The Loss of Polysialic Acid Impairs the Contractile Phenotype of Peritubular Smooth Muscle Cells in the Postnatal Testis.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
29 05 2021
Historique:
received: 19 11 2020
revised: 07 05 2021
accepted: 17 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 11 2021
Statut: epublish

Résumé

In the testis, the germinal epithelium of seminiferous tubules is surrounded by contractile peritubular cells, which are involved in sperm transport. Interestingly, in postnatal testis, polysialic acid (polySia), which is also an essential player for the development of the brain, was observed around the tubules. Western blotting revealed a massive decrease of polySia from postnatal day 1 towards puberty, together with a fundamental reduction of the net-like intertubular polySia. Using polysialyltransferase knockout mice, we investigated the consequences of the loss of polySia in the postnatal testis. Compared to postnatal wild-type animals, polySia knockouts showed slightly reduced smooth muscle actin (SMA) immunostaining of peritubular smooth muscle cells (SMCs), while calponin, marking more differentiated SMCs, dramatically decreased. In contrast, testicular SMA and calponin immunostaining remained unchanged in vascular SMCs in all genotypes. In addition, the cGMP-dependent protein kinase PKG I, a key enzyme of SMC relaxation, was nearly undetectable in the peritubular SMCs. Cell proliferation in the peritubular layer increased significantly in the knockouts, as shown by proliferating cell nuclear anti (PCNA) staining. Taken together, in postnatal testis, the absence of polySia resulted in an impaired differentiation of peritubular, but not vascular, SMCs to a more synthetic phenotype. Thus, polySia might influence the maintenance of a differentiated phenotype of non-vascular SMCs.

Identifiants

pubmed: 34072405
pii: cells10061347
doi: 10.3390/cells10061347
pmc: PMC8230264
pii:
doi:

Substances chimiques

Sialic Acids 0
polysialic acid 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Nadim E Hachem (NE)

Department of Anatomy and Cell Biology, Medical Faculty, Justus-Liebig-University, Aulweg 123, 35385 Giessen, Germany.

Luisa Humpfle (L)

Department of Anatomy and Cell Biology, Medical Faculty, Justus-Liebig-University, Aulweg 123, 35385 Giessen, Germany.

Peter Simon (P)

Institute of Biochemistry, Medical Faculty, Justus-Liebig-University, Friedrichstr. 24, 35392 Giessen, Germany.

Miriam Kaese (M)

Institute of Biochemistry, Medical Faculty, Justus-Liebig-University, Friedrichstr. 24, 35392 Giessen, Germany.

Birgit Weinhold (B)

Institute of Clinical Biochemistry, OE 4340, Hannover Medical School, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

Juliane Günther (J)

Institute of Reproductive Biology, Leibniz Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196 Dummerstorf, Germany.

Sebastian P Galuska (SP)

Institute of Biochemistry, Medical Faculty, Justus-Liebig-University, Friedrichstr. 24, 35392 Giessen, Germany.
Institute of Reproductive Biology, Leibniz Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196 Dummerstorf, Germany.

Ralf Middendorff (R)

Department of Anatomy and Cell Biology, Medical Faculty, Justus-Liebig-University, Aulweg 123, 35385 Giessen, Germany.

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