Whole-mount immunohistochemistry to study spermatogonial stem cells and spermatogenic lineage development in mice, monkeys, and humans.
Identifieur interne : 000798 ( Main/Exploration ); précédent : 000797; suivant : 000799Whole-mount immunohistochemistry to study spermatogonial stem cells and spermatogenic lineage development in mice, monkeys, and humans.
Auteurs : Kathrin Gassei [États-Unis] ; Hanna Valli ; Kyle E. OrwigSource :
- Methods in molecular biology (Clifton, N.J.) [ 1940-6029 ] ; 2014.
Descripteurs français
- KwdFr :
- Animaux, Canalicules séminifères (cytologie), Canalicules séminifères (métabolisme), Cellules souches (cytologie), Cellules souches (métabolisme), Différenciation cellulaire, Haplorhini, Humains, Immunohistochimie (), Lignage cellulaire, Mâle, Souris, Spermatogenèse, Spermatogonies (cytologie), Spermatogonies (métabolisme).
- MESH :
- cytologie : Canalicules séminifères, Cellules souches, Spermatogonies.
- métabolisme : Canalicules séminifères, Cellules souches, Spermatogonies.
- Animaux, Différenciation cellulaire, Haplorhini, Humains, Immunohistochimie, Lignage cellulaire, Mâle, Souris, Spermatogenèse.
English descriptors
- KwdEn :
- MESH :
- cytology : Seminiferous Tubules, Spermatogonia, Stem Cells.
- metabolism : Seminiferous Tubules, Spermatogonia, Stem Cells.
- methods : Immunohistochemistry.
- Animals, Cell Differentiation, Cell Lineage, Haplorhini, Humans, Male, Mice, Spermatogenesis.
Abstract
Spermatogonial stem cells (SSCs) and undifferentiated progenitor spermatogonia in mammalian seminiferous tubules are organized in chains, connected by intracellular bridges. Clone size is generally related to stem cell potential, with shorter chains containing the majority of the stem cell population. Immunofluorescence detection of spermatogonia-specific proteins in whole-mount seminiferous tubule preparations is the only method that allows researchers to relate clone size with the molecular phenotype in spermatogenic lineage development. Here we describe in detail the method used to detect nuclear, cytoplasmic, and cell surface molecules in seminiferous tubules isolated from mouse, monkey, and human testes.
DOI: 10.1007/978-1-4939-1435-7_15
PubMed: 25173170
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Spermatogonial stem cells (SSCs) and undifferentiated progenitor spermatogonia in mammalian seminiferous tubules are organized in chains, connected by intracellular bridges. Clone size is generally related to stem cell potential, with shorter chains containing the majority of the stem cell population. Immunofluorescence detection of spermatogonia-specific proteins in whole-mount seminiferous tubule preparations is the only method that allows researchers to relate clone size with the molecular phenotype in spermatogenic lineage development. Here we describe in detail the method used to detect nuclear, cytoplasmic, and cell surface molecules in seminiferous tubules isolated from mouse, monkey, and human testes.</div>
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<country name="États-Unis"><noRegion><name sortKey="Gassei, Kathrin" sort="Gassei, Kathrin" uniqKey="Gassei K" first="Kathrin" last="Gassei">Kathrin Gassei</name>
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