Stem cells in endometrium and their role in the pathogenesis of endometriosis

被引:131
作者
Marin Figueira, Paula Gabriela [2 ]
Abrao, Mauricio Simoes [2 ]
Krikun, Graciela [1 ]
Taylor, Hugh [1 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT 06510 USA
[2] Univ Sao Paulo, Dept Obstet & Gynecol, Sao Paulo, Brazil
来源
REPRODUCTIVE SCIENCE | 2011年 / 1221卷
关键词
endometrium; endometriosis; stem cells; ADULT HUMAN ENDOMETRIUM; SIDE-POPULATION; MENSTRUAL DISSEMINATION; EXPRESSION; DIFFERENTIATION; GENOMICS; MARKERS; TISSUE; BLOOD;
D O I
10.1111/j.1749-6632.2011.05969.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human endometrium is a dynamic tissue that undergoes cycles of growth and regression with each menstrual cycle. Adult progenitor stem cells are likely responsible for this remarkable regenerative capacity; these same progenitor stem cells may also have an enhanced capacity to generate endometriosis if shed in a retrograde fashion. The progenitor stem cells reside in the uterus; however, less-committed mesenchymal stem cells may also travel from other tissues such as bone marrow to repopulate the progenitor population. Mesenchymal stem cells are also involved in the pathogenesis of endometriosis and may be the principle source of endometriosis outside of the peritoneal cavity when they differentiate into endometriosis in ectopic locations. Finally, besides progenitor stem cells, recent publications have identified multipotent stem cells in the endometrium. These multipotent stem cells are a readily available source of cells that are useful in tissue engineering and regenerative medicine. Endometrial stem cells have been used to generate chondrocytes, myocytes, neurons, and adiposites in vitro as well as to replace dopaminergic neurons in a murine model of Parkinson's disease.
引用
收藏
页码:10 / 17
页数:8
相关论文
共 54 条
[1]   Cell differentiation - Hepatocytes from nonhepatic adult stem cells [J].
Alison, MR ;
Poulsom, R ;
Jeffery, R ;
Dhillon, AP ;
Quaglia, A ;
Jacob, J ;
Novelli, M ;
Prentice, G ;
Williamson, J ;
Wright, NA .
NATURE, 2000, 406 (6793) :257-257
[2]   Stem cells: the intestinal stem cell as a paradigm [J].
Bach, SP ;
Renehan, AG ;
Potten, CS .
CARCINOGENESIS, 2000, 21 (03) :469-476
[3]   OCT-4 expression in follicular and luteal phase endometrium: a pilot study [J].
Bentz, Eva-Katrin ;
Kenning, Marina ;
Schneeberger, Christian ;
Kolbus, Andrea ;
Huber, Johannes C. ;
Hefler, Lukas A. ;
Tempfer, Clemens B. .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2010, 8
[4]   History and perspective of stem cell research [J].
Bongso, A ;
Richards, M .
BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2004, 18 (06) :827-842
[5]   A side order of stem cells: The SP phenotype [J].
Challen, GA ;
Little, MH .
STEM CELLS, 2006, 24 (01) :3-12
[6]   Clonogenicity of human endometrial epithelial and stromal cellss [J].
Chan, RWS ;
Schwab, KE ;
Gargett, CE .
BIOLOGY OF REPRODUCTION, 2004, 70 (06) :1738-1750
[7]   Lifetime expression of stem cell markers in the uterine endometrium [J].
Cho, NH ;
Park, YK ;
Kim, YT ;
Yang, H ;
Kim, SK .
FERTILITY AND STERILITY, 2004, 81 (02) :403-407
[8]   Contribution of bone marrow-derived stem cells to endometrium and endometriosis [J].
Du, Hongling ;
Taylor, Hugh S. .
STEM CELLS, 2007, 25 (08) :2082-2086
[9]   Stem cells and reproduction [J].
Du, Hongling ;
Taylor, Hugh S. .
CURRENT OPINION IN OBSTETRICS & GYNECOLOGY, 2010, 22 (03) :235-241
[10]   Stem Cells and Female Reproduction [J].
Du, Hongling ;
Taylor, Hugh S. .
REPRODUCTIVE SCIENCES, 2009, 16 (02) :126-139