Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Sep;13(5):774-6.
doi: 10.1038/aja.2011.6. Epub 2011 Apr 11.

High-magnification observation of seminiferous tubules through the tunica albuginea by two-photon laser scanning microscopy

Affiliations

High-magnification observation of seminiferous tubules through the tunica albuginea by two-photon laser scanning microscopy

Vincent Achard et al. Asian J Androl. 2011 Sep.

Abstract

Testicular sperm extraction is widely used in the treatment of male infertility in cases of non-obstructive azoospermia. Identifying spermatogenetic foci within the testes is critical for testicular sperm extraction. Two-photon laser scanning microscopy (TPLSM) is an autofluorescence-based microscopy technique that allows observation at a cellular level in the depth of fresh living tissues and does not require any histological processing (fixation or staining). The wavelengths previously used have shown no phototoxicity on sperm. We used TPLSM to detect spermatogenetic foci in fresh mouse testicular parenchyma without disrupting the tunica albuginea. Fresh surgically retrieved testes were observed using TPLSM within 1 h after extraction. Contralateral testes for each animal were observed using standard histology. Using TPLSM we were able to observe and measure the diameter of seminiferous tubules through the tunica albuginea, similar to the histological control. Structures within epithelial tubules were also observed, although their nature has yet to be identified. TPLSM is a real-time microscopy technique that could detect spermatogenetic foci.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Photomicrographs of both testes obtained from the same animal. (a, b) Images obtained by live two-photon confocal scanning microscopy on a fresh whole testis through the TA without tissue preparation or staining, 1 h after extraction. (c, d) Images obtained from histological fields observed after classical histological processing of the other testis (fixation, paraffin embedding and trichrome counterstaining) and observation with a regular microscope. Lengths are given in micrometers (µm). ST, seminiferous tubules; TA, tunica albuginea.

References

    1. Ramasamy R, Lin K, Gosden LV, Rosenwaks Z, Palermo GD, et al. High serum FSH levels in men with nonobstructive azoospermia does not affect success of microdissection testicular sperm extraction. Fertil Steril. 2009;92:590–3. - PubMed
    1. Ramasamy R, Yagan N, Schlegel PN. Structural and functional changes to the testis after conventional versus microdissection testicular sperm extraction. Urology. 2005;65:1190–4. - PubMed
    1. Svoboda K, Yasuda R. Principles of two-photon excitation microscopy and its applications to neuroscience. Neuron. 2006;50:823–39. - PubMed
    1. Zipfel WR, Williams RM, Christie R, Nikitin AY, Hyman BT, et al. Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation. Proc Natl Acad Sci USA. 2003;100:7075–80. - PMC - PubMed
    1. Cahalan MD, Parker I, Wei SH, Miller MJ. Two-photon tissue imaging: seeing the immune system in a fresh light. Nat Rev Immunol. 2002;2:872–80. - PMC - PubMed