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Effects of trichostatin A on cumulus expansion during mouse oocyte maturation.

INTRODUCTION

Cumulus expansion is a highly coordinated process that facilitates the release of the oocyte into the abdominal cavity, capture of the oocyte by the oviductal fimbria, and fertilization (Dragovic et al., 2005). Cumulus expansion is a critical physiological process, as impaired expansion leads to sterility (Fulop et al., 2003). Expansion of the mouse cumulus-oocyte complexes (COCs) is critically dependent upon two signaling events: i) stimulation by gonadotropins or epidermal growth factors (EGFs) and ii) paracrine signals secreted by the oocyte, termed cumulus expansion-enabling factors (CEEFs), which act on neighboring cumulus cells, enabling these cells to respond to the aforementioned stimuli (Buccione et al., 1990; Vanderhyden et al., 1990; Dragovic et al., 2007).

GDF9, a member of the transforming growth factor p (TGF[beta]) superfamily of protein signaling molecules, shares sequence homology and predicted structural homology with bone morphogenetic proteins (BMPs) (McPherron et al., 1993). In rodents, GDF9 is produced primarily in the ovaries and is localized exclusively to oocytes in growing follicles (Hayashi et al., 1999). Moreover, GDF9 was the first oocyte-specific factor shown to be essential for cumulus expansion (Elvin et al., 1999). Deletion of GDF9 results in female results in sterility due to impair follicular development. In these mice, all follicles are arrested at the the primary follicle stage (Dong et al., 1996). GDF9 represents one of several key CEEFs that serve as key mediators that promoting cumulus expansion in the mouse (Gui et al., 2005).

Cumulus expansion stimulated by a ligand (FSH or EGF) and CEEFs is associated with elevated levels of extracellular matrix (ECM) genes (Has2, Ptgs2, Ptx3, and Tnfaip6) in cumulus cells (Ochsner et al., 2003; Su et al., 2003; Salustri et al., 2004). Hyaluronan synthase 2 (HAS2) is the key enzyme required for the production of hyaluronic acid, a non-sulfated glycosaminoglycan secreted by cumulus cells. Non-sulfated glyosaminoglacycan is a fundamental component of the cumulus matrix (Camaioni et al., 1993; Chen et al., 1993). Prostaglandin synthase 2 (PTGS2, also known as COX2, cyclooxygenase 2), the product of cumulus cells and granulosa cells, is required for maximum cumulus expansion and ovulation (Lim et al., 1997). Tumor necrosis factor-induced protein 6 (TNFAIP6, also known as TSG6), is a secreted protein that binds hyaluronic acid and inter-[alpha] trypsin inhibitor (ITI), which is a serum-derived protein important for matrix formation. TSG6 binding cross-links ITI heavy chains to hyaluronic acid (Fulop et al., 2003; Mukhopadhyay et al., 2004). Pentraxin 3 (PTX3), is also secreted by cumulus cells and acts to stabilize TNFAIP6 protein to maintain the expanded matrix (Salustri et al., 2004; Varani et al., 2002). In addition to extracellular matrix, intracellular signaling cascades play crucial roles in controlling by gonadotropins and growth factors-induced cumulus expansion. For example, mitogen-activated protein kinase activity mediates gonadotropin response in mouse cumulus cells. Inhibition of MEK activation using pharmacologically inhibitor U0126 blocks GDF9-induced cumulus expansion and suppress the expression of ECM genes (Su et al., 2002).

Despite of these important findings, our understanding of transcriptional regulation of gene expression in cumulus cells during oocyte maturation remains limited. In general, histone hyper-acetylation is associated with transcriptional activation, and in contrast, histone hypo-acetylation is indicative of transcriptional repression (Barter et al., 2010). However, in large-scale gene studies, a significant number of genes are down-regulated when HDAC activity is inhibited (Xu et al., 2007). Trichostatin A (TSA), a fermentation product of Streptomyces, is widely used as a non-selective general histone deacetylase (HDAC) inhibitor to study gene regulation in animal cells (Tsuji et al., 1976). For example, TSA and sodium butyrate (NaB) treatment cause reductions in the mRNA levels of the cdk1 gene (Saunders et al., 1999). Furthermore, TSA represses p-casein expression in mammary epithelial cells (Pujuguet et al., 2001), TSA represses the cyclins B1 and A (Nair et al., 2001), and TSA inhibits mouse mammary tumor virus (MMTV) transcription (Mulholland et al., 2003). Based on previous reports, we hypothesized that inhibition of histone acetylation with TSA may inhibit cumulus expansion and change expression of cumulus expansion-related genes. To verify this hypothesis, we investigated the effects of TSA on cumulus expansion during oocyte maturation by assaying the expression of related genes and proteins.

