QUICK SEARCH:   [advanced] Author: Keyword(s):
Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents

doi: 10.1242/10.1242/jcs.00503

This Article Summary Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Related articles in JCS Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Schmeichel, K. L. Articles by Bissell, M. J. Search for Related Content PubMed PubMed Citation Articles by Schmeichel, K. L. Articles by Bissell, M. J.

Modeling tissue-specific signaling and organ function in three dimensions

Lawrence Berkeley National Laboratory, 1 Cyclotron Road, MS 83-101, Berkeley, CA 94720, USA

View larger version (41K): [in a new window]   Fig. 1. Hierarchical modeling of human breast function. Similarities between the organization of human and mouse mammary glands have enabled observations in one tissue to be transferred to the other. This dynamic exchange of information has led to the gradual development of mammary gland models that now represent a continuum of organotypic systems ranging in complexity from monotypic 3D cultures to multicellular co-cultures to in vivo xenograft models. Each of the 3D models depicted here represents a physiologically relevant assay in its own right. However, when engineered with common cellular components and used in series, these models become invaluable tools for the identification and verification of disease-related molecules as well as for the design and translation of effective drug therapies. Future in vivo models that are more faithful to the human mammary microenvironment may be achieved in a `humanized' mouse model in which mammary glands are entirely repopulated by breast cell types of human origin. Ep, epithelial cell; Myoep, myoepithelial cell. Adapted from previous publications (Ronnov-Jessen et al., 1996; Schmeichel et al., 1998).

View larger version (50K): [in a new window]   Fig. 2. Signaling mechanisms studied in monotypic 3D cultures of human mammary epithelial cell lines. The phenotypes of human mammary epithelial cells can be readily distinguished in the context of 3D lrBM assays. After 10 days in culture, non-malignant cells form growth-arrested, polarized acini with central lumens, whereas malignant cells form apolar colonies of continually growing cells that vary in size and shape depending on the degree of tumorigenicity. A number of studies, some of which are depicted here, have utilized this assay to explore the molecular regulation of normal breast (e.g., lumen formation) as well as aberrant signaling during tumor progression and/or reversion. Individual studies are referenced in the text.

View larger version (27K): [in a new window]   Fig. 3. Using genetically engineered fibroblasts to elucidate stromal-epithelial interactions in organotypic skin co-cultures. Primary human keratinocytes maintain their stratified and differentiated morphology in 3D organotypic co-cultures regardless of whether dermal fibroblasts included are of human (HDF, A) or mouse (MEF, mouse embryonic fibroblasts, B) origin. Substitution of wild-type mouse fibroblasts with genetically engineered fibroblasts from transgenic animals allows for a detailed analysis of the molecular underpinnings of epithelial stromal interactions. Here, c-jun-/- (C) and junB-/- (D) fibroblasts are shown to have hypo- or hyperproliferative effects, respectively, on the morphology of human skin. This study demonstrates the utility of 3D co-culture methodologies in dissecting the molecular determinants of paracrine signaling networks. This figure is summarized from a previously published figure (Szabowski et al., 2000).

View larger version (37K): [in a new window]   Fig. 4. Modeling mammary acinar structure in 3D organotypic co-cultures. Purified primary human luminal epithelial cells were embedded and cultured in lrBM (A) or collagen I gels (B,C) in the absence (A,B) or presence (C) of purified myoepithelial cells (MEP). Cultures were double stained for the lumenal marker, sialomucin (red) and the basolateral marker, epithelial-specific antigen (ESA; green). Luminal epithelial cells form polarized organotypic spheres in lrBM but adopt inverse polarity in collagen I gels. Addition of purified myoepithelial cells to luminal epithelial cells in collagen I corrects acinar polarity (C) and results in formation of a bilayered organotypic structure. Reproduced with permission from Gudjonsson et al. (Gudjonsson et al., 2002a).