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PMID: 12642486 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

A role for actin dynamics in individualization during spermatogenesis in Drosophila melanogaster.

Development (Cambridge, England) ·Vol. 130 ·No. 9 ·2003-05-00 ·Pages 1805-16

Noguchi T, Miller KG

Abstract

In order to better understand the mechanism of sperm individualization during spermatogenesis in Drosophila melanogaster, we have developed an in vitro culture system in which we can perform live observation of individualization in isolated cysts. The whole process of individualization, during which a bundle of 64 syncytial spermatids is separated into individual sperm, takes place in these cultures. Individualization complexes, which consist of 64 cones of actin that assemble around the sperm nuclei, move to the basal end of the tails, forming a characteristic "cystic bulge" that contains an accumulation of cytoplasm, syncytial membrane and vesicles. The cystic bulge is the site of membrane remodeling and its movement was used to follow the progress of individualization. The speed of cystic bulge movement is fairly constant along the length of the cyst. Actin drugs, but not microtubule drugs inhibit cystic bulge movement, suggesting that the movement requires proper actin dynamics but not microtubules. GFP-tagged actin was expressed in the cyst and fluorescence recovery after photobleaching was monitored using confocal microscopy to analyze actin dynamics in cones. Actin turns over throughout the cone, with that at the leading edge of the cones turning over with slightly faster kinetics. Actin does not treadmill from the front to the back of the cone. Actin in moving actin cones turns over in about 12 minutes, although prior to onset of movement, turnover is much slower. Visualization of membrane using FM1-43 reveals that the cystic bulge has an extremely complicated series of membrane invaginations and the transition from syncytial to individualized spermatids occurs at the front of the actin cones. We also suggest that endocytosis and exocytosis might not be important for membrane remodeling. This system should be suitable for analysis of defects in male sterile mutants and for investigating other steps of spermatogenesis.

MeSH Terms
Actins/metabolism Animals Cell Nucleus/metabolism Culture Techniques Drosophila melanogaster/physiology Male Microtubules/metabolism Spermatogenesis/physiology
Chemicals
Actins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Noguchi Tatsuhiko
Department of Biology, Washington University in St Louis, Campus Box 1229, 1 Brookings Drive, St Louis, MO 63130, USA. [email protected]
Miller Kathryn G
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2003-05-00
Pages
1805-16
Language
English
Region
England
NLM ID
8701744
Subset
IM
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