MATERIALS AND METHODS

All chemicals and media were purchased from Sigma Chemical Co. (St. Louis, MO) unless otherwise indicated. The animals used in this study were 22-24-d-old Kunming white mice (Academy of Military Medical Sciences, Beijing, China) that were maintained at 20-22[degrees]C on a 14 h (6:00 to 20:00) light and 10 h (20:00 to 6:00) dark schedule. The experimental protocols for handing the mice were in accordance with the guidelines of the Institutional Animal Care and Use Committee of the China Agricultural University.

Cell isolation and culture

Female mice were injected with 10 IU eCG (Ningbo Hormone Products CO., China) for 46 to 48 h to stimulate follicular development. COCs and fully grown oocytes (FGOs) were then isolated as previously described (Su et al., 2008). Microsurgical removal of oocytes from the COCs was carried out as previously described (Dragovic et al., 2007). The resulting oocytectomized complex (OOX) consisted of the spherical zona pellucida, surrounded by the cumulus cell mass, but was deprived of the oocyte. The culture medium used for all of the experiments was Waymouth's MB752/1 Medium (Life Technologies, Inc., Grand Island, NY) with 10 ng/mL epidermal growth factor (EGF), 10 milrinone, 75 mg/L penicillin G, 50 mg/L streptomycin sulfate, 0.23 mM pyruvate, and 5% fetal bovine serum (FBS). All of the cultures were maintained at 37[degrees] C 5% C[O.sub.2] in air with maximum humidity. The cells were cultured for various periods of time, according to each experimental design and were then harvested for RNA or protein extraction.

Cumulus expansion experiment

COCs and OOX cumulus cells+FGOs (two FGOs/[micro]L of medium) were cultured in a drop of medium covered with mineral oil at a density of one COC or OOX cumulus cell/[micro]L of medium in a 35-mm diameter plastic Petri dish (Nuclon, Rochester, NY) for 15 h. TSA was added to the culture medium in the treatment group. The concentration of TSA (100 nM) was determined as described previously (Suo et al., 2010). The FGOs and OOX were pretreated with 100 nM TSA for 30 min or 4 h and were then co-cultured with the OOX and FGOs for 15 h, respectively. The experimental design is shown in Table 1. The degree of cumulus expansion was scored after 15 h of culture according to a subjective scale ranging from 0 (no expansion) to 4 (complete expansion), and a cumulus expansion index (CEI) was calculated (range, 0 to 4.00), as described previously (Fagbohun et al., 1990; Vanderhyden et al., 1990).

cDNA preparation and real-time PCR analysis

Total RNA was isolated and was treated with DNase I to eliminate the DNA contamination. cDNA was synthesized using an Ambion Cells-to-cDNA II kit (Life Technologies, Inc., Grand Island, NY) with MMLV reverse transcriptase and random hexamers, following the manufacturer's instructions. Real-time PCR analyses were conducted as described previously (Su et al., 2008) to quantify the mRNA levels of Has2, Ptx3, Ptgs2, Tnfaip6, and GDF9 and the housekeeping gene Rpl19 (internal control). The primer sequences for Has2, Ptx3, Ptgs2, Tnfaip6, GDF9, and Rpl19 are listed in Table 2. Calculation of the relative fold change in the levels of Has2, Ptx3, Ptgs2, Tnfaip6, and GDF9 was performed using the [2-.sup.[DELTA][DELTA]Ct] method, as previously described (Su et al., 2007). For each experiment, the levels of Has2, Ptx3, Ptgs2, Tnfaip6, or GDF9 mRNA are presented as relative changes compared to a specific group (internal control) in which the expression level was set at 1. All the experiments were repeated three times, and data were presented as mean [+ or -] SEM.

Western blot

Protein samples from 100 FGOs or cumulus cells from 50 OOX were prepared, and Western blot analysis was performed as described previously (Su et al., 2001). The phosphorylated forms of MAPK were detected using a monoclonal anti-MAPK activated (diphosphorylated ERK-1 and -2) antibody. The secondary antibody used for the detection of the MAPK primary antibody complex was horseradish peroxidase-conjugated goat anti mouse IgG. Proteins on the membrane were visualized using an ECL detection system (Pierce Chemical Co., Rockford, IL). After the initial analysis, the membranes were washed in a stripping buffer (Pierce Chemical Co. Rockford, IL) to remove bound antibodies and were reprobed with a polyclonal anti-MAPK antibody to detect the total amount of MAPK (phosphorylated and unphosphorylated forms). The second antibody used in the reprobing was horseradish peroxidase-conjugated goat anti rabbit IgG (Sigma). The actin primary antibody was a mouse monoclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA). The GDF-9 primary antibody was a goat polyclonal antibody generated against a synthetic peptide based on the mouse GDF-9 sequence (Santa Cruz Biotechnology, Santa Cruz, CA), and a donkey anti-goat IgG-horseradish peroxidase conjugate (Santa Cruz Biotechnology) was used as the secondary antibody.

