Organelle reorganization in bovine oocytes during dominant follicle growth and regression
© Dadarwal et al. 2015
Received: 8 September 2015
Accepted: 2 November 2015
Published: 14 November 2015
We tested the hypothesis that organelles in bovine oocytes undergo changes in number and spatial distribution in a manner specific for phase of follicle development.
Cumulus-oocyte-complexes were collected from Hereford heifers by ultrasound-guided follicle aspiration from dominant follicles in the growing phase (n = 5; Day 0 = ovulation), static phase (n = 5), regressing phase (n = 7) of Wave 1 and from preovulatory follicles (n = 5). Oocytes were processed and transmission electron micrographs of ooplasm representing peripheral, perinuclear and central regions were evaluated using standard stereological methods.
The number of mitochondria and volume occupied by lipid droplets was higher (P < 0.03) in oocytes from regressing follicles (193.0 ± 10.4/1000 μm3 and 3.5 ± 0.7 %) than growing and preovulatory stages (118.7 ± 14.4/1000 μm3 and 1.1 ± 0.3 %; 150.5 ± 28.7/1000 μm3 and 1.6 ± 0.2 %, respectively). Oocytes from growing, static and preovulatory follicles had >70 % mitochondria in the peripheral regions whereas oocytes from regressing follicles had an even distribution. Oocytes from growing follicles had more lipid droplets in peripheral region than in central region (86.9 vs. 13.1 %). Percent surface area of mitochondria in contact with lipid droplets increased from growing (2.3 %) to static, regressing or preovulatory follicle stage (8.9, 6.1 and 6.2 %). The amount, size and distribution of other organelles did not differ among phases (P > 0.11).
Our hypothesis was supported in that mitochondrial number increased and translocation occurred from a peripheral to an even distribution as follicles entered the regressing phase. In addition, lipid droplets underwent spatial reorganization from a peripheral to an even distribution during the growing phase and mitochondria-lipid contact area increased with follicle maturation.
Oocyte quality determines the success of fertilization and subsequent embryonic development. Bovine oocytes achieve the competence to sustain fertilization and initial embryonic development to the blastocyst stage by the time the surrounding follicles reach 2–3 mm [1, 2]. The proportion of oocytes that developed to the blastocyst stage was higher for oocytes from follicles >6 mm compared to those from 2 to 6 mm follicles . Similarly, higher blastocyst rates were observed for oocytes obtained from follicles >13 mm compared to those from 5 to 8 mm follicles . In vitro blastocyst rates are reportedly higher for oocytes recovered from well defined static phase compared to the growing and regressing phase of dominant follicle development . Furthermore, higher proportions of blastocyst were reported from in vitro fertilization (IVF) of in vivo matured oocytes (obtained after LH surge) than those matured in-vitro [5, 6]. The follicles (3–8 mm) that were aspirated for in vitro maturation had grown for short duration (1–4 days) compared to follicles that were aspirated after LH surge (6–9 days) [5, 6]. Above-mentioned findings suggest that oocytes undergo maturational changes as the follicle grows. The transcriptional activity of the oocyte is reduced to a minimum by the time a follicle reaches 3 mm in diameter (Fair et al., 1995, 1996), i.e., the follicle stage at the beginning of a follicular wave [7, 8]. Therefore, oocyte processes most likely influenced during follicular selection and dominance are cytoplasmic events such as changes to metabolic pathways, organelle structure and function, and their interactions with each other.
Among cytoplasmic organelles considered crucial for acquisition of oocyte competence, mitochondria and lipid droplets are critical for energy (ATP) production . Moreover, mitochondria and the smooth endoplasmic reticulum (SER) are the primary source of Ca2+ oscillations that govern events such as nuclear maturation, fertilization and activation of embryonic development [10, 11]. The events of nuclear maturation following the preovulatory LH surge have been well characterized by transmission electron microscopy [12–15]. After resumption of meiosis, the majority of the oocytes reach metaphase II at 19–22 h after LH surge . The events of cytoplasmic development before the LH surge during follicular dominance, however, are less studied. The results of an electron microscopy-based qualitative study suggest that structural changes with respect to different organelles occur in the dominant follicle before the LH surge .
