Evidence map›Paper›PMID 39153130›Full record

ArticleHistochemistry and cell biology2024

Expression of SARS-CoV-2 entry molecules ACE2, NRP1, TMPRSS2, and FURIN in the reproductive tissues of male macaques.

Ryutaro Moriyama, Sho Nakamura, Ikki Mitsui, Makoto Sugiyama, Hirotaka Fukui, Hitomi Fukui, Teruki Hagiwara, Takako Miyabe-Nishiwaki, Juri Suzuki

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Article in Histochemistry and cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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  3. In focus in HCB.Histochemistry and cell biology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ryutaro MoriyamaDepartment of Life Science, Kindai University, Higashiosaka, Osaka, 577-8502, Japan. mory@life.kindai.ac.jp.ORCID http://orcid.org/0000-0002-5534-8018
Sho NakamuraFaculty of Veterinary Medicine, Okayama University of Science, Imabari, Ehime, 794-8555, Japan.
Ikki MitsuiFaculty of Veterinary Medicine, Okayama University of Science, Imabari, Ehime, 794-8555, Japan.
Makoto SugiyamaFaculty of Veterinary Medicine, Kitasato University School of Veterinary Medicine, Towada, Aomori, 034-8628, Japan.
Hirotaka FukuiFukui Veterinary Hospital, Higashiosaka, Osaka, 577-0809, Japan.
Hitomi FukuiFukui Veterinary Hospital, Higashiosaka, Osaka, 577-0809, Japan.
Teruki HagiwaraDepartment of Life Science, Kindai University, Higashiosaka, Osaka, 577-8502, Japan.
Takako Miyabe-NishiwakiCenter for Human Evolution Modeling Research, Primate Research Institute, Kyoto University, Inuyama, Aichi, 484-8506, Japan.
Juri SuzukiCenter for Human Evolution Modeling Research, Primate Research Institute, Kyoto University, Inuyama, Aichi, 484-8506, Japan.

Funding

A Cooperative Research Program of the Primate Research Institute, Kyoto University 2020-C-18, and 2021-C-1Kindai University R2_Kenkyu-10 and R3_Kenkyu-28
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) reportedly affects male reproductive function by causing spermatogenesis dysfunction and suppressing testosterone secretion. However, the relationship between COVID-19 and impaired reproductive function, such as whether these effects on reproductive function are a direct effect of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection in male reproductive organs or an indirect effect of high fever, is not known. Here, we examined whether the cell entry molecules of SARS-CoV-2, namely, ACE2, NRP1, TMPRSS2, and FURIN, are expressed in the male reproductive organs using the testes and accessory gonads of macaques during the breeding season. RT-PCR expression analysis showed that the testes alone expressed all four molecules. Immunohistochemical staining of testis tissue sections revealed that ACE2 is expressed in Leydig cells and the apical region of Sertoli cells, whereas NRP1 is expressed in the cell bodies surrounding the Leydig and Sertoli cell nuclei. FURIN is mainly expressed in Leydig cells, secondary spermatocytes, and spermatids. However, TMPRSS2 immunopositive cells were not observed. Therefore, it was not possible to observe cells expressing all four molecules in the gonads and accessory gonads of male primates. These results suggest that SARS-CoV-2 is unlikely to directly affect spermatogenesis in primates or proliferate in cells of the seminiferous tubules and undergo release into the semen through the previously known ACE2-mediated infection route. However, the expression of three molecules, including ACE2, was observed in Leydig cells, suggesting that testosterone synthesis and secretion may be affected when primates, including humans, are infected with SARS-CoV-2.

Indexed as

Angiotensin-Converting Enzyme 2FurinNeuropilin-1SARS-CoV-2Serine EndopeptidasesAnimalsCOVID-19Genitalia, MaleMacacaMaleTestisVirus InternalizationAngiotensin-Converting Enzyme 2FurinNeuropilin-1Serine EndopeptidasesACE2COVID-19Leydig cellsMacaqueSARS-CoV-2Testis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.