|Year : 2014 | Volume
| Issue : 7 | Page : 112-119
Regulation of luteinizing hormone receptor expression by an RNA binding protein: Role of ERK signaling
K.M.J. Menon1, Bindu Menon2
1 Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI, USA
2 Department of Obstetrics and Gynecology, University of Michigan Medical School, Ann Arbor, MI, USA
|Date of Submission||21-Jan-2013|
|Date of Web Publication||10-Feb-2015|
1150 W Medical Center Dr. 6428 Med Sci 1, Ann Arbor, MI-48104
Source of Support: None, Conflict of Interest: None
| Abstract|| |
A specific luteinizing hormone receptor (LHR) mRNA binding protein (LRBP) has been identified and purified. This LH receptor mRNA binding protein selectively binds to the polypyrimidine rich bipartite sequence in the coding region of the LHR mRNA and accelerates its degradation. In response to preovulatory LH surge, the LH receptor expression in the ovary undergoes downregulation by accelerated degradation of LH receptor mRNA through the involvement of this RNA binding protein. Here we describe the intracellular mechanism triggered by LH/hCG (human chorionic gonadotropin) that leads to the regulated degradation of LH receptor mRNA. Downregulation of LH receptor mRNA was induced by treatment of cultured human granulosa cells with 10 IU of hCG. Activation of downstream target, extracellular signal-regulated protein kinase 1 and 2 (ERK 1/2) showed an increase within five min and sustained up to 1 h. Confocal analysis showed that ERK1/2 translocates to the nucleus after 15 min of hCG treatment. This leads to an increase in LRBP expression which then causes downregulation of LH receptor mRNA by accelerating its degradation. Treatment with UO126 or transfection with ERK specific siRNA (small interfering RNA) resulted in the abolishment of ERK activation as well as LHR mRNA downregulation. RNA electrophoretic mobility gel shift assay of the cytosolic fractions showed that hCG-induced increase in the LH receptor mRNA binding activity was also abrogated by these treatments. These results show that LH/hCG-induced LH receptor mRNA downregulation is initiated by the activation of ERK1/2 pathway by regulating the expression and activity of LH receptor mRNA binding activity.
Keywords: ERK1/2 - Human chorionic gonadotropin - luteinizing hormone receptor - mRNA-binding protein - post transcriptional regulation
|How to cite this article:|
Menon K, Menon B. Regulation of luteinizing hormone receptor expression by an RNA binding protein: Role of ERK signaling. Indian J Med Res 2014;140, Suppl S1:112-9
|How to cite this URL:|
Menon K, Menon B. Regulation of luteinizing hormone receptor expression by an RNA binding protein: Role of ERK signaling. Indian J Med Res [serial online] 2014 [cited 2020 Aug 11];140, Suppl S1:112-9. Available from: http://www.ijmr.org.in/text.asp?2014/140/7/112/151119
The LH/hCG (luteinizing hormone/human chorionic gonadotropin) receptor (LHR) expressed in the gonads regulates the ovarian and testicular function ,, . Although gonadal tissues are the primary sites of its expression, it is now well-established that LHR is also expressed in many non-gonadal tissues  . LHR along with follicle stimulating hormone (FSH) receptor and thyroid stimulating hormone (TSH) receptor belongs to the family of rhodopsin/β2 adrenergic receptor subfamily of G protein coupled receptors  . Binding of the LH or hCG to the extracellular domain of LHR causes a conformational change leading to guanosine di-and triphosphate (GDP-GTP) exchange on the cognate G protein. This results in the dissociation of the inhibitory beta-gamma subunit from the alpha subunit leading to the activation of adenylatecyclase to increase the intracellular concentration of adenosine cyclic 3', 5' cyclic monophosphate (cAMP). Cyclic AMP then activates protein kinase cascade and activates multiple signaling pathways culminating in increased steroidogenesis and stimulation of other cellular functions. It has been shown that at higher concentrations, LH or hCG can also activate phospholipase C resulting in the formation of inositoltriphosphate (IP 3 ) and diacylglycerol (DAG) ,, . The physiological significance of this pathway in LH-regulated ovarian function is not clearly understood.
LHR is expressed in the follicles, theca cells and corpus luteum of the ovary and the expression pattern shows considerable changes throughout ovarian cycle ,, . In growing follicles, LHR expression is regulated by the combined actions of FSH and estradiol. Consequently, the expression of LHR increases during follicular growth as it acquires the ability to secrete estrogens  . The receptor expression is transiently downregulated in response to pre-ovulatory LH surge, which then recovers from down-regulation after 72 h reaching maximum level by the mid luteal phase ,,, . The LHR level falls off as the corpus luteum undergoes regression. The molecular mechanism underlying the regulation of LHR expression has been investigated in depth in our laboratory. Using rodent and human ovarian models, we have determined that the regulation of LHR occurs through post-transcriptional mechanisms mediated by a specific LHR mRNA binding protein , . This article will focus on the signaling pathways involved in the post-transcriptional regulation of LHR expression.
