Spermatogenesis is a complex cellular process that is initiated with mitotic divisions of type A spermatogonial stem cells. The long-term objective of this application is to understand better the regulation of these initial steps of spermatogenesis, namely spermatogonial renewal, differentiation, or death. The applicant has succeeded in the isolation of highly pure populations of rat type A spermatogonia and demonstrated that these cell express the c-kit receptor. Stem cell factor (SCF) also phosphorylates this receptor in type A spermatogonia. Using this finding as a baseboard, the applicant now describes three Specific Aims to further the study of the spermatogonial life cycle.
Specific Aim A will examine the effect of SCF, alone and in combination with leukemia inhibiting factor and bFGF, on spermatogonial survival, renewal and differentiation in vitro. Both the soluble and membrane bound forms of SCF will be studied.
Specific Aim B will investigate the mechanisms of action of SCF in the spermatogonial population. Here, the principal objective is to characterize the signal transduction pathway(s) in type A cells which is activated by SCF. Also, the pathway(s) will be associated with spermatogonial survival, renewal and/or differentiation. Finally, Specific Aim C will test the hypothesis that telomerase is limited to spermatogonia and that the loss of this key enzyme is associated with the transition into meiosis. The applicant stresses the potential significance of work on isolated spermatogonia as it may relate to future studies for the transplant of stem cells to repopulate damaged or inoperative testes.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD033728-03
Application #
2889222
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Tasca, Richard J
Project Start
1997-04-01
Project End
2001-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Georgetown University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
He, Zuping; Jiang, Jiji; Kokkinaki, Maria et al. (2013) MiRNA-20 and mirna-106a regulate spermatogonial stem cell renewal at the post-transcriptional level via targeting STAT3 and Ccnd1. Stem Cells 31:2205-17
Dwyer, Andrew A; Sykiotis, Gerasimos P; Hayes, Frances J et al. (2013) Trial of recombinant follicle-stimulating hormone pretreatment for GnRH-induced fertility in patients with congenital hypogonadotropic hypogonadism. J Clin Endocrinol Metab 98:E1790-5
Kokkinaki, Maria; Lee, Tin-Lap; He, Zuping et al. (2010) Age affects gene expression in mouse spermatogonial stem/progenitor cells. Reproduction 139:1011-20
He, Zuping; Kokkinaki, Maria; Jiang, Jiji et al. (2010) Isolation, characterization, and culture of human spermatogonia. Biol Reprod 82:363-72
Balasinor, Nafisa H; D'Souza, Ryan; Nanaware, Padma et al. (2010) Effect of high intratesticular estrogen on global gene expression and testicular cell number in rats. Reprod Biol Endocrinol 8:72
Kokkinaki, Maria; Lee, Tin-Lap; He, Zuping et al. (2009) The molecular signature of spermatogonial stem/progenitor cells in the 6-day-old mouse testis. Biol Reprod 80:707-17
He, Zuping; Jiang, Jiji; Kokkinaki, Maria et al. (2009) Nodal signaling via an autocrine pathway promotes proliferation of mouse spermatogonial stem/progenitor cells through Smad2/3 and Oct-4 activation. Stem Cells 27:2580-90
Golestaneh, Nady; Kokkinaki, Maria; Pant, Disha et al. (2009) Pluripotent stem cells derived from adult human testes. Stem Cells Dev 18:1115-26
He, Zuping; Kokkinaki, Maria; Dym, Martin (2009) Signaling molecules and pathways regulating the fate of spermatogonial stem cells. Microsc Res Tech 72:586-95
He, Zuping; Kokkinaki, Maria; Pant, Disha et al. (2009) Small RNA molecules in the regulation of spermatogenesis. Reproduction 137:901-11

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