Human duodenal organoid-derived monolayers serve as a suitable barrier model for duodenal tissue

被引:14
|
作者
Weiss, Franziska [1 ]
Holthaus, David [2 ]
Kraft, Martin [2 ]
Klotz, Christian [2 ]
Schneemann, Martina [1 ]
Schulzke, Joerg D. [1 ]
Krug, Susanne M. [1 ]
机构
[1] Charite Univ Med Berlin, Clin Physiol Nutr Med, D-12203 Berlin, Germany
[2] Robert Koch Inst, Dept Infect Dis, Unit 16, Mycot & Parasit Agents & Mycobacteria, Berlin, Germany
关键词
barrier function; Caco-2; cells; duodenum; organoids; tight junction; EPITHELIAL STEM-CELLS; TIGHT JUNCTION; CULTURE-SYSTEM; IN-VITRO; TRICELLULIN; EXPRESSION; CLAUDIN-2; EXPANSION;
D O I
10.1111/nyas.14804
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Usually, duodenal barriers are investigated using intestinal cell lines like Caco-2, which in contrast to native tissue are limited in cell-type representation. Organoids can consist of all intestinal cell types and are supposed to better reflect the in vivo situation. Growing three-dimensionally, with the apical side facing the lumen, application of typical physiological techniques to analyze the barrier is difficult. Organoid-derived monolayers (ODMs) were developed to overcome this. After optimizing culturing conditions, ODMs were characterized and compared to Caco-2 and duodenal tissue. Tight junction composition and appearance were analyzed, and electrophysiological barrier properties, like paracellular and transcellular barrier function and macromolecule permeability, were evaluated. Furthermore, transcriptomic data were analyzed. ODMs had tight junction protein expression and paracellular barrier properties much more resembling the originating tissue than Caco-2. Transcellular barrier was similar between ODMs and native tissue but was increased in Caco-2. Transcriptomic data showed that Caco-2 expressed fewer solute carriers than ODMs and native tissue. In conclusion, while Caco-2 cells differ mostly in transcellular properties, ODMs reflect trans- and paracellular properties of the originating tissue. If cultured under optimized conditions, ODMs possess reproducible functionality, and the variety of different cell types makes them a suitable model for human tissue-specific investigations.
引用
收藏
页码:155 / 167
页数:13
相关论文
共 50 条
  • [21] An organoid-derived bronchioalveolar model for SARS-CoV-2 infection of human alveolar type II-like cells
    Lamers, Mart M.
    van der Vaart, Jelte
    Knoops, Kevin
    Riesebosch, Samra
    Breugem, Tim, I
    Mykytyn, Anna Z.
    Beumer, Joep
    Schipper, Debby
    Bezstarosti, Karel
    Koopman, Charlotte D.
    Groen, Nathalie
    Ravelli, Raimond B. G.
    Duimel, Hans Q.
    Demmers, Jeroen A. A.
    Verjans, Georges M. G. M.
    Koopmans, Marion P. G.
    Muraro, Mauro J.
    Peters, Peter J.
    Clevers, Hans
    Haagmans, Bart L.
    EMBO JOURNAL, 2021, 40 (05)
  • [22] Single-cell transcriptomics of human organoid-derived enteroendocrine cell populations from the small intestine
    Smith, Christopher A.
    Lu, Van B.
    Bakar, Rula Bany
    Miedzybrodzka, Emily
    Davison, Adam
    Goldspink, Deborah
    Reimann, Frank
    Gribble, Fiona M.
    JOURNAL OF PHYSIOLOGY-LONDON, 2024,
  • [23] An Organoid-derived Cell Layer as an in vitro Model for US-mediated Drug Delivery Studies
    Turcanu, Mihnea, V
    Cochran, Sandy
    Moldovan, Alexandru C.
    Vlatakis, Stavros
    Vllasaliu, Driton
    Thanou, Maya
    Nathke, Inke
    PROCEEDINGS OF THE 2020 IEEE INTERNATIONAL ULTRASONICS SYMPOSIUM (IUS), 2020,
  • [24] Human metapneumovirus infection of organoid-derived human bronchial epithelium represents cell tropism and cytopathology as observed in in vivo models
    Ribo-Molina, Pau
    van Nieuwkoop, Stefan
    Mykytyn, Anna Z.
    van Run, Peter
    Lamers, Mart M.
    Haagmans, Bart L.
    Fouchier, Ron A. M.
    van den Hoogen, Bernadette G.
    MSPHERE, 2024, 9 (02)
  • [25] Human intestinal organoid-derived PDGFRα plus mesenchymal stroma enables proliferation and maintenance of LGR4+epithelial stem cells
    Chen, Junlong
    Horiuchi, Shinichiro
    Kuramochi, So
    Kawasaki, Tomoyuki
    Kawasumi, Hayato
    Akiyama, Saeko
    Arai, Tomoki
    Morinaga, Kenichi
    Kimura, Tohru
    Kiyono, Tohru
    Akutsu, Hidenori
    Ishida, Seiichi
    Umezawa, Akihiro
    STEM CELL RESEARCH & THERAPY, 2024, 15 (01)
  • [26] Use of human tissue stem cell-derived organoid cultures to model enterohepatic circulation
    Blutt, Sarah E.
    Crawford, Sue E.
    Bomidi, Carolyn
    Zeng, Xi-Lei
    Broughman, James R.
    Robertson, Matthew
    Coarfa, Cristian
    Tessier, Mary Elizabeth M.
    Savidge, Tor
    Hollinger, F. Blaine
    Curley, Steven A.
    Donowitz, Mark
    Estes, Mary K.
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2021, 321 (03): : G270 - G279
  • [27] Organoid-derived human retinal progenitor cells promote early dedifferentiation of M?ller glia in Royal College of Surgeons rats
    Guo, Qiang
    Zeng, Yu-Xiao
    Huang, Shu-Dong
    Zou, Ting
    Yin, Zheng-Qin
    INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, 2023, 16 (04) : 483 - 498
  • [28] Human intestinal organoid-derived PDGFRα + mesenchymal stroma enables proliferation and maintenance of LGR4 + epithelial stem cells
    JunLong Chen
    Shinichiro Horiuchi
    So Kuramochi
    Tomoyuki Kawasaki
    Hayato Kawasumi
    Saeko Akiyama
    Tomoki Arai
    Kenichi Morinaga
    Tohru Kimura
    Tohru Kiyono
    Hidenori Akutsu
    Seiichi Ishida
    Akihiro Umezawa
    Stem Cell Research & Therapy, 15
  • [29] An organoid model derived from human adipose stem/progenitor cells to study adipose tissue physiology
    Mandl, Markus
    Viertler, Hans P.
    Hatzmann, Florian M.
    Brucker, Camille
    Grossmann, Sonja
    Waldegger, Petra
    Rauchenwald, Tina
    Mattesich, Monika
    Zwierzina, Marit
    Pierer, Gerhard
    Zwerschke, Werner
    ADIPOCYTE, 2022, 11 (01) : 164 - 174
  • [30] Retinoic acid promotes barrier functions in human iPSC-derived intestinal epithelial monolayers
    Yamada, Shigeru
    Kanda, Yasunari
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2019, 140 (04) : 337 - 344