Literature DB >> 2806122

Functional differentiation and alveolar morphogenesis of primary mammary cultures on reconstituted basement membrane.

M H Barcellos-Hoff1, J Aggeler, T G Ram, M J Bissell.   

Abstract

An essential feature of mammary gland differentiation during pregnancy is the formation of alveoli composed of polarized epithelial cells, which, under the influence of lactogenic hormones, secrete vectorially and sequester milk proteins. Previous culture studies have described either organization of cells polarized towards lumina containing little or no demonstrable tissue-specific protein, or establishment of functional secretory cells exhibiting little or no glandular architecture. In this paper, we report that tissue-specific vectorial secretion coincides with the formation of functional alveoli-like structures by primary mammary epithelial cells cultured on a reconstituted basement membrane matrix (derived from Engelbreth-Holm-Swarm murine tumour). Morphogenesis of these unique three-dimensional structures was initiated by cell-directed remodelling of the exogenous matrix leading to reorganization of cells into matrix-ensheathed aggregates by 24 h after plating. The aggregates subsequently cavitated, so that by day 6 the cells were organized into hollow spheres in which apical cell surfaces faced lumina sealed by tight junctions and basal surfaces were surrounded by a distinct basal lamina. The profiles of proteins secreted into the apical (luminal) and basal (medium) compartments indicated that these alveoli-like structures were capable of an appreciable amount of vectorial secretion. Immunoprecipitation with a broad spectrum milk antiserum showed that more than 80% of caseins were secreted into the lumina, whereas iron-binding proteins (both lactoferrin and transferrin) were present in comparable amounts in each compartment. Thus, these mammary cells established protein targeting pathways directing milk-specific proteins to the luminal compartment. A time course monitoring secretory activity demonstrated that establishment of tissue-specific vectorial secretion and increased total and milk protein secretion coincided with functional alveolar-like multicellular architecture. This culture system is unique among models of epithelial cell polarity in that it demonstrates several aspects of epithelial cell polarization: vectorial secretion, apical junctions, a sequestered compartment and formation of a basal lamina. These lumina-containing structures therefore reproduce the dual role of mammary epithelia to secrete vectorially and to sequester milk proteins. Thus, in addition to maintaining tissue-specific cytodifferentiation and function, a basement membrane promotes the expression of tissue-like morphogenesis.

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Year:  1989        PMID: 2806122      PMCID: PMC2948482          DOI: 10.1242/dev.105.2.223

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  53 in total

1.  Regulation of gene expression in adult rat hepatocytes cultured on a basement membrane matrix.

Authors:  E G Schuetz; D Li; C J Omiecinski; U Muller-Eberhard; H K Kleinman; B Elswick; P S Guzelian
Journal:  J Cell Physiol       Date:  1988-03       Impact factor: 6.384

Review 2.  Integrins: a family of cell surface receptors.

Authors:  R O Hynes
Journal:  Cell       Date:  1987-02-27       Impact factor: 41.582

3.  Milk protein expression and ductal morphogenesis in the mammary gland in vitro: hormone-dependent and -independent phases of adipocyte-mammary epithelial cell interaction.

Authors:  D Wiens; C S Park; F E Stockdale
Journal:  Dev Biol       Date:  1987-03       Impact factor: 3.582

Review 4.  Constitutive and regulated secretion of proteins.

Authors:  T L Burgess; R B Kelly
Journal:  Annu Rev Cell Biol       Date:  1987

5.  Elvax 40P implants: sustained, local release of bioactive molecules influencing mammary ductal development.

Authors:  G B Silberstein; C W Daniel
Journal:  Dev Biol       Date:  1982-09       Impact factor: 3.582

6.  Collagen reduces glycosaminoglycan degradation by cultured mammary epithelial cells: possible mechanism for basal lamina formation.

Authors:  G David; M R Bernfield
Journal:  Proc Natl Acad Sci U S A       Date:  1979-02       Impact factor: 11.205

7.  Regulation of rat mammary gene expression by extracellular matrix components.

Authors:  J L Blum; M E Zeigler; M S Wicha
Journal:  Exp Cell Res       Date:  1987-12       Impact factor: 3.905

8.  Collagenous substrata regulate the nature and distribution of glycosaminoglycans produced by differentiated cultures of mouse mammary epithelial cells.

Authors:  G Parry; E Y Lee; D Farson; M Koval; M J Bissell
Journal:  Exp Cell Res       Date:  1985-02       Impact factor: 3.905

9.  Modulation of secreted proteins of mouse mammary epithelial cells by the collagenous substrata.

Authors:  E Y Lee; G Parry; M J Bissell
Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

10.  Effect of cell shape change on the function and differentiation of rabbit mammary cells in culture.

Authors:  M T Haeuptle; Y L Suard; E Bogenmann; H Reggio; L Racine; J P Kraehenbuhl
Journal:  J Cell Biol       Date:  1983-05       Impact factor: 10.539

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  280 in total

1.  Division of labor among the alpha6beta4 integrin, beta1 integrins, and an E3 laminin receptor to signal morphogenesis and beta-casein expression in mammary epithelial cells.

Authors:  J Muschler; A Lochter; C D Roskelley; P Yurchenco; M J Bissell
Journal:  Mol Biol Cell       Date:  1999-09       Impact factor: 4.138

2.  Behavior of a cell line derived from normal human hepatocytes on non-physiological and physiological-type substrates: evidence for enhancement of secretion of liver-specific proteins by a three-dimensional growth pattern.

Authors:  M Smalley; K Leiper; D Floyd; M Mobberley; T Ryder; C Selden; E A Roberts; H Hodgson
Journal:  In Vitro Cell Dev Biol Anim       Date:  1999-01       Impact factor: 2.416

Review 3.  Roles of hepatocyte growth factor/scatter factor and transforming growth factor-beta1 in mammary gland ductal morphogenesis.

Authors:  J V Soriano; M S Pepper; L Orci; R Montesano
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-04       Impact factor: 2.673

Review 4.  Control of normal mammary epithelial phenotype by integrins.

Authors:  C H Streuli; G M Edwards
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-04       Impact factor: 2.673

Review 5.  The potential influence of radiation-induced microenvironments in neoplastic progression.

Authors:  M H Barcellos-Hoff
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-04       Impact factor: 2.673

Review 6.  Structural cues from the tissue microenvironment are essential determinants of the human mammary epithelial cell phenotype.

Authors:  K L Schmeichel; V M Weaver; M J Bissell
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-04       Impact factor: 2.673

7.  Interactions between normal mammary epithelial cells and mammary tumour cells in a model system.

Authors:  L H Quarrie; J D Pitts; M E Finbow
Journal:  Cell Prolif       Date:  1999-12       Impact factor: 6.831

Review 8.  An atlas of mouse mammary gland development.

Authors:  M M Richert; K L Schwertfeger; J W Ryder; S M Anderson
Journal:  J Mammary Gland Biol Neoplasia       Date:  2000-04       Impact factor: 2.673

Review 9.  Feedback control of milk secretion from milk.

Authors:  M Peaker; C J Wilde
Journal:  J Mammary Gland Biol Neoplasia       Date:  1996-07       Impact factor: 2.673

Review 10.  Three-dimensional mammary primary culture model systems.

Authors:  M M Ip; K M Darcy
Journal:  J Mammary Gland Biol Neoplasia       Date:  1996-01       Impact factor: 2.673

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