Fibroblast growth factor receptor 3 is highly expressed in rarely dividing human type A spermatogonia.

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Fibroblast growth factor receptor 3 is highly expressed in rarely dividing human type A spermatogonia. / von Kopylow, Kathrein; Staege, Hannah; Schulze, Wolfgang; Will, Hans; Kirchhoff, Christiane.

In: HISTOCHEM CELL BIOL, Vol. 138, No. 5, 5, 2012, p. 759-772.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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@article{622e2e48c1d64725a04d5d15cacc3e06,
title = "Fibroblast growth factor receptor 3 is highly expressed in rarely dividing human type A spermatogonia.",
abstract = "Human spermatogonia (Spg) and their fetal precursors express fibroblast growth factor receptor 3 (FGFR3). To further elucidate the role of FGFR3 in the control of Spg self-renewal, proliferation, and/or differentiation, and to narrow down the FGFR3-positive cell type(s) in the normal adult human testis, tissue sections and whole mount preparations of seminiferous tubules were analyzed combining immunofluorescence and confocal fluorescence microscopy. FGFR3 protein was chiefly observed in cellular membranes and cytoplasmic vesicles of a subpopulation of type A Spg, which comprised the chromatin rarefaction zone-containing type A(dark). Cytoplasmic expression of FGFR3 and nuclear expression of proliferation-associated antigen KI-67 were mutually exclusive. Similarly, FGFR3-positive Spg were negative for Doublesex and Mab-3 related transcription factor 1 (DMRT1). By contrast, undifferentiated embryonic cell transcription factor 1 (UTF1) and survival time-associated PHD finger in ovarian cancer 1 protein (SPOC1) were co-expressed in the nuclei of FGFR3-positive Spg. Whole mounted seminiferous tubules illustrated the clonogenic arrangement of the FGFR3/UTF1 double-positive Spg, which mainly occurred as pairs or quadruplets and, different from the KIT-positive Spg, showed no overlap with KI-67 labeled clusters. Taken together, in the adult human testis, FGFR3 expression is a feature of small clones of rarely dividing type A Spg which resemble {"}undifferentiated{"} Spg, including the spermatogonial stem cells.",
keywords = "Humans, Male, Fluorescent Antibody Technique, Microscopy, Confocal, Cell Membrane/metabolism, Testis/cytology/metabolism, *Cell Division, Cytoplasmic Vesicles/metabolism, DNA-Binding Proteins/biosynthesis, Ki-67 Antigen/biosynthesis, Nuclear Proteins/biosynthesis, Proto-Oncogene Proteins c-kit/analysis, Receptor, Fibroblast Growth Factor, Type 3/analysis/*biosynthesis, Seminiferous Tubules/cytology/metabolism, Spermatogenesis/physiology, Spermatogonia/*metabolism, Trans-Activators/biosynthesis, Transcription Factors/analysis/biosynthesis, Humans, Male, Fluorescent Antibody Technique, Microscopy, Confocal, Cell Membrane/metabolism, Testis/cytology/metabolism, *Cell Division, Cytoplasmic Vesicles/metabolism, DNA-Binding Proteins/biosynthesis, Ki-67 Antigen/biosynthesis, Nuclear Proteins/biosynthesis, Proto-Oncogene Proteins c-kit/analysis, Receptor, Fibroblast Growth Factor, Type 3/analysis/*biosynthesis, Seminiferous Tubules/cytology/metabolism, Spermatogenesis/physiology, Spermatogonia/*metabolism, Trans-Activators/biosynthesis, Transcription Factors/analysis/biosynthesis",
author = "{von Kopylow}, Kathrein and Hannah Staege and Wolfgang Schulze and Hans Will and Christiane Kirchhoff",
year = "2012",
language = "English",
volume = "138",
pages = "759--772",
journal = "HISTOCHEM CELL BIOL",
issn = "0948-6143",
publisher = "Springer",
number = "5",

}

RIS

TY - JOUR

T1 - Fibroblast growth factor receptor 3 is highly expressed in rarely dividing human type A spermatogonia.

