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High hydrostatic pressure treatment of porcine oocytes induces parthenogenetic activation

journal contribution
posted on 06.12.2017, 00:00 by L Lin, C Pribenszky, Gabor Vajta, M Molnár, P Kragh, Y Du, X Zhang, H Yang, L Bolund, H Callesen
An innovative technique called high hydrostatic pressure (HHP) treatment has recently been reported to improve the cryosurvival of gametes and embryos in certain mammalian species, including the mouse, pig, and cattle. In the present study the parthenogenetic activation (PA) of pig oocytes caused by HHP treatment was investigated in different holding media with or without Ca2+. The efficiency of activation was tested at different pressure levels and media including T2 (HEPES-buffered TCM-199 containing 2% cattle serum), and mannitol-PVA fusion medium with (MPVA+Ca2+) or without Ca2+ and Mg2+ (MPVA). The results showed that HHP cannot induce PA in T2, but only in MPVA+Ca2+ with low Ca2+ concentration and MPVA without Ca2+. The highest activation efficiency was achieved with 10 min HHP treatment using 100 or 200 bars for oocytes in MPVA+Ca2+ or MPVA, respectively. In the light of these results, the possible source of Ca2+ during activation was investigated. It was found that even after a total of 30-min wash with TL-HEPES-PVA buffer without Ca2+ before HHP treatment in MPVA, the oocytes could still be activated, indicating the possibility of an intracellular Ca2+ source caused cytoplasmic free Ca2+ elevation. In conclusion, parthenogenetic activation could be induced by HHP in certain holding media with low or zero Ca2+ content. Further experiments are needed to identify the exact mechanisms of activation.

History

Volume

12

Issue

4

Start Page

475

End Page

480

Number of Pages

6

eISSN

2152-4998

ISSN

2152-4971

Location

USA

Publisher

Mary Ann Liebert, Inc.

Language

en-aus

Peer Reviewed

Yes

Open Access

No

External Author Affiliations

Aarhus universitet; BGI-Shenzhen; Purdue University; Szent István Egyetem; TBA Research Institute;

Era Eligible

Yes

Journal

Cellular reprogramming.

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