Reversible Disassembly of the Actin Cytoskeleton Improves the Survival Rate and Developmental Competence of Cryopreserved Mouse Oocytes

被引:28
作者
Hosu, Basarab G. [1 ]
Mullen, Steven F. [2 ]
Critser, John K. [4 ]
Forgacs, Gabor [3 ,4 ,5 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA USA
[2] 21st Century Med, Fontana, CA USA
[3] Univ Missouri, Dept Biol Sci, Columbia, MO USA
[4] Univ Missouri, Dept Vet Pathobiol, Columbia, MO USA
[5] Univ Missouri, Dept Phys, Columbia, MO USA
关键词
D O I
10.1371/journal.pone.0002787
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Effective cryopreservation of oocytes is critically needed in many areas of human reproductive medicine and basic science, such as stem cell research. Currently, oocyte cryopreservation has a low success rate. The goal of this study was to understand the mechanisms associated with oocyte cryopreservation through biophysical means using a mouse model. Specifically, we experimentally investigated the biomechanical properties of the ooplasm prior and after cryopreservation as well as the consequences of reversible dismantling of the F-actin network in mouse oocytes prior to freezing. The study was complemented with the evaluation of post-thaw developmental competence of oocytes after in vitro fertilization. Our results show that the freezing-thawing process markedly alters the physiological viscoelastic properties of the actin cytoskeleton. The reversible depolymerization of the F-actin network prior to freezing preserves normal ooplasm viscoelastic properties, results in high post-thaw survival and significantly improves developmental competence. These findings provide new information on the biophysical characteristics of mammalian oocytes, identify a pathophysiological mechanism underlying cryodamage and suggest a novel cryopreservation method.
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页数:9
相关论文
共 59 条
[1]
Albertini D, 2004, ESSENTIAL IVF: BASIC RESEARCH AND CLINICAL APPLICATIONS, P43
[2]
Measurement of local viscoelasticity and forces in living cells by magnetic tweezers [J].
Bausch, AR ;
Möller, W ;
Sackmann, E .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :573-579
[3]
DEVELOPMENT OF PRE-IMPLANTATION EMBRYOS OF THE GOLDEN-HAMSTER IN A DEFINED CULTURE-MEDIUM [J].
BAVISTER, BD ;
LEIBFRIED, ML ;
LIEBERMAN, G .
BIOLOGY OF REPRODUCTION, 1983, 28 (01) :235-247
[4]
Cryopreservation of human oocytes: A review of current problems and perspectives [J].
Bernard, A ;
Fuller, BJ .
HUMAN REPRODUCTION UPDATE, 1996, 2 (03) :193-207
[5]
BIGGERS JD, 1972, OOGENESIS
[6]
Cytoskeletal remodelling and slow dynamics in the living cell [J].
Bursac, P ;
Lenormand, G ;
Fabry, B ;
Oliver, M ;
Weitz, DA ;
Viasnoff, V ;
Butler, JP ;
Fredberg, JJ .
NATURE MATERIALS, 2005, 4 (07) :557-561
[7]
Use of fluorescence in situ hybridization to assess the chromosomal status of embryos obtained from cryopreserved oocytes [J].
Cobo, A ;
Rubio, C ;
Gerli, S ;
Ruiz, A ;
Pellicer, A ;
Remohí, J .
FERTILITY AND STERILITY, 2001, 75 (02) :354-360
[8]
THE PHYSICAL PROPERTIES OF CYTOPLASM - A STUDY BY MEANS OF THE MAGNETIC PARTICLE METHOD .1. EXPERIMENTAL [J].
CRICK, FHC ;
HUGHES, AFW .
EXPERIMENTAL CELL RESEARCH, 1950, 1 (01) :37-80
[9]
Micro magnetic tweezers for nanomanipulation inside live cells [J].
de Vries, AHB ;
Krenn, BE ;
van Driel, R ;
Kanger, JS .
BIOPHYSICAL JOURNAL, 2005, 88 (03) :2137-2144
[10]
Birth of piglets after transfer of embryos cryopreserved by cytoskeletal stabilization and vitrification [J].
Dobrinsky, JR ;
Pursel, VG ;
Long, CR ;
Johnson, LA .
BIOLOGY OF REPRODUCTION, 2000, 62 (03) :564-570