3D culture assays of murine mammary branching morphogenesis and epithelial invasion

Methods Mol Biol. 2015:1189:135-62. doi: 10.1007/978-1-4939-1164-6_10.

Abstract

Epithelia are fundamental tissues that line cavities, glands, and outer body surfaces. We use three-dimensional (3D) embedded culture of primary murine mammary epithelial ducts, called "organoids," to recapitulate in days in culture epithelial programs that occur over weeks deep within the body. Modulating the composition of the extracellular matrix (ECM) allows us to model cell- and tissue-level behaviors observed in normal development, such as branching morphogenesis, and in cancer, such as invasion and dissemination. Here, we describe a collection of protocols for 3D culture of mammary organoids in different ECMs and for immunofluorescence staining of 3D culture samples and mammary gland tissue sections. We illustrate expected phenotypic outcomes of each assay and provide troubleshooting tips for commonly encountered technical problems.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Biological Assay
  • Cell Culture Techniques / methods*
  • Cell Separation
  • Cell Shape / drug effects
  • Collagen / pharmacology
  • Collagen Type I / pharmacology
  • Drug Combinations
  • Epithelial Cells / cytology*
  • Epithelial Cells / drug effects
  • Female
  • Fluorescent Antibody Technique
  • Laminin / pharmacology
  • Mammary Glands, Animal / cytology
  • Mammary Glands, Animal / drug effects
  • Mammary Glands, Animal / growth & development*
  • Mice
  • Morphogenesis* / drug effects
  • Organoids / cytology
  • Organoids / drug effects
  • Phenotype
  • Proteoglycans / pharmacology
  • Rats
  • Serum Albumin, Bovine / metabolism
  • Staining and Labeling

Substances

  • Collagen Type I
  • Drug Combinations
  • Laminin
  • Proteoglycans
  • matrigel
  • Serum Albumin, Bovine
  • Collagen