File:Human spermatozoa acrosomal protein SP-10.jpg
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Human Spermatozoa Acrosomal Protein SP-10
Immunofluorescent/differential interference contrast (DIC) micrographs (A–H) and diagrammatic representations (a–h; modified from Holstein and Roosen-Runge, 1981) of enzyme-dissociated human testicular cells stained with 4′6-diamidino-2-phenylindole (DAPl) II for DNA (blue), fluorescein isothiocyanate (FITC) for the acrosomal protein SP-10 (green) and tetramethylrhodamine B isothiocyanate (TRITC) for the SPANXa/d protein (red).
(A) This early round spermatid demonstrates a small acrosomal vesicle (overlying the nucleus) stained with the acrosomal marker SP-10 (green). SPANXa/d staining is associated with the nuclear periphery.
(B) Early cap-phase spermatid showing SPANXa/d staining of the nuclear periphery posterior to the early acrosomal cap. As the acrosomal cap migrates posteriorly and the spermatid begins to elongate
(C–F), SPANXa/d staining is associated with the nuclear envelope posterior to the acrosomal cap.
In D and E, it is evident that a SPANXa/d-negative region intervenes between the equatorial bulbs on either side of the acrosome and the SPANXa/d-positive nuclear envelope. In elongated spermatids
(G) and testicular spermatozoa (H), SPANXa/d staining is seen in the posterior head and cytoplasmic droplet. Occasional nuclear vacuoles demonstrating SPANXa/d staining are observed (B and C, arrows).
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Legend
- Blue, DNA
- red, acrosomal protein SP-10
- green, SPANXa/d.
- A, acrosome
- An, annulus
- C, centriole
- Fs, flagellum
- M, mitochondria
- Mt, manchette
- N, nucleus
- Sb, spindle-shaped body
Original file name: Figure 6. http://molehr.oxfordjournals.org/content/12/11/703/F6.expansion.html
Reference
<pubmed>17012309</pubmed>| Mol Hum Reprod.
© The Author 2006. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org
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