AU - von Kopylow, Kathrein

AU - Staege, Hannah

AU - Schulze, Wolfgang

AU - Will, Hans

AU - Kirchhoff, Christiane

PY - 2012

Y1 - 2012

N2 - Human spermatogonia (Spg) and their fetal precursors express fibroblast growth factor receptor 3 (FGFR3). To further elucidate the role of FGFR3 in the control of Spg self-renewal, proliferation, and/or differentiation, and to narrow down the FGFR3-positive cell type(s) in the normal adult human testis, tissue sections and whole mount preparations of seminiferous tubules were analyzed combining immunofluorescence and confocal fluorescence microscopy. FGFR3 protein was chiefly observed in cellular membranes and cytoplasmic vesicles of a subpopulation of type A Spg, which comprised the chromatin rarefaction zone-containing type A(dark). Cytoplasmic expression of FGFR3 and nuclear expression of proliferation-associated antigen KI-67 were mutually exclusive. Similarly, FGFR3-positive Spg were negative for Doublesex and Mab-3 related transcription factor 1 (DMRT1). By contrast, undifferentiated embryonic cell transcription factor 1 (UTF1) and survival time-associated PHD finger in ovarian cancer 1 protein (SPOC1) were co-expressed in the nuclei of FGFR3-positive Spg. Whole mounted seminiferous tubules illustrated the clonogenic arrangement of the FGFR3/UTF1 double-positive Spg, which mainly occurred as pairs or quadruplets and, different from the KIT-positive Spg, showed no overlap with KI-67 labeled clusters. Taken together, in the adult human testis, FGFR3 expression is a feature of small clones of rarely dividing type A Spg which resemble "undifferentiated" Spg, including the spermatogonial stem cells.

AB - Human spermatogonia (Spg) and their fetal precursors express fibroblast growth factor receptor 3 (FGFR3). To further elucidate the role of FGFR3 in the control of Spg self-renewal, proliferation, and/or differentiation, and to narrow down the FGFR3-positive cell type(s) in the normal adult human testis, tissue sections and whole mount preparations of seminiferous tubules were analyzed combining immunofluorescence and confocal fluorescence microscopy. FGFR3 protein was chiefly observed in cellular membranes and cytoplasmic vesicles of a subpopulation of type A Spg, which comprised the chromatin rarefaction zone-containing type A(dark). Cytoplasmic expression of FGFR3 and nuclear expression of proliferation-associated antigen KI-67 were mutually exclusive. Similarly, FGFR3-positive Spg were negative for Doublesex and Mab-3 related transcription factor 1 (DMRT1). By contrast, undifferentiated embryonic cell transcription factor 1 (UTF1) and survival time-associated PHD finger in ovarian cancer 1 protein (SPOC1) were co-expressed in the nuclei of FGFR3-positive Spg. Whole mounted seminiferous tubules illustrated the clonogenic arrangement of the FGFR3/UTF1 double-positive Spg, which mainly occurred as pairs or quadruplets and, different from the KIT-positive Spg, showed no overlap with KI-67 labeled clusters. Taken together, in the adult human testis, FGFR3 expression is a feature of small clones of rarely dividing type A Spg which resemble "undifferentiated" Spg, including the spermatogonial stem cells.

KW - Humans

KW - Male

KW - Fluorescent Antibody Technique

KW - Microscopy, Confocal

KW - Cell Membrane/metabolism

KW - Testis/cytology/metabolism

KW - Cell Division

KW - Cytoplasmic Vesicles/metabolism

KW - DNA-Binding Proteins/biosynthesis

KW - Ki-67 Antigen/biosynthesis

KW - Nuclear Proteins/biosynthesis

KW - Proto-Oncogene Proteins c-kit/analysis

KW - Receptor, Fibroblast Growth Factor, Type 3/analysis/biosynthesis

KW - Seminiferous Tubules/cytology/metabolism

KW - Spermatogenesis/physiology

KW - Spermatogonia/metabolism

KW - Trans-Activators/biosynthesis

KW - Transcription Factors/analysis/biosynthesis

KW - Humans

KW - Male

KW - Fluorescent Antibody Technique

KW - Microscopy, Confocal

KW - Cell Membrane/metabolism

KW - Testis/cytology/metabolism

KW - Cell Division

KW - Cytoplasmic Vesicles/metabolism

KW - DNA-Binding Proteins/biosynthesis

KW - Ki-67 Antigen/biosynthesis

KW - Nuclear Proteins/biosynthesis

KW - Proto-Oncogene Proteins c-kit/analysis

KW - Receptor, Fibroblast Growth Factor, Type 3/analysis/biosynthesis

KW - Seminiferous Tubules/cytology/metabolism

KW - Spermatogenesis/physiology

KW - Spermatogonia/metabolism

KW - Trans-Activators/biosynthesis

KW - Transcription Factors/analysis/biosynthesis

M3 - SCORING: Journal article

VL - 138

SP - 759

EP - 772

JO - HISTOCHEM CELL BIOL

JF - HISTOCHEM CELL BIOL

SN - 0948-6143

IS - 5

M1 - 5

ER -