TY - JOUR
T1 - Common adult stem cells in the human breast give rise to glandular and myoepithelial cell lineages
T2 - A new cell biological concept
AU - Böcker, Werner
AU - Moll, Roland
AU - Poremba, Christopher
AU - Holland, Roland
AU - Van Diest, Paul J.
AU - Dervan, Peter
AU - Bürger, Horst
AU - Wai, Daniel
AU - Diallo, Raihanatou Ina
AU - Brandt, Burkhard
AU - Herbst, Hermann
AU - Schmidt, Ansgar
AU - Lerch, Markus M.
AU - Buchwallow, Igor B.
N1 - Funding Information:
This study was supported by Deutsche Krebshilfe; 10-1681-Bü-I. Address reprint requests to: Dr. Werner Boecker, Professor of Pathology, Gerhard Domagk-Institute of Pathology, Domagkstrasse 17, D-48149 Münster, Germany. E-mail: [email protected]
PY - 2002/6
Y1 - 2002/6
N2 - Breast biology and pathology are currently shaped by the two-cell concept that recognizes only glandular and myoepithelial cells. In the present study, we have visualized a previously unidentified cell population within the epithelial compartment of the breast, which displays the phenotypic characteristics of a committed stem cell. Immunofluorescence double labeling with digital image processing and Western blotting were applied to normal breast tissue as well as to noninvasive and invasive breast cancers using antibodies to basal cytokeratin 5 (Ck5), glandular cytokeratins 8/18 (Ck8/18/19), and smooth muscle α-actin (SMA) as markers for myoepithelial cells (SMA). A distinct population of cells was identified that expressed Ck5 in the absence of Ck8/18/19 or SMA. These cells differentiate toward glandular epithelial or myoepithelial Ck5-negative end cells passing through either Ck5/Ck8/18/19 or Ck5/SMA-positive intermediates. Our experiments clearly demonstrate a precursor or committed stem cell function of the Ck5-positive cell that is responsible for regeneration of the human adult breast epithelium. However, the observation that the vast majority of breast cancers display the glandular epithelial immunophenotype strongly suggests that the neoplastic cells derive from a late stage of the glandular epithelial differentiation pathway. The significance of this new cell biological model is that it might serve as a tool to unravel the regulatory mechanisms that govern regeneration and abnormal proliferation of breast epithelium at the cellular level.
AB - Breast biology and pathology are currently shaped by the two-cell concept that recognizes only glandular and myoepithelial cells. In the present study, we have visualized a previously unidentified cell population within the epithelial compartment of the breast, which displays the phenotypic characteristics of a committed stem cell. Immunofluorescence double labeling with digital image processing and Western blotting were applied to normal breast tissue as well as to noninvasive and invasive breast cancers using antibodies to basal cytokeratin 5 (Ck5), glandular cytokeratins 8/18 (Ck8/18/19), and smooth muscle α-actin (SMA) as markers for myoepithelial cells (SMA). A distinct population of cells was identified that expressed Ck5 in the absence of Ck8/18/19 or SMA. These cells differentiate toward glandular epithelial or myoepithelial Ck5-negative end cells passing through either Ck5/Ck8/18/19 or Ck5/SMA-positive intermediates. Our experiments clearly demonstrate a precursor or committed stem cell function of the Ck5-positive cell that is responsible for regeneration of the human adult breast epithelium. However, the observation that the vast majority of breast cancers display the glandular epithelial immunophenotype strongly suggests that the neoplastic cells derive from a late stage of the glandular epithelial differentiation pathway. The significance of this new cell biological model is that it might serve as a tool to unravel the regulatory mechanisms that govern regeneration and abnormal proliferation of breast epithelium at the cellular level.
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U2 - 10.1097/01.lab.0000017371.72714.c5
DO - 10.1097/01.lab.0000017371.72714.c5
M3 - Article
C2 - 12065684
AN - SCOPUS:0036278690
SN - 0023-6837
VL - 82
SP - 737
EP - 745
JO - Laboratory Investigation
JF - Laboratory Investigation
IS - 6
ER -