Skip to main content
. 2015 Jul 21;20(1-2):63–73. doi: 10.1007/s10911-015-9336-1

Table 1.

Expression of ER and PR in distinct normal human mammary epithelial subpopulations

Markers Phenotype Description ER expression PR expression Detection method
CD10
CD24
CD44 [33]
CD10 CD24 CD44+ Stem/Progenitor cells +/− Semi-quantitative RT-PCRa
EpCAM
CD49f
CD133
MUC1
CD10
THY1 [28]
EpCAM+ CD49f Mature Luminal Cells ++ ++ Long SAGEb and Affimetrix analysis, qRT-PCRc
MUC1+CD133+
CD10 THY1
EpCAM+ CD49f+ Bipotent progenitors + ++
MUC1 CD133
CD10+ THY1+
EpCAM+ CD49f+ Luminal-restricted progenitors +++ +
MUC1+ CD133+
CD10 THY1
CD31/CD45 (Lind)
EpCAM
CD49f
ALDH
ErbB3 [29]
Lin EpCAM+CD49f Mature Luminal cells +++ +++ qRT-PCR
Lin EpCAM+ CD49f+ ALDH+ ErbB3+ Luminal progenitors (High CFC frequency) ++ ++
Lin EpCAM+ CD49f+ ALDH - ErbB3+ Luminal progenitors (Low CFC frequency) ++ ++
CD31/CD45/CD235a
(Lin)
EpCAM
CD49f
[25, 26]
Lin EpCAM+ CD49f Mature Luminal cells +++ +++ qRT-PCR; ICCe (% of positive cells)
55 % 71 %
Lin EpCAM+ CD49f+ Luminal Progenitor Cells + +
28 % 2 %
Lin EpCAM CD49fHigh MaSC-enriched Basal cells +/− +
0.2 % 0.0 %
ALDH [27] ALDH+ Stem/progenitor cells 0 % NDf ICC; Flow cytometry (% of positive cells)

a RT-PCR reverse transcription polymerase chain reaction

b LongSAGE long serial analysis of gene expression

c qRT-PCR quantitative Real-Time PCR

d Lin lineage

e ICC immunocytochemistry

f ND not determined