Therefore, the objective of the present study was to evaluate structural changes in oocytes obtained from phase-specific dominant follicles by using objective quantitative criteria. Specifically we intended to characterize, quantitatively, the changes in numbers and distribution of mitochondria, lipid droplets, SER within the oocyte at different stages of dominant follicle growth and maturation. We tested the hypothesis that the number and spatial distribution of organelles within the ooplasm change in a phase-specific manner.
Collection of cumulus-oocyte-complexes
Twenty-two crossbred Hereford heifers were maintained in corrals at the Goodale Research Farm, University of Saskatchewan (Saskatoon, Canada). The heifers were between 14 and 22 months of age and had free access to hay, minerals and water. The University Committee on Animal Care and Supply approved the experimental protocol, and the study was conducted in accordance with the guidelines of the Canadian Council on Animal Care.
The COCs were collected using a modified 5 MHz end-fire transvaginal transducer attached to Aloka 500 echocamera as described previously (Brogliatti and Adams 1996). The follicles were aspirated using an 18 gauge, 60 cm long, single-lumen needle with the flow rate of 30 ml/min (Vacuum pump: Allied Healthcare Products, Inc, St Louis, MO, USA). Follicular contents were collected in 15 ml centrifugation tubes containing 3 ml phosphate buffer saline (PBS) with bovine serum albumin (0.2 %) as surfactant and sodium heparin (10 IU/ml) as anticoagulant. The COCs were searched under stereozoom microscope and fixed in 1 % gluteraldehyde and 0.1 M sodium cocodylate buffer (pH 7.4) and stored at 4 °C until further processing for transmission electron microscopy.
Processing of oocytes for transmission electron microscopy
Analyses of cytoplasmic organelle parameters
Quantitative analyses of areas representing peripheral, perinuclear and central ooplasm regions were performed by standard stereological methods that involved random placement of a transparent test-grid (Fig. 2c) over an electron micrograph . The distance between each adjacent cross-points on the grid was 1.5 cm and line lengths were 1.5 cm; therefore the area associated with each cross-point was 2.25 cm2. Peripheral and perinuclear 10 μm regions were identified and demarcated on respective electron micrographs considering that a 1 cm distance on the electron micrograph represented a 1 μm distance within the oocyte (calculated from magnification achieved at printing the electron micrographs). The surface area density (surface area of organelle per unit volume of cytoplasm; μm2/μm3), volume density (volume of organelle per unit volume of cytoplasm; μm3/μm3) and numerical density (number of organelle per unit volume of cytoplasm; number/μm3) were calculated for each organelle [17, 18]. For simplicity, the volume density and numerical density of organelles is presented as percent and number/1000 μm3 of oocyte volume. The points where the lines of the overlay grid intersected the contact between two organelles were used to calculate the contact area and are presented as percent area of mitochondria.
All statistical analyses were done using SAS 9.2 (SAS Institute Inc., Cary, NC, USA). Comparisons among stages of dominant follicle growth were made by one-way analysis of variance. When the regions were compared across the stages of follicle growth, two-way factorial analysis of variance was used. Proportional data were transformed to the arcsine and compared among stages by analysis of variance. The least significant difference was used as a post-hoc test. Data are presented as mean ± standard error (SE) and a P-value ≤0.05 was considered significant. The data for central and perinuclear regions were pooled for the endpoints where significant differences were not observed. The pooled data for central and perinuclear regions was compared with the data for peripheral region for respective endpoints.
Qualitative morphological observations
The oocytes presented a series of typical membrane-bounded organelles (mitochondria, vesicles, SER, Golgi complexes and cortical granules) and lipid droplets (Fig. 2). The mitochondria exhibited two morphologies, hooded and non-hooded (Fig. 2e). Both morphologies were closely associated with SER (Fig. 2f) and lipid droplets (Fig. 2h) as clusters. The vesicles coalesced and became larger as the follicles progressed towards regression.
