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Novel Expression of Zona Pellucida 3 Protein in Normal Testis; Potential Functional Implications

Guo Peilan; Makela Juho-Antti; Toppari Jorma; Pulawska Kamila; Huhtaniemi Ilpo; Rahman Nafis A.; Wolczynski Slawomir; Bernaczyk Piotr; Pilaszewicz-Puza Agata; Ponikwicka-Tyszko Donata; Chrusciel Marcin; Leskinen Sini; Lebiedzinska Weronika; Lupu Oana; Li Xiangdong; Coelingh BenninkHerjan J.T.

Novel Expression of Zona Pellucida 3 Protein in Normal Testis; Potential Functional Implications

Guo Peilan
Makela Juho-Antti
Toppari Jorma
Pulawska Kamila
Huhtaniemi Ilpo
Rahman Nafis A.
Wolczynski Slawomir
Bernaczyk Piotr
Pilaszewicz-Puza Agata
Ponikwicka-Tyszko Donata
Chrusciel Marcin
Leskinen Sini
Lebiedzinska Weronika
Lupu Oana
Li Xiangdong
Coelingh BenninkHerjan J.T.
Katso/Avaa
1-s2.0-S0303720721003464-main.pdf (8.192Mb)
Lataukset: 

Elsevier
doi:10.1016/j.mce.2021.111502
URI
https://doi.org/10.1016/j.mce.2021.111502
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022081154460
Tiivistelmä

The expression of the zona pellucida glycoprotein 3 (ZP3), originally thought to be specific for oocytes, was recently extended to ovarian, prostate, colorectal and lung cancers. Earlier successful ZP3 immunization of a transgenic mouse model carrying a ZP3 positive ovarian tumor emphasized the suitability of ZP3 for cancer immunotherapy. This study was carried out to determine whether any other normal tissues besides the ovary in healthy human and mouse tissues may express ZP3, considered important to exclude off-target effects of ZP3 cancer immunotherapy. Strong ZP3 expression was found in normal human and mouse testis. ZP3 protein and mRNA transcripts were localized in spermatogonia, spermatocytes and round and elongated spermatids of both human and mouse testis, as well as in a mouse spermatogonial cell line, but absent in testicular Sertoli, Leydig, spermatogonial stem and progenitor cells. All other normal human and mouse tissues were ZP3 negative. This surprising testicular ZP3 expression has implications for the development of ZP3 cancer immunotherapies, and it also alludes to the potential of using ZP3 as a target for the development of a male immunocontraceptive.

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