Morphological analysis of interstitial cells in murine epididymis using light microscopy and transmission electron microscopy.


Journal

Acta histochemica
ISSN: 1618-0372
Titre abrégé: Acta Histochem
Pays: Germany
ID NLM: 0370320

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 09 03 2021
revised: 10 07 2021
accepted: 10 07 2021
pubmed: 24 7 2021
medline: 15 1 2022
entrez: 23 7 2021
Statut: ppublish

Résumé

Smooth muscle contraction of the epididymis plays an important role in sperm transport. Although PDGFRα-positive interstitial cells (PDGFRα (+) ICs) are thought to be involved in controlling smooth muscle movement via intercellular signaling, they have not yet been reported to date in the epididymis. Therefore, we aimed to investigate the morphological characteristics of PDGFRα (+) ICs in the interstitial space of the murine epididymis. Immunohistochemistry showed that PDGFRα (+) ICs co-labeled with CD34 (PDGFRα (+) CD34 (+) ICs were distributed in the interstitial space of the murine epididymis from the initial segment (IS) to the cauda of the epididymis. PDGFRα (+) ICs that were not co-labeled with CD34 (PDGFRα (+) CD34 (-) ICs) were observed just beneath the epithelium from the corpus to the cauda but not in the IS. Both types of PDGFRα (+) ICs were in close proximity to each other as well as the surrounding nerves and macrophages. In addition, PDGFRα (+) CD34 (-) ICs beneath the epithelium were also in close proximity to the basal cells. Using transmission electron microscopy, we identified ICs that possessed elongated and woven cellular processes and were in close proximity to each other, surrounding the cells in the interstitial space. In the murine epididymis, it is suggested that there are two subtypes of ICs that show different distribution patterns depending on the segment, which may reflect segmental differences in mechanisms of sperm transport, forming a cellular network by physical interactions in the murine epididymis.

Identifiants

pubmed: 34298316
pii: S0065-1281(21)00083-0
doi: 10.1016/j.acthis.2021.151761
pii:
doi:

Substances chimiques

Antigens, CD34 0
Receptor, Platelet-Derived Growth Factor alpha EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

151761

Informations de copyright

Copyright © 2021 Elsevier GmbH. All rights reserved.

Auteurs

Tasuku Hiroshige (T)

Division of Microscopic and Developmental Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan; Department of Urology, Kurume University School of Medicine, Kurume, 830-0011, Japan. Electronic address: hiroshige_tasuku@med.kurume-u.ac.jp.

Kei-Ichiro Uemura (KI)

Department of Urology, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Shingo Hirashima (S)

Division of Microscopic and Developmental Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Kiyosato Hino (K)

Division of Microscopic and Developmental Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Akinobu Togo (A)

Advanced Imaging Research Center, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Keisuke Ohta (K)

Advanced Imaging Research Center, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Tsukasa Igawa (T)

Department of Urology, Kurume University School of Medicine, Kurume, 830-0011, Japan.

Kei-Ichiro Nakamura (KI)

Division of Microscopic and Developmental Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.

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Classifications MeSH