Volume (percent of ooplasm) and surface density (Mean ± SEM, μm2/μm3 of ooplasm) of mitochondria, SER profiles and vesicles; and number (Mean ± SEM, per 1000 μm3 of ooplasm) of SER profiles and vesicles in oocytes at different stages of follicular development
Preovulatory (D ≥ 17)
Volume (%) (P = 0.04)
2.3 ± 0.2a
2.6 ± 0.3a
3.9 ± 0.5b
2.4 ± 0.4a
Surface Density (μm2/μm3) (P = 0.03)
0.287 ± 0.035a
0.299 ± 0.046a
0.451 ± 0.039b
0.326 ± 0.049a
Volume (%) (P = 0.87)
3.9 ± 0.2
4.9 ± 0.1
4.7 ± 0.8
4.4 ± 0.4
Surface Density (μm2/μm3) (P = 0.34)
0.652 ± 0.065
0.599 ± 0.106
0.780 ± 0.065
0.653 ± 0.055
Number (/1000 μm3) (P = 0.78)
521.5 ± 87.5
467.3 ± 84.9
670.1 ± 85.4
650.2 ± 40.9
Volume (%) (P = 0.42)
20.4 ± 2.9
16.4 ± 1.7
16.2 ± 2.8
21.6 ± 3.2
Surface Density (μm2/μm3) (P = 0.84)
0.972 ± 0.126
0.878 ± 0.073
0.884 ± 0.141
1.005 ± 0.083
Number (/1000 μm3) (P = 0.86)
197.1 ± 33.3
185.8 ± 23.7
254.3 ± 94.4
202.4 ± 9.3
Mitochondrial relation with lipid droplets and SER profiles
The percent surface area of mitochondria in contact with lipid droplets was less (P = 0.04) in the oocytes from growing stage follicles compared to other stages but was not significantly different between other stages (Fig. 3b). In all regions collectively, the percent surface area of mitochondria in contact with SER profiles did not vary (P = 0.42) with the phases of follicle growth (Fig. 3c).
Importantly, the COC in the present study were collected at well-defined phases of dominant follicle development. Oocyte diameter in cattle reaches a plateau by the time antral follicles reach a diameter of 3 mm  but distinct changes in form and function of antral follicles, and presumably the contained oocyte, occur after this developmental stage. The development of ovarian follicles ≥1 mm has been well-characterized using transrectal ultrasonography [20–22] and occurs in a two- or three-wave pattern during the intervoulatory interval [23, 24] Each wave is initiated by a surge in circulating FSH , and the follicles of the cohort grow with equal pace for 2–3 days when all but one follicle begins to slow. At this time of selection, the dominant follicle is around 8.5 mm in size  and attains ovulatory capacity as it acquires LH receptors while other follicles fail to do so . In the presence of a functional corpus luteum and basal circulating LH concentrations, the dominant follicle continues to grow for another 2–3 days and then enters a static phase . After a static phase of about three days, the next follicular wave emerges and the dominant follicle of the previous wave begins a regressing phase. During luteolysis, LH pulsatility increases and the extant dominant follicle continues to grow until the time of ovulation after the LH surge [27, 28]. The competence of the contained oocyte to develop into an embryo increases as the follicle grows [2, 3] and peaks during the late static phase of follicle development . The basis of this increase in oocyte competence has not been fully elucidated, but may be related to changes in cytoplasmic organelle morphology and distribution .
Mitochondria remained in the peripheral ooplasm of oocytes from dominant follicles in the growing, static and preovulatory phases. In previous studies, an even distribution of mitochondria was observed in bovine oocytes of preovulatory follicles ≥19 h after LH surge, when the majority of oocytes had reached MII [12, 15]. None of the oocytes from preovulatory follicles in the present study were at this late stage of meiosis, and we did not observe a translocation of mitochondria to a more even distribution. Interestingly, we noted this even distribution of mitochondria in oocytes from regressing-phase dominant follicles (Fig. 7). As previously described , oocytes from regressing follicles appear to display structural features similar to that of preovulatory oocytes collected after the LH surge. In the present study, two of seven oocytes from regressing follicles exhibited undulations of the nuclear envelop suggesting activation of meiosis. Similar findings were reported elsewhere for the regressing dominant  and subordinate follicles , raising the question about whether the LH surge is requisite for resumption of meiosis. The LH surge has been associated with a build-up of reactive oxygen species (ROS) in the preovulatory follicle, which is required for cumulus cell expansion and ovulation . We speculate that regressing follicles that are undergoing atresia  have increased production of ROS that simulates maturational changes induced by LH in the preovulatory follicle. This may explain why oocytes collected from early regressing follicles may be efficient in sustaining embryonic development upon IVM and IVF .
