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Characterization of Mammalian ADAM2 and Its Absence from Human Sperm
The members of the ADAM (a disintegrin and metalloprotease) family are membrane-anchored multi-domain proteins that play prominent roles in male reproduction. ADAM2, which was one of the first identified ADAMs, is the best studied ADAM in reproduction. In the male germ cells of mice, ADAM2 and other...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920383/ https://www.ncbi.nlm.nih.gov/pubmed/27341348 http://dx.doi.org/10.1371/journal.pone.0158321 |
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author | Choi, Heejin Jin, Sora Kwon, Jun Tae Kim, Jihye Jeong, Juri Kim, Jaehwan Jeon, Suyeon Park, Zee Yong Jung, Kang-Jin Park, Kwangsung Cho, Chunghee |
author_facet | Choi, Heejin Jin, Sora Kwon, Jun Tae Kim, Jihye Jeong, Juri Kim, Jaehwan Jeon, Suyeon Park, Zee Yong Jung, Kang-Jin Park, Kwangsung Cho, Chunghee |
author_sort | Choi, Heejin |
collection | PubMed |
description | The members of the ADAM (a disintegrin and metalloprotease) family are membrane-anchored multi-domain proteins that play prominent roles in male reproduction. ADAM2, which was one of the first identified ADAMs, is the best studied ADAM in reproduction. In the male germ cells of mice, ADAM2 and other ADAMs form complexes that contribute to sperm-sperm adhesion, sperm-egg interactions, and the migration of sperm in the female reproductive tract. Here, we generated specific antibodies against mouse and human ADAM2, and investigated various features of ADAM2 in mice, monkeys and humans. We found that the cytoplasmic domain of ADAM2 might enable the differential association of this protein with other ADAMs in mice. Western blot analysis with the anti-human ADAM2 antibodies showed that ADAM2 is present in the testis and sperm of monkeys. Monkey ADAM2 was found to associate with chaperone proteins in testis. In humans, we identified ADAM2 as a 100-kDa protein in the testis, but failed to detect it in sperm. This is surprising given the results in mice and monkeys, but it is consistent with the failure of ADAM2 identification in the previous proteomic analyses of human sperm. These findings suggest that the reproductive functions of ADAM2 differ between humans and mice. Our protein analysis showed the presence of potential ADAM2 complexes involving yet-unknown proteins in human testis. Taken together, our results provide new information regarding the characteristics of ADAM2 in mammalian species, including humans. |
format | Online Article Text |
id | pubmed-4920383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49203832016-07-18 Characterization of Mammalian ADAM2 and Its Absence from Human Sperm Choi, Heejin Jin, Sora Kwon, Jun Tae Kim, Jihye Jeong, Juri Kim, Jaehwan Jeon, Suyeon Park, Zee Yong Jung, Kang-Jin Park, Kwangsung Cho, Chunghee PLoS One Research Article The members of the ADAM (a disintegrin and metalloprotease) family are membrane-anchored multi-domain proteins that play prominent roles in male reproduction. ADAM2, which was one of the first identified ADAMs, is the best studied ADAM in reproduction. In the male germ cells of mice, ADAM2 and other ADAMs form complexes that contribute to sperm-sperm adhesion, sperm-egg interactions, and the migration of sperm in the female reproductive tract. Here, we generated specific antibodies against mouse and human ADAM2, and investigated various features of ADAM2 in mice, monkeys and humans. We found that the cytoplasmic domain of ADAM2 might enable the differential association of this protein with other ADAMs in mice. Western blot analysis with the anti-human ADAM2 antibodies showed that ADAM2 is present in the testis and sperm of monkeys. Monkey ADAM2 was found to associate with chaperone proteins in testis. In humans, we identified ADAM2 as a 100-kDa protein in the testis, but failed to detect it in sperm. This is surprising given the results in mice and monkeys, but it is consistent with the failure of ADAM2 identification in the previous proteomic analyses of human sperm. These findings suggest that the reproductive functions of ADAM2 differ between humans and mice. Our protein analysis showed the presence of potential ADAM2 complexes involving yet-unknown proteins in human testis. Taken together, our results provide new information regarding the characteristics of ADAM2 in mammalian species, including humans. Public Library of Science 2016-06-24 /pmc/articles/PMC4920383/ /pubmed/27341348 http://dx.doi.org/10.1371/journal.pone.0158321 Text en © 2016 Choi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Choi, Heejin Jin, Sora Kwon, Jun Tae Kim, Jihye Jeong, Juri Kim, Jaehwan Jeon, Suyeon Park, Zee Yong Jung, Kang-Jin Park, Kwangsung Cho, Chunghee Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title | Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title_full | Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title_fullStr | Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title_full_unstemmed | Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title_short | Characterization of Mammalian ADAM2 and Its Absence from Human Sperm |
title_sort | characterization of mammalian adam2 and its absence from human sperm |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920383/ https://www.ncbi.nlm.nih.gov/pubmed/27341348 http://dx.doi.org/10.1371/journal.pone.0158321 |
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