GC-1 mRHBDD1 knockdown spermatogonia cells lose their spermatogenic capacity in mouse seminiferous tubules

BMC Cell Biology

Volumn 10, Issue , 2009, Pages

  Wang, Yong ^a   Song, Wei ^b   Li, Shuchun ^a   Guan, Xin ^a   Miao, Shiying ^a   Zong, Shudong ^b   Koide, S S ^c   Wang, Linfang ^a  

^a TSINGHUA UNIVERSITY   (China)

^b NATIONAL RESEARCH INSTITUTE FOR FAMILY PLANNING   (China)

^c POPULATION COUNCIL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; PROTEIN RHBDD1; UNCLASSIFIED DRUG; BORONIC ACID DERIVATIVE; BORTEZOMIB; EPIDERMAL GROWTH FACTOR RECEPTOR; GREEN FLUORESCENT PROTEIN; HYBRID PROTEIN; PYRAZINE DERIVATIVE; RHBDF1 PROTEIN, MOUSE; SMALL INTERFERING RNA;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL DIFFERENTIATION; CELL LOSS; CELL PROLIFERATION; CELL SURVIVAL; CONTROLLED STUDY; GENE EXPRESSION; GENE FUNCTION; IN VITRO STUDY; MALE; MOUSE; NONHUMAN; REGULATORY MECHANISM; SEMINIFEROUS TUBULE; SPERMATOGENESIS; SPERMATOGONIUM; ULTRAVIOLET IRRADIATION; ANIMAL; BAGG ALBINO MOUSE; CELL LINE; CYTOLOGY; DRUG EFFECT; FLOW CYTOMETRY; GENE EXPRESSION PROFILING; GENE SILENCING; GENETIC TRANSFECTION; GENETICS; METABOLISM; PHYSIOLOGY; RADIATION EXPOSURE; REGENERATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TESTIS; TRANSPLANTATION; ULTRAVIOLET RADIATION; WESTERN BLOTTING;

MAMMALIA; RATTUS;

ANIMALS; APOPTOSIS; BLOTTING, WESTERN; BORONIC ACIDS; CELL LINE; CELL PROLIFERATION; FLOW CYTOMETRY; GENE EXPRESSION PROFILING; GENE KNOCKDOWN TECHNIQUES; GREEN FLUORESCENT PROTEINS; MALE; MICE; MICE, INBRED BALB C; PYRAZINES; RECEPTOR, EPIDERMAL GROWTH FACTOR; RECOMBINANT FUSION PROTEINS; REGENERATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, SMALL INTERFERING; SEMINIFEROUS TUBULES; SPERMATOGENESIS; SPERMATOGONIA; TESTIS; TRANSFECTION; ULTRAVIOLET RAYS;

EID: 65649126814     PISSN: None     EISSN: 14712121     Source Type: Journal    
DOI: 10.1186/1471-2121-10-25     Document Type: Article

References (22)