The increase in the number of mitochondria in our study is attributed specifically to an increase in the number of non-hooded mitochondria. In contrast to results of an earlier report  no changes were detected in the number of hooded mitochondria in the present study. It should be noted, however, that examination of ultra-thin sections would result in an over-estimation of non-hooded mitochondria as hooded mitochondria will appear non-hooded in many sections. The specific roles of the two types of mitochondria are unknown, but some suggest that hooded mitochondria are immature forms that limit the production of reactive oxygen species in the oocyte during maturation and embryonic development (Crocco 2011, Van Blerkom 2004). Others suggest that the hooded morphology increases the functional surface area by extending both outer and inner mitochondrial membranes . Similar to our observations, the hooded type often encircle SER which are crucial for exchange of Ca2+ needed for variety of cell signaling .
Lipid droplets store triglycerides as a source of ATP needed for oocyte maturation and further embryonic development . A previous report indicated an increase in lipid droplet volume as the follicle grow after LH surge and the oocyte progress towards its final maturation . In the present study, an increased lipid content was obvious only when the follicles entered the regressing phase. It is not known why atresia leads to an increased lipid droplet volume per unit of ooplasm in the present study. Interestingly, we have observed bigger lipid droplets in poor quality oocytes obtained from follicles undergoing atresia following superstimulation with FSH starvation . Previously an increase in lipid droplet volume density has been suggested due to an increase in hooded mitochondria that fail to utilize lipid . However, we did not observe any change in the number of hooded mitochondria despite an increase in lipid droplet volume in oocytes as follicles progressed from growing to regressing stages. A close spatial relationship between mitochondria and lipid droplets in oocytes has been reported in cattle [12, 15] and other species . Fluorescence resonance energy transfer analyses of stained mitochondria and lipid droplets in porcine oocytes showed that these two organelles are located within ≤ 10 nm distance to each other that has been considered adequate  for generation of ATP through β-oxidation of lipids, a process that requires carnitine . We speculate that close proximity between mitochondria and lipids during static, regressing and preovulatory phases of dominant follicle development may reflect a greater dependence of the oocytes in these follicles on lipid-derived ATP generation for energy requirements.
Our findings supported previous observation [12, 15] that SER associated vesicles are the most abundant organelle in the oocytes. However, no change in size, number or distribution was observed in the oocytes from follicles of different phases of development in the present study.
Golgi complexes translocate within cytoplasm along microtubules  and are involved in the transport, processing and secretion of proteins, and in the processing of macromolecules following endocytosis [40, 41]. In a recent study of bovine oocytes , these organelles moved from the central to the peripheral ooplasm during germinal vesicle breakdown (GVBD) and back to a central location at the MI stage. In the present study, however, Golgi complexes were located peripherally during the growing phase and centrally during the regressing phase. In the preovulatory follicles, evenly distributed Golgi complexes were (Fig. 7) in accordance with a central movement of these organelles during final oocyte maturation, which in our study did not include GVBD. The difference between studies may be attributed to differences between in vitro maturation conditions  vs. in vivo conditions (present study).
Golgi-derived cortical granules contain the recently identified protease, Ovastacin, which is responsible for cleavage of zona pellucida protein-2 (ZP-2) and preventing polyspermy following fertilization [42, 43]. In previous reports, cortical granules were observed to translocate along microfilaments  from cortical clusters to solitary locations along the oolemma late during final bovine oocyte maturation [13, 15]. In the present study, cortical granules were located peripherally in all phase follicles, but appeared prevalent in oocytes from preovulatory and regressing phase follicles.
