JoVE Biology

Mouse Mammary Epithelial Cells form Mammospheres During Lactogenic Differentiation

1, 1

1Department of Pathology, F. Edward Hebert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD

    Downloads Comments Metrics

    You must be subscribed to JoVE to access this content.

    Enter your email to receive a free trial:


    Enter your email below to get your free 10 minute trial to JoVE!

    Admit it, you like to watch.



    HC11 lactogenic differentiation can be characterized by the formation of domed structures referred to as mammospheres. The structures can be enumerated by phase contrast microscopy to aid in quantifying lactogenic differentiation.

    Date Published: 10/06/2009, Issue 32; doi: 10.3791/1265

    Cite this Article

    Morrison, B., Cutler, M. L. Mouse Mammary Epithelial Cells form Mammospheres During Lactogenic Differentiation. J. Vis. Exp. (32), e1265, doi:10.3791/1265 (2009).


    A phenotypic measure commonly used to determine the degree of lactogenic differentiation in mouse mammary epithelial cell cultures is the formation of dome shaped cell structures referred to as mammospheres 1. The HC11 cell line has been employed as a model system for the study of regulation of mammary lactogenic differentiation both in vitro and in vivo 2. The HC11 cells differentiate and synthesize milk proteins in response to treatment with lactogenic hormones. Following the growth of HC11 mouse mammary epithelial cells to confluence, lactogenic differentiation was induced by the addition of a combination of lactogenic hormones including dexamethasone, insulin, and prolactin, referred to as DIP. The HC11 cells induced to differentiate were photographed at times up to 120 hours post induction of differentiation and the number of mammospheres that appeared in each culture was enumerated. The size of the individual mammospheres correlates with the degree of differentiation and this is depicted in the images of the differentiating cells.


    1. The HC11 cells were grown to confluence for 6 days in RPMI 1640 medium supplemented with 10% fetal calf serum, 5μg/ml Insulin, 10 mM HEPES, 10ng/ml epidermal growth factor (EGF) to establish competence.
    2. The cells were washed with PBS and maintained in growth media without EGF for 24 hours.
    3. To induce lactogenic differentiation the cells were incubated in differentiation media, i.e. RPMI with dexamethasone (10-6 M), insulin (5 μg /ml) and prolactin (5 μg /ml) referred to as DIP.
    4. At the stated times post-DIP addition, mammospheres were photographed and enumerated by phase contrast microscopy using an Olympus IX71 microscope with digital camera.

    Representative Results:

    Low power magnification of normal mammary epithelial cell monolayers and multiple mammospheres, as well as high power magnification of a single mammosphere are shown in Figure 1, respectively.

    Figure 1. Mammospheres. (a) Normal mammary epithelial cell monolayers should be displayed as a flat layer of confluent cells. (b) After 3-5 days of DIP stimulation multiple mammospheres appear.  Photograph taken 5 days post DIP addition. (c) Higher magnification of a single field containing mammospheres at 5 days post DIP addition.

    Subscription Required. Please recommend JoVE to your librarian.


    In order for this technique to be successful and of the best quality, the epithelial cells must be maintained at confluence prior to being induced with lactogenic hormones. There may be situations where there are numerous mammospheres, which makes the quantification difficult. Thus, for quantitative purposes it is best to photograph the mammospheres at a time point when the number of mammospheres is able to be counted.

    While there are various molecular markers used to determine the degree of lactogenic differentiation of mammary epithelial cells, there are few morphological markers used for cells grown in 2D culture. The ability of epithelial cell monolayers to form miniature dome structures where milk proteins can accumulate provides a mode by which the morphological changes that occur during this developmental process can be monitored.

    Subscription Required. Please recommend JoVE to your librarian.



    Funds from Congressionally Directed Medical Research Fund grant (DAMD17-01-0264) to M.L. Cutler and United States Military Cancer Institute to M.L. Cutler supported the work.


    Name Company Catalog Number Comments
    RPMI Invitrogen 21870076
    Fetal Bovine Serum Atlanta Biologicals S11550
    L-Glutamine GIBCO, by Life Technologies 25030
    PenStrep GIBCO, by Life Technologies 15140
    Hepes Quality Biological, Inc. 118089060
    EGF Sigma-Aldrich E9644
    Insulin GIBCO, by Life Technologies 12585-014
    Dexamethasone Sigma-Aldrich D1756
    Microscope Olympus Corporation IX71
    Digital Camera QImaging Retiga 2000RV Fast 1394


    1. Blatchford, D. R., Hendry, K. A., Turner, M. D., Burgoyne, R. D., Wilde, C. J. Vectorial secretion by constitutive and regulated secretory pathways in mammary epithelial cells. Epithelial Cell Biol. 4, 8-16 (1995).
    2. Wang, W. Glucocorticoid induced expression of connective tissue growth factor contributes to lactogenic differentiation of mouse mammary epithelial cells. J Cell Physiol. 214, 38-46 (2008).



    Very nice job and well done video

    Posted by: Silvio M.December 9, 2009, 12:54 AM

    interesting work and very nice video presentation.

    Do you really culture the cells during the differenciation step without serum.

    Many thanks for your time.

    Posted by: AnonymousApril 30, 2010, 10:25 AM

    Hi, I can't down load the pdf , why?

    Posted by: AnonymousSeptember 23, 2011, 4:51 AM

    Post a Question / Comment / Request

    You must be signed in to post a comment. Please or create an account.


    simple hit counter