin features, often leading to disappointing outputs when preclinical results are translated to the clinic. Therefore, the need to develop alternative, non-animal models is widely recognized to more closely recapitulate human skin pathophysiology and to address the pressing ethical demand to reduce the number of animals used for research purposes, following the globally accepted 3Rs principle (Replacement, Reduction, and Refinement). Skin is the outermost organ of the body, and is, as such, easily accessible. Different skin cell types can be propagated in vitro, and skin can be reconstructed for therapeutic transplantation as well as for in vitro modelling of pathophysiological conditions. Bio-engineered skin substitutes have been developed and have evolved from elementary to complex systems, more and more closely resembling complete skin architecture and biological responses. In silico analyses take advantage of the huge amount of data already available from human studies to identify and model molecular pathways involved in skin pathophysiology without further animal testing. The present review recapitulates the available non-animal models for dermatological research and sheds light on their prospective technological evolution.
引用
收藏
页码:177 / 202
页数:26
相关论文
共 281 条
  • [11] Intrahepatic Xenograft of Cutaneous T-Cell Lymphoma Cell Lines A Useful Model for Rapid Biological and Therapeutic Evaluation
    Andrique, Laetitia
    Poglio, Sandrine
    Prochazkova-Carlotti, Martina
    Kadin, Marshall Edward
    Giese, Alban
    Idrissi, Yamina
    Beylot-Barry, Marie
    Merlio, Jean-Philippe
    Chevret, Edith
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2016, 186 (07) : 1775 - 1785
  • [12] [Anonymous], 2017, BTS BIOENG, DOI DOI 10.3390/BIOENGINEERING4030066
  • [13] Development of an in vitro skin sensitization test using human cell lines: The human Cell Line Activation Test (h-CLAT) I. Optimization of the h-CLAT protocol
    Ashikaga, T
    Yoshida, Y
    Hirota, M
    Yoneyama, K
    Itagaki, H
    Sakaguchi, H
    Miyazawa, M
    Ito, Y
    Suzuki, H
    Toyoda, H
    [J]. TOXICOLOGY IN VITRO, 2006, 20 (05) : 767 - 773
  • [14] RECONSTRUCTION OF SIMPLIFIED SKIN - CONTROL OF FABRICATION
    ASSELINEAU, D
    PRUNIERAS, M
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 1984, 111 : 219 - 222
  • [15] Skin and hair on-a-chip: in vitro skin models versus ex vivo tissue maintenance with dynamic perfusion
    Atac, Beren
    Wagner, Ilka
    Horland, Reyk
    Lauster, Roland
    Marx, Uwe
    Tonevitsky, Alexander G.
    Azar, Reza P.
    Lindner, Gerd
    [J]. LAB ON A CHIP, 2013, 13 (18) : 3555 - 3561
  • [16] A systems approach reveals distinct metabolic strategies among the NCI-60 cancer cell lines
    Aurich, Maike K.
    Fleming, Ronan M. T.
    Thiele, Ines
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2017, 13 (08) : e1005698
  • [17] Animal models of skin disease for drug discovery
    Avci, Pinar
    Sadasivam, Magesh
    Gupta, Asheesh
    De Melo, Wanessa C. M. A.
    Huang, Ying-Ying
    Yin, Rui
    Chandran, Rakkiyappan
    Kumar, Raj
    Otufowora, Ayodeji
    Nyame, Theodore
    Hamblin, Michael R.
    [J]. EXPERT OPINION ON DRUG DISCOVERY, 2013, 8 (03) : 331 - 355
  • [18] Ayata Raif Eren, 2014, Biores Open Access, V3, P197, DOI 10.1089/biores.2014.0022
  • [19] In Silico Analysis Validates Proteomic Findings of Formalin-fixed Paraffin Embedded Cutaneous Squamous Cell Carcinoma Tissue
    Azimi, Ali
    Kaufman, Kimberley L.
    Ali, Marina
    Kossard, Steven
    Fernandez-Penas, Pablo
    [J]. CANCER GENOMICS & PROTEOMICS, 2016, 13 (06) : 453 - 465
  • [20] The HtrA1 serine protease is down-regulated during human melanoma progression and represses growth of metastatic melanoma cells
    Baldi, A
    De Luca, A
    Morini, M
    Battista, T
    Felsani, A
    Baldi, F
    Catricalà, C
    Amantea, A
    Noonan, DM
    Albini, A
    Natali, PG
    Lombardi, D
    Paggi, MG
    [J]. ONCOGENE, 2002, 21 (43) : 6684 - 6688