Based on the mitochondrial distribution and lipid-mitochondrial contacts it appears that oocytes from growing phase dominant follicles have not yet fully completed the cytoplasmic maturation. At this stage, these oocytes were days away from atresia or ovulation and perhaps have least dependency on ooplasmic lipids for energy demands. We postulate that the oocytes from static phase follicle were morphologically similar to those from preovulatory phase follicles as they had mitochondria in the peripheral region and increased contacts between mitochondrial and lipid droplet compared to other phases. Both static and preovulatory phase follicles have undergone similar period of growth after wave emergence thus it is expected that the cytoplasmic maturation of the contained oocyte will be nearing completion for nuclear maturation and subsequent fertilization, both of which are high energy dependent events. Regression phase follicles have oocytes that has started to undergo atresia (due to loss of dominance) and thus would potentially have less ATP and more ROS generating mitochondria. We hypothesize that mitochondria and lipid droplets redistribution is associated with oocyte’s final attempt to survive. Conversely, cytoplasmic changes observed in the oocytes from early regressing follicles may be reflective of enhanced developmental competence as suggested by earlier studies [12, 29]. Future studies should focus on understanding proposed functional aspects of different organelles (especially mitochondria and lipids) in oocytes from follicles at different phases of follicle development. Such studies would potentially help redesign in vitro embryo production methodology where heterogenous population of follicles is aspirated to obtain oocytes.
We conclude that organelle numbers and distribution patterns occur in a manner specific to the phase of follicular growth, maturation and regression (Fig. 7). Oocytes from follicles in the growing phase displayed the least area of mitochondrial contact with lipid droplets, and a peripheral distribution of lipids. Oocytes from static phase follicle were similar to those from preovulatory phase follicles as they had mitochondria in the peripheral region and increased contacts between mitochondrial and lipid droplet compared to other phases. Oocytes from regressing phase follicles were characterized by an increase in mitochondrial number, and an even distribution of mitochondria. Oocytes from follicles in the regressing phase had greater percent lipid volume than any other phase.
The research was supported by grants from Saskatchewan Agriculture Development Fund and the Natural Sciences and Engineering Research Council of Canada. We are thankful to the staff at the University of Saskatchewan Goodale Farm for the care and management of the cattle.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Blondin P, Sirard MA. Oocyte and follicular morphology as determining characteristics for developmental competence in bovine oocytes. Mol Reprod Dev. 1995;41:54–62.View ArticlePubMedGoogle Scholar
- Lonergan P, Monaghan P, Rizos D, Boland MP, Gordon I. Effect of follicle size on bovine oocyte quality and developmental competence following maturation, fertilization, and culture in vitro. Mol Reprod Dev. 1994;37:48–53.View ArticlePubMedGoogle Scholar
- Hagemann LJ, Beaumont SE, Berg M, Donnison MJ, Ledgard A, Peterson AJ, et al. Development during single IVP of bovine oocytes from dissected follicles: interactive effects of estrous cycle stage, follicle size and atresia. Mol Reprod Dev. 1999;53:451–8.View ArticlePubMedGoogle Scholar
- Vassena R, Mapletoft RJ, Allodi S, Singh J, Adams GP. Morphology and developmental competence of bovine oocytes relative to follicular status. Theriogenology. 2003;60:923–32.View ArticlePubMedGoogle Scholar