1. Wang RA Nakane PK Koji T Autonomous cell death of mouse male germ cells during fetal and postnatal period Biol Reprod 1998, 58(5):1250-1256 10.1095/biolreprod58.5.1250 9603260
2. Rodriguez I Ody C Araki K Garcia I Vassalli P An early and massive wave of germinal cell apoptosis is required for the development of functional spermatogenesis Embo J 1997, 16(9):2262-2270 1169828 9171341 10.1093/ emboj/16.9.2262
3. Mori C Nakamura N Dix DJ Fujioka M Nakagawa S Shiota K Eddy EM Morphological analysis of germ cell apoptosis during postnatal testis development in normal and Hsp 70-2 knockout mice Dev Dyn 1997, 208(1):125-136 10.1002/ (SICI)1097-0177(199701)208:1<125::AID-AJA12>3.0.CO;2-5 8989527
4. Billig H Furuta I Rivier C Tapanainen J Parvinen M Hsueh AJ Apoptosis in testis germ cells: Developmental changes in gonadotropin dependence and localization to selective tubule stages Endocrinology 1995, 136(1):5-12 10.1210/en.136.1.5 7828558
5. Bartke A Apoptosis of male germ cells, a generalized or a cell type-specific phenomenon? Endocrinology 1995, 136(1):3-4 10.1210/ en.136.1.3 7828545
6. Print CG Loveland KL Germ cell suicide: New insights into apoptosis during spermatogenesis Bioessays 2000, 22(5):423-430 10.1002/ (SICI)1521-1878(200005)22:5<423::AID-BIES4>3.0.CO;2-0 10797482
7. Schaller CE Wang CL Beck-Engeser G Goss L Scott HS Anderson MS Wabl M Expression of Aire and the early wave of apoptosis in spermatogenesis J Immunol 2008, 180(3):1338-1343 18209027
8. Koonin EV Makarova KS Rogozin IB Davidovic L Letellier MC Pellegrini L The rhomboids: A nearly ubiquitous family of intramembrane serine proteases that probably evolved by multiple ancient horizontal gene transfers Genome Biol 2003, 4(3):R19 153459 12620104 10.1186/ gb-2003-4-3-r19
9. Lee JR Urban S Garvey CF Freeman M Regulated intracellular ligand transport and proteolysis control EGF signal activation in Drosophila Cell 2001, 107(2):161-171 10.1016/S0092-8674(01)00526-8 11672524
10. Urban S Lee JR Freeman M Drosophila rhomboid-1 defines a family of putative intramembrane serine proteases Cell 2001, 107(2)173-182 10.1016/ S0092-8674(01)00525-6 11672525
11. McQuibban GA Saurya S Freeman M Mitochondrial membrane remodelling regulated by a conserved rhomboid protease Nature 2003, 423(6939):537-541 10.1038/nature01633 12774122
12. Howell SA Hackett F Jongco AM Withers-Martinez C Kim K Carruthers VB Blackman MJ Distinct mechanisms govern proteolytic shedding of a key invasion protein in apicomplexan pathogens Mol Microbiol 2005, 57(5):1342-1356 10.1111/j.1365-2958.2005.04772.x 16102004
13. Wang Y Guan X Fok KL Li S Zhang X Miao S Zong S Koide SS Chan HC Wang L A novel member of the Rhomboid family, RHBDD1, regulates BIK-mediated apoptosis Cell Mol Life Sci 2008, 65(23):3822-3829 10.1007/ s00018-008-8452-0 18953687
14. Urban S Rhomboid proteins: Conserved membrane proteases with divergent biological functions Genes Dev 2006, 20(22):3054-3068 10.1101/ gad.1488606 17114579
15. Pascall JC Brown KD Intramembrane cleavage of ephrinB3 by the human rhomboid family protease, RHBDL2 Biochem Biophys Res Commun 2004, 317(1):244-252 10.1016/j.bbrc.2004.03.039 15047175
16. Lohi O Urban S Freeman M Diverse substrate recognition mechanisms for rhomboids; thrombomodulin is cleaved by Mammalian rhomboids Curr Biol 2004, 14(3):236-241 14761657
17. Gottlieb E OPA1 and PARL keep a lid on apoptosis Cell 2006, 126(1):27-29 10.1016/j.cell.2006.06.030 16839872
18. Cipolat S Rudka T Hartmann D Costa V Serneels L Craessaerts K Metzger K Frezza C Annaert W D'Adamio L et al Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling Cell 2006, 126(1):163-175 10.1016/j.cell.2006.06.021 16839884
19. McQuibban GA Lee JR Zheng L Juusola M Freeman M Normal mitochondrial dynamics requires rhomboid-7 and affects Drosophila lifespan and neuronal function Curr Biol 2006, 16(10):982-989 10.1016/ j.cub.2006.03.062 16713954
20. Allan DJHB Kerr JFR Cell death in spermatogenesis London: Oxford university Press 1987
21. Allan DJ Harmon BV Roberts SA Spermatogonial apoptosis has three morphologically recognizable phases and shows no circadian rhythm during normal spermatogenesis in the rat Cell Prolif 1992, 25(3):241-250 10.1111/j.1365-2184.1992.tb01399.x 1596537
22. Brinster RL Germline stem cell transplantation and transgenesis Science 2002, 296(5576):2174-2176 10.1126/science.1071607 12077400