Using Avian Skin Explants to Study Tissue Patterning and Organogenesis.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
15 09 2023
Historique:
medline: 3 10 2023
pubmed: 2 10 2023
entrez: 2 10 2023
Statut: epublish

Résumé

The developing avian skin during embryogenesis is a unique model that can provide valuable insights into tissue patterning. Here three variations on skin explant cultures to examine different aspects of skin development are described. First, ex vivo organ cultures and manipulations offer researchers opportunities to observe and study the development of feather buds directly. Skin explant culture can grow for 7 days enabling direct analysis of cellular behavior and 4D imaging at intervals during this growth period. This also allows for physical and molecular manipulations of culture conditions to visualize tissue response. For example, growth factor-coated beads can be applied locally to induce changes in feather patterning in a limited area. Alternatively, viral transduction can be delivered globally in the culture media to up or downregulate gene expression. Second, the skin recombination protocol allows researchers to investigate tissue interactions between the epidermis and mesenchyme that are derived from different skin regions, different life stages, or different species. This affords an opportunity to test the time window in which the epithelium is competent to respond to signals and its ability to form different skin appendages in response to signals from different mesenchymal sources. Third, skin reconstitution using dissociated dermal cells overlaid with intact epithelium resets skin development and enables the study of the initial processes of periodic patterning. This approach also enhances our ability to manipulate gene expression among the dissociated cells before creating the reconstituted skin explant. This paper provides the three culture protocols and exemplary experiments to demonstrate their utility.

Identifiants

pubmed: 37782100
doi: 10.3791/65580
doi:

Types de publication

Journal Article Video-Audio Media Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAMS NIH HHS
ID : R37 AR060306
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR047364
Pays : United States

Auteurs

Tingxin Jiang (T)

Department of Pathology, Keck School of Medicine of University of Southern California; tjiang@usc.edu.

Maeve Secor (M)

Molecular and Computational Biology, University of Southern California.

Rusty Lansford (R)

Department of Radiology, Keck School of Medicine of University of Southern California.

Randall B Widelitz (RB)

Department of Pathology, Keck School of Medicine of University of Southern California.

Cheng Ming Chuong (CM)

Department of Pathology, Keck School of Medicine of University of Southern California.

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Classifications MeSH