Sca-1 Expression Identifies Stem Cells in the Proximal Region of Prostatic Ducts with High Capacity to Reconstitute Prostatic Tissue
We previously showed that prostatic stem cells are concentrated in the proximal regions of prostatic ducts. We now report that these stem cells can be purified from isolated proximal duct regions by virtue of their high expression of the cell surface protein stem cell antigen 1 (Sca-1). In an in viv...
Saved in:
Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 102; no. 20; pp. 7180 - 7185 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
17.05.2005
National Acad Sciences |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | We previously showed that prostatic stem cells are concentrated in the proximal regions of prostatic ducts. We now report that these stem cells can be purified from isolated proximal duct regions by virtue of their high expression of the cell surface protein stem cell antigen 1 (Sca-1). In an in vivo prostate reconstitution assay, the purified Sca-1-expressing cell population isolated from the proximal region of ducts was more effective in generating prostatic tissue than a comparable population of Sca-1-depleted cells (203.0 ± 83.1 mg vs. 11.9 ± 9.2 mg) or a population of Sca-1-expressing cells isolated from the remaining regions of ducts (transit-amplifying cells) (31.9 ± 24.1 mg). Almost all of the proliferative capacity of the proximal duct Sca-1-expressing cell population resides within the fraction of cells that express high levels of Sca-1 (top one-third), with the proximal region of prostatic ducts containing 7.2-fold more Sca-1highcells than the remaining regions. More than 60% of the high-expressing cells coexpress α6 integrin and the antiapoptotic factor Bcl-2, markers that are also characteristic of stem cells of other origins. Further stratification of the phenotype of the stem cells may enable the development of rational therapies for treating prostate cancer and benign prostatic hyperplasia. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 To whom correspondence should be addressed. E-mail: pburger@uctgsh1.uct.ac.za. P.E.B., X.X., and S.C. contributed equally to this work. Communicated by David D. Sabatini, New York University School of Medicine, New York, NY, April 6, 2005 Author contributions: P.E.B., D.M., and E.L.W. designed research; P.E.B., X.X., S.C., S.N.S., K.G., and E.L.W. performed research; P.E.B., D.M., and E.L.W. analyzed data; and P.E.B. and E.L.W. wrote the paper. Abbreviations: MFI, mean fluorescence intensity; PE, phycoerythrin; Sca-1, stem cell antigen 1; UGM, urogenital sinus mesenchyme. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.0502761102 |