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Expression patterns of cell-surface molecules on male germ line stem cells during postnatal mouse development
Kevin T Ebata1, Xiangfan Zhang, Makoto C Nagano
1Department of Obstetrics and Gynecology, Royal Victoria Hospital, McGill University, 687 Pine Avenue West, Montreal, Quebec, Canada H3A 1A1.
Molecular Reproduction and Development
|July 13, 2005
Summary
Mouse spermatogonial stem cells (SSCs) change cell-surface molecule expression with age. GFRalpha1 expression on SSCs is higher in pups than adults, impacting stem cell activity.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Stem Cell Research
Background:
- Spermatogonial stem cells (SSCs) are crucial for male fertility.
- SSC proliferation and activity differ significantly between neonatal, pup, and adult mice.
- Age-dependent changes in SSC characteristics are suspected but not fully understood.
Purpose of the Study:
- To investigate age-dependent differences in cell-surface molecule expression on mouse SSCs.
- To evaluate the role of GDNF receptor (GFRalpha1) in age-related SSC activity.
- To assess the in vitro response of SSCs to GDNF across different ages.
Main Methods:
- Immunomagnetic cell sorting was used to isolate SSCs based on markers like alpha(6) integrin, alpha(v) integrin, c-kit, and GFRalpha1.
- Spermatogonial transplantation assays were performed to determine stem cell activity.
- In vitro culture with GDNF was used to assess age-dependent responses.
Main Results:
- SSCs consistently expressed alpha(6) integrin but not alpha(v) integrin or c-kit, irrespective of age.
- GFRalpha1 expression on SSCs was higher in pups compared to neonatal and adult mice, correlating with higher stem cell activity.
- No age-dependent difference in SSC response to GDNF was observed in vitro, and GDNF receptor signaling subunits were not readily detected on SSCs.
Conclusions:
- Mouse SSCs exhibit age-dependent changes in cell-surface molecule expression, particularly GFRalpha1.
- GFRalpha1 expression levels correlate with SSC activity during postnatal development.
- GDNF receptor signaling may not be a primary driver of age-dependent SSC characteristics in vivo.