- Hendriksen PJ, Vos PL, Steenweg WN, Bevers MM, Dieleman SJ. Bovine follicular development and its effect on the in vitro competence of oocytes. Theriogenology. 2000;53:11–20.View ArticlePubMedGoogle Scholar
- van de Leemput EE, Vos PL, Zeinstra EC, Bevers MM, van der Weijden GC, Dieleman SJ. Improved in vitro embryo development using in vivo matured oocytes from heifers superovulated with a controlled preovulatory LH surge. Theriogenology. 1999;52:335–49.View ArticlePubMedGoogle Scholar
- Ginther OJ, Knopf L, Kastelic JP. Temporal associations among ovarian events in cattle during oestrous cycles with two and three follicular waves. J Reprod Fertil. 1989;87:223–30.View ArticlePubMedGoogle Scholar
- Adams GP, Singh J. Ovarian follicular and luteal dynamics in cattle. In: Hopper RM, editor. Bovine Reproduction. 1st ed. Iowa, USA: John Wiley and Sons Inc; 2015.Google Scholar
- Dunning KR, Cashman K, Russell DL, Thompson JG, Norman RJ, Robker RL. Beta-oxidation is essential for mouse oocyte developmental competence and early embryo development. Biol Reprod. 2010;83:909–18.View ArticlePubMedGoogle Scholar
- Ajduk A, Małagocki A, Maleszewski M. Cytoplasmic maturation of mammalian oocytes: development of a mechanism responsible for sperm-induced Ca2+ oscillations. Reprod Biol. 2008;8:3–25.View ArticlePubMedGoogle Scholar
- Machaca K. Ca2+ signaling differentiation during oocyte maturation. J Cell Physiol. 2007;213:331–71.View ArticlePubMedGoogle Scholar
- Assey RJ, Hyttel P, Greve T, Purwantara B. Oocyte morphology in dominant and subordinate follicles. Mol Reprod Dev. 1994;37:335–44.View ArticlePubMedGoogle Scholar
- Hyttel P, Xu KP, Smith S, Greve T. Ultrastructure of in-vitro oocyte maturation in cattle. J Reprod Fertil. 1986;78:615–25.View ArticlePubMedGoogle Scholar
- Hyttel P, Xu KP, Smith S, Callesen H, Greve T. Ultrastructure of the final nuclear maturation of bovine oocytes in vitro. Anat Embryol (Berl). 1987;176:35–40.View ArticleGoogle Scholar
- Kruip TAM, Cran DG, van Beneden TH, Dieleman SJ. Structural changes in bovine oocytes during final maturation in vivo. Gamete Res. 1983;8:29–47.View ArticleGoogle Scholar
- Weibel ER, Kistler GS, Scherle WF. Practical stereological methods for morphometric cytology. J Cell Biol. 1966;30:23–38.PubMed CentralView ArticlePubMedGoogle Scholar
- Zoller LC. A quantitative electron microscopic analysis of the membrana granulosa of rat preovulatory follicles. Acta Anat. 1984;118:218–23.View ArticlePubMedGoogle Scholar
- Baddeley AJ, Gundersen HJ, Cruz-Orive LM. Estimation of surface area from vertical sections. J Micros. 1986;142:259–76.View ArticleGoogle Scholar
- Fair T. Follicular oocyte growth and acquisition of developmental competence. Anim Reprod Sci. 2003;78:203–16.View ArticlePubMedGoogle Scholar
- Jaiswal RS, Singh J, Adams GP. Developmental pattern of small antral follicles in the bovine ovary. Biol Reprod. 2004;71:1244–51.View ArticlePubMedGoogle Scholar
- Savio JD, Keenan L, Boland MP, Roche JF. Pattern of growth of dominant follicles during the oestrous cycle of heifers. J Reprod Fertil. 1988;83:663–71.View ArticlePubMedGoogle Scholar
- Knopf L, Kastelic JP, Schallenberger E, Ginther OJ. Ovarian follicular dynamics in heifers: test of two-wave hypothesis by ultrasonically monitoring individual follicles. Domest Anim Endocrinol. 1989;6:111–9.View ArticlePubMedGoogle Scholar
- Adams GP, Singh J, Baerwald AR. Large animal models for the study of ovarian follicular dynamics in women. Theriogenology. 2012;78:1733–48.View ArticlePubMedGoogle Scholar
- Jaiswal RS, Singh J, Marshall L, Adams GP. Repeatability of 2-wave and 3-wave patterns of ovarian follicular development during the bovine estrous cycle. Theriogenology. 2009;72:81–90.View ArticlePubMedGoogle Scholar
