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A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield

Testicular sperm extraction is a common procedure used to find spermatogenic cells in men with nonobstructive azoospermia. The laboratory processing of biopsied testicular tissues needs to be performed meticulously to acquire a high yield of cells. In this study, the effectiveness of mincing the tis...

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Autores principales: Ozkavukcu, Sinan, Ibis, Ebru, Kizil, Sule, Isbacar, Suheyla, Aydos, Kaan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236328/
https://www.ncbi.nlm.nih.gov/pubmed/25038178
http://dx.doi.org/10.4103/1008-682X.132468
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author Ozkavukcu, Sinan
Ibis, Ebru
Kizil, Sule
Isbacar, Suheyla
Aydos, Kaan
author_facet Ozkavukcu, Sinan
Ibis, Ebru
Kizil, Sule
Isbacar, Suheyla
Aydos, Kaan
author_sort Ozkavukcu, Sinan
collection PubMed
description Testicular sperm extraction is a common procedure used to find spermatogenic cells in men with nonobstructive azoospermia. The laboratory processing of biopsied testicular tissues needs to be performed meticulously to acquire a high yield of cells. In this study, the effectiveness of mincing the tissues after testicular biopsy was assessed using histological evaluation, as was the possible adverse effect of residual tissue on the migration of spermatogenic cells during density gradient centrifugation. Our results indicate that testicular residual tissue, when laid on the density gradient medium along with the sperm wash, hinders the spermatogenic cells’ forming a pellet during centrifugation, and therefore impairs the intracytoplasmic sperm injection procedure. Whereas the mean number of recovered cells from the sperm wash medium (SWM) with residual tissue is 39.435 ± 24.849, it was notably higher (60.189 ± 28.214 cells) in the SWM without minced tissues. The remaining tissue contained no functional seminiferous tubules or spermatogenic cells in histological sections. In conclusion, the remaining residual tissue after mincing biopsied testicular tissue does not add any functional or cellular contribution to spermatogenic cell retrieval; in fact, it may block the cellular elements in the accompanying cell suspension from migrating through the gradient layers to form a pellet during centrifugation and cause loss of spermatogenic cells.
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spelling pubmed-42363282014-11-25 A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield Ozkavukcu, Sinan Ibis, Ebru Kizil, Sule Isbacar, Suheyla Aydos, Kaan Asian J Androl Original Article Testicular sperm extraction is a common procedure used to find spermatogenic cells in men with nonobstructive azoospermia. The laboratory processing of biopsied testicular tissues needs to be performed meticulously to acquire a high yield of cells. In this study, the effectiveness of mincing the tissues after testicular biopsy was assessed using histological evaluation, as was the possible adverse effect of residual tissue on the migration of spermatogenic cells during density gradient centrifugation. Our results indicate that testicular residual tissue, when laid on the density gradient medium along with the sperm wash, hinders the spermatogenic cells’ forming a pellet during centrifugation, and therefore impairs the intracytoplasmic sperm injection procedure. Whereas the mean number of recovered cells from the sperm wash medium (SWM) with residual tissue is 39.435 ± 24.849, it was notably higher (60.189 ± 28.214 cells) in the SWM without minced tissues. The remaining tissue contained no functional seminiferous tubules or spermatogenic cells in histological sections. In conclusion, the remaining residual tissue after mincing biopsied testicular tissue does not add any functional or cellular contribution to spermatogenic cell retrieval; in fact, it may block the cellular elements in the accompanying cell suspension from migrating through the gradient layers to form a pellet during centrifugation and cause loss of spermatogenic cells. Medknow Publications & Media Pvt Ltd 2014 2014-07-01 /pmc/articles/PMC4236328/ /pubmed/25038178 http://dx.doi.org/10.4103/1008-682X.132468 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ozkavukcu, Sinan
Ibis, Ebru
Kizil, Sule
Isbacar, Suheyla
Aydos, Kaan
A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title_full A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title_fullStr A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title_full_unstemmed A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title_short A laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
title_sort laboratory modification to testicular sperm preparation technique improves spermatogenic cell yield
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236328/
https://www.ncbi.nlm.nih.gov/pubmed/25038178
http://dx.doi.org/10.4103/1008-682X.132468
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