Statistical analysis

All of the experiments were performed independently at least three times. Data were analyzed using one-way ANOVA and Duncan's test for mean differences (p<0.05) in SPSS 17.0. The results are expressed as the mean+standard error of the mean (SEM).

RESULTS

Effect of TSA on cumulus expansion

As shown in Figure 1, cumulus expansion did not occur in the group treated with 100 nM TSA (Figure 1-I, II). The corresponding CEI of group I (3.93 [+ or -] 0.01) was significantly higher than that of group II (0.83 [+ or -] 0.04) (Figure 1A, p<0.05). TSA treatment inhibited cumulus expansion in the OOX and FGO co-cultured groups (groups III and IV) (Figure 1-III, IV). The corresponding CEI of group III (3.84 [+ or -] 0.02) was significantly higher than that of group IV (0.77 [+ or -] 0.03) (Figure 1A, p<0.05). The FGOs and OOX were pretreated with 100 nM TSA for 30 min or 4 h and were then co-cultured with OOX or FGOs, respectively, for 15 h. The CEIs of groups V (3.1 [+ or -] 0.04) and VII (3.0 [+ or -] 0.04) were significantly higher than those of groups VI (1.87 [+ or -] 0.04) and VIII (1.81 [+ or -] 0.03) (Figure 1A, p<0.05), indicating that cumulus expansion in groups V and VII (Figure 1-V, VII) was greater than in groups VI and VIII (Figure 1-VI, VIII).

Effect of TSA on ECM (Has2, Ptgs2, Ptx3, and Tnfaip6) and GDF9 gene expression

The mRNA levels of the cumulus expansion-related genes Has2, Ptgs2, Ptx3, and Tnfaip6 and the expression level of GDF9 were detected. As shown in Figrue 2A to D, the mRNA levels of Has2, Ptgs2, Ptx3, and Tnfaip6 in groups II, IV, VI, and VIII significantly decreased compared to groups I, III, V, and VII, respectively (p<0.05). The TSA treatment had no significant effect on GDF9 expression (Figure 2E p>0.05).

Effect of TSA on the activation of ERK1/2 and on GDF9 protein expression

In previous reports, ERK activity (p-ERK1/2) in cumulus cells was detected at 30 min and maximal levels were observed at 4 h (Su et al., 2002). Hence, we detected ERK activity in cumulus cells that received TSA treatment for either 30 min or 4 h, and we assayed GDF9 expression in the FGOs. As shown in Figure 3A, TSA significantly blocked the activation of ERK1/2 in the cumulus cells (p<0.05). The TSA treatment had no significant effect on GDF9 protein expression (Figure 3B p>0.05).

DISCUSSION

In the present study, we found that TSA treatment inhibited cumulus expansion. Cumulus expansion is a highly coordinated process that occurs a few hours prior to ovulation and involves the production of a complex extracellular matrix (ECM) (Fulop et al., 2003). During COCs in vitro maturation, the oocytes secret one or more factors to promote cumulus granulosa cell proliferation and modulate extracellular matrix components (Vanderhyden et al., 1992). Activation of several key ECM genes in cumulus cells plays crucial roles regulating gonadotropin-dependent cumulus expansion including Has2, Ptgs2 (also known as Cox2), Ptx3, and Tnfaip6 (Fulop et al., 2003; Lim et al., 1997; Su et al., 2003). We determined the expression levels of the ECM genes after TSA treatment and found that TSA significantly reduced the mRNA levels of the cumulus expansion related genes. This phenomenon may result from the TSA-induced blocked activation of ERK1/2. Because the ERK1/2 activity in cumulus cells is essential for gonadotropin-induced cumulus expansion in the mouse. The specific MEK inhibitor U0126 can block GDF9-induced cumulus expansion and suppress the expression of ECM genes (Su et al., 2002). GDF9 is a specific oocyte-secreted factor and a member of the transforming growth factor p (TGFp) superfamily (McPherron et al., 1993; Hayashi et al., 1999). Additionally, TSA can inhibit the expression of tissue inhibitor of metalloproteinases-1 (Timp-1) in the presence of TGFp (Barter et al., 2010), as the metalloproteinases (TIMPs) safeguard ECM integrity by virtue of their ability to inhibit the matrix metalloproteinases (MMPs) (Baker et al., 2002). Hence, another possible reason for the reduction of the mRNAs of ECM genes was that TSA inhibited Timp-1 expression in the presence of TGF[beta], leading to a loss of the ability to safeguard ECM integrity thereby blocking cumulus expansion.