- Adams GP, Matteri RL, Kastelic JP, Ko JC, Ginther OJ. Association between surges of follicle-stimulating hormone and the emergence of follicular waves in heifers. J Reprod Fertil. 1992;94:177–88.View ArticlePubMedGoogle Scholar
- Bao B, Garverick HA, Smith GW, Smith MF, Salfen BE, Youngquist RS. Changes in messenger ribonucleic acid encoding luteinizing hormone receptor, cytochrome P450-side chain cleavage, and aromatase are associated with recruitment and selection of bovine ovarian follicles. Biol Reprod. 1997;56:1158–68.View ArticlePubMedGoogle Scholar
- Rathbone MJ, Kinder JE, Fike K, Kojima F, Clopton D, Ogle CR, et al. Recent advances in bovine reproductive endocrinology and physiology and their impact on drug delivery system design for the control of the estrous cycle in cattle. Advanc Drug Del Rev. 2001;50:277–320.View ArticleGoogle Scholar
- Ginther OJ, Khan FA, Hannan MA, Rodriguez MB, Pugliesi G, Beg MA. Role of LH in luteolysis and growth of the ovulatory follicle and estradiol regulation of LH secretion in heifers. Theriogenology. 2012;77:1442–52.View ArticlePubMedGoogle Scholar
- Salamone DF, Adams GP, Mapletoft RJ. Changes in the cumulus-oocyte complex of subordinate follicles relative to follicular wave status in cattle. Theriogenology. 1999;52:549–61.View ArticlePubMedGoogle Scholar
- Shkolnik K, Tadmor A, Ben-Dor S, Nevo N, Galiani D, Dekel N. Reactive oxygen species are indispensable in ovulation. Proc Natl Acad Sci U S A. 2011;108:1462–9.PubMed CentralView ArticlePubMedGoogle Scholar
- Singh J, Adams GP. Histomorphometry of dominant and subordinate bovine ovarian follicles. Anat Rec. 2000;258:58–70.View ArticlePubMedGoogle Scholar
- Fair T, Hulshof SC, Hyttel P, Greve T, Boland M. Oocyte ultrastructure in bovine primordial to early tertiary follicles. Anat Embryol. 1997;195:327–36.View ArticlePubMedGoogle Scholar
- Senger PL, Saacke RG. Unusual mitochondria of the bovine oocyte. J Cell Biol. 1970;46:405–8.PubMed CentralView ArticlePubMedGoogle Scholar
- Iino M. Spatiotemporal dynamics of Ca 2+ signaling and its physiological roles. Proc Jpn Acad. 2010;86:244–56.View ArticleGoogle Scholar
- Sturmey RG, O’Toole PJ, Leese HJ. Fluorescence resonance energy transfer analysis of mitochondrial:lipid association in the porcine oocyte. Reproduction. 2006;132:829–37.View ArticlePubMedGoogle Scholar
- Dadarwal D, Honparkhe M, Dias FC, Alce T, Lessard C, Singh J. Effect of superstimulation protocols on nuclear maturation and distribution of lipid droplets in bovine oocytes. Reprod Fertil Dev 2014. doi:10.1071/RD13265.
- Crosier AE, Farin PW, Dykstra MJ, Alexander JE, Farin CE. Ultrastructural morphometry of bovine compact morulae produced in vivo or in vitro. Biol Reprod. 2000;62:1459–65.View ArticlePubMedGoogle Scholar
- Cran DG. Qualitative and quantitative structural changes during pig oocyte maturation. J Reprod Fertil. 1985;74:237–45.View ArticlePubMedGoogle Scholar
- Racedo S, Rawe V, Niemann H. Dynamic changes of the Golgi apparatus during bovine in vitro oocyte maturation. Reproduction. 2012;143:439–86.View ArticlePubMedGoogle Scholar
- Rothman J. Mechanisms of intracellular protein transport. Nature. 1994;372:55–118.View ArticlePubMedGoogle Scholar
- Allan B, Balch W. Protein sorting by directed maturation of Golgi compartments. Science (New York, NY). 1999;285:63–9.View ArticleGoogle Scholar
- Burkart A, Xiong B, Baibakov B, Jimenez-Movilla M, Dean J. Ovastacin, a cortical granule protease, cleaves ZP2 in the zona pellucida to prevent polyspermy. J Cell Biol. 2012;197:37–81.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu M. The biology and dynamics of mammalian cortical granules. Reprod Biol Endo. 2011;9:149.View ArticleGoogle Scholar
- Glater EE, Megeath LJ, Stowers RS, Schwarz TL. Axonal transport of mitochondria requires milton to recruit kinesin heavy chain and is light chain independent. J Cell Biol. 2006;173:545–57.PubMed CentralView ArticlePubMedGoogle Scholar