The cumulus-oocyte complexes (COCs) were composed of fully grown oocytes (FGOs) and their surrounding cumulus cells. To determine which components were under the influence of TSA, microsurgical removal of the oocyte from the COC (OOX) was performed following a microsurgical protocol. The FGOs and OOX were pretreated with 100 nM TSA for 30 min or 4 h and were then co-cultured with either OOX or FGOs, respectively, for 15 h. Cumulus expansion was inhibited (Figure 1-VI, VIII), and ECM gene expression was significantly reduced (Figure 2A to D) when the OOX were pretreated with TSA for 30 min or 4 h. ERK1/2 activity in the cumulus cells (Su et al., 2002) and the presence of the specific oocyte-secreted factor GDF9 (Elvin et al., 1999) are essential for cumulus expansion. We further explored the activity of ERK1/2 and GDF9 protein expression and found that TSA significantly blocked the activation of ERK1/2 (Figure 3A, p<0.05). The results were consistent with the previously finding that HDAC inhibitors (TSA) reduce the levels of TGF-[beta]-induced ERK1/2 phosphorylation (p-ERK1/2) (Barter et al., 2010). Hence, in the presence of TGF-[beta], the addition of TSA to the culture medium led to a reduction in p-ERK1/2 levels in the cumulus cells, which most likely inhibited cumulus expansion. The effects of HDAC inhibition on the ERK pathways may be due to enhanced phosphatase activity or reduced activation (Barter et al., 2010). Because recombinant HDAC6 binds directly to the protein phosphatase 1 (PP1) catalytic subunit, TSA disrupts endogenous HDAC6-PP1 complexes and activates PP1 (Brush et al., 2004). TSA treatment had no effect on GDF9 gene and protein expression. Collectively, it seemed that the inhibitory effect of TSA on cumulus expansion was mainly due to its effect on the cumulus cells.

In conclusion, TSA treatment inhibited mouse cumulus cells expansion probably though abolishing ERK1/2 activation and reducing the expressiong of several key ECM genes.

http://dx.doi.org/10.5713/ajas.2013.13128

ACKNOWLEDGEMENTS

This work was supported by the National Natural Science Foundation Project of China (No. 30972102). We thank Dr. Guangbin Zhou, Dr. Qien Yang and NPG language editing for proofreading the manuscript.

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Ming Du, Xiangwei Fu, Yanhua Zhou, and Shien Zhu *

Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture and National Engineering Laboratoryfor Animal Breeding, College of Animal Science and Technology, China Agricultural University, Beijing, China

* Corresponding Author: Shien Zhu. Fax: +86-10-62731767, E-mail: zhushien@cau.edu.cn

Submitted Feb. 28, 2013; Accepted Apr. 8, 2013; Revised Jun. 3, 2013

Table 1. Experimental design

Group           Treatment

I               COC
II              COC+TSA
III             OOX+FGOs
IV              OOX+FGOs+TSA
V               (FGOs+TSA 30 min)+OOX
VI              (OOX+TSA 30 min)+FGOs
VII             (FGOs+TSA 4 h)+OOX
VIII            (OOX+TSA 4 h)+FGOs

Table 2. Primer sequences

Gene symbol    Forward                  Reverse

Has2           CGAGTCTATGAGCAGGAGCTG    GTGATTCCGAGGAGGAGAGACA
Ptgs2          CCCTTCCTCCCGTAGCAGAT     TGAACTCTCTCCGTAGAAGAACCTTT
Ptx3           TTGCTGAGACCTCGGATGAC     GCGAGTTCTCCAGCATGATGA
Tnfaip6        ATACAAGCTCACCTACGCCGA    ATCCATCCAGCAGCACAGACAT
GDF9           GCTCTATAAGACGTATGCTACC   CAGAGTGTATAGCAAGACCGAT
Rpl19          TCAGGCTACAGAAGAGGCTTGC   ATCAGCCCATCCTTGATCAGC
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Author:Du, Ming; Fu, Xiangwei; Zhou, Yanhua; Zhu, Shien
Publication:Asian - Australasian Journal of Animal Sciences
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Geographic Code:9CHIN
Date:Nov 1, 2013
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