The downregulation of LHR occurs in response to preovulatory LH surge or in response to the administration of a pharmacological dose of LH or hCG. The loss of the ligand binding activity is closely coupled to the loss of the steady state levels of LHR mRNA. In human, this phenomenon occurs during ovulation induction by the administration of hCG prior to ovum retrieval for in vitro fertilization  . Granulosa cells isolated from the retrieval fluids showed complete loss of LHR mRNA on the day of retrieval, when examined by Northern blot analysis ([Figure 1])  . The granulosa cells were then cultured for different periods of time and RNA was extracted from the harvested cells for examination of the reappearance of LHR mRNA. The recovery from down regulation began approximately 48 h later and reached maximum level by day 4 in culture ([Figure 1]). This phenomenon can be demonstrated in a pseudopregnant rat model by treatment with a single dose of 50 IU of hCG to down regulate LHR. The loss of LHR mRNA transcripts during down regulation is shown in [Figure 2]A  . The left hand panel shows the expression of LHR mRNA transcripts in the saline treated control ovaries. The expression of LHR mRNA transcripts in response to the administration of hCG that mimics preovulatory LH surge is shown on the right hand panel. The LHR mRNA expression remains suppressed up to 48 hours and recovers from downregulation by 72 h , . The loss of receptor mRNA could be either due to a decrease in the rate of synthesis or due to increased degradation. To examine these possibilities, nuclear run-on assays were performed to determine the transcription rate during hCG-induced LHR downregulation  . The results showed that the transcription rate remained identical in both control and hCG treated groups suggesting that the loss of the steady state levels of LHR mRNA is not due to decreased transcription, but rather resulted from increased degradation  . Furthermore, the half-life of LHR mRNA was significantly reduced in the hCG treated group when compared to the mRNA decay rate of the control group ([Figure 2]B). There was approximately a three-fold decrease in mRNA half-life in the down- regulated group.
The steady state level of mRNA, in general, is controlled by the rate of its synthesis and the rate of degradation. It is now clear that highly regulated mRNAs are controlled, at least in part, by modulating their degradation. In the majority of instances of post-transcriptional regulation of mRNA, the changes in the stability of mRNA appear to result from changes in the binding of cytoplasmic proteins, known as trans factors, to defined sequences or structures, known as cis elements, in the target mRNA, forming a ribonucleoprotein complex. These trans factors can either increase or decrease the stability of RNA. t0 he binding of proteins to mRNAs can occur either on 3' end, 5' end or on the coding sequence ,,,,,, . On the basis of these facts, the possible existence of an LHR mRNA binding protein was examined in the cytosolic fractions from the ovaries after injection with a dose of hCG that is known to downregulate LHR mRNA expression.
Identification of LHR mRNA binding protein
Our first attempt was to examine whether a specific LHR mRNA binding protein participates in LH/hCG regulated downregulation of LHR mRNA expression. Cytosolic fractions from control and downregulated ovaries were prepared and the ability of these fractions to bind LHR mRNA was examined by performing RNA electrophoretic mobility shift assay (REMSA)  . A 100,000 x g supernatant (S100) fraction of the ovarian homogenate was incubated with [ 32 P] labelled LHR mRNA that was prepared by transcribing the full length cDNA encoding the LHR in the presence of [α 32 P] UTP. After treatment with RNAses to degrade unreacted [ 32 P] labelled RNA, the ribonucleoprotein complex was subjected to electrophoresis under non-denaturing conditions, and autoradiography. We compared the ability of the S100 fractions from the control and hCG downregulated ovaries to bind radiolabelled LHR mRNA. The results showed that there were two prominent bands designated as LRBP-1 and LRBP-2 (LHR binding protein), corresponding to molecular weight 50 and 45 kDa, respectively, in both the control and down regulated ovaries  . The intensity of LRBP-1 was 3-fold higher in the downregulated group compared to the saline treated control. No significant change in the intensity in LRBP-2 was noticed. Since the hormonal induction of LRBP-1 was significantly higher, we focused our attention only on LRBP-1.
Studies were carried out to determine the nucleotide sequence involved in the interaction of LHR mRNA with proteins in the S100 fraction. Truncated segments of the full length LHR mRNA were incubated with ovarian S-100 fractions and electrophoretic mobility shift assays were performed to localize the region of LHR mRNA that interacted with the protein. The results of these studies coupled with the results from RNA hydroxyl radical foot- printing revealed that the contact site of the interaction of LRBP-1 with LHR mRNA consisted of a bipartite polypyrimidine- rich sequence corresponding to the nucleotides 203-220 located in the region encoding the amino terminus of LHR  .
After establishing the existence of an inducible RNA binding protein that recognizes a specific structure of the LHR mRNA, we examined the LHR mRNA binding activity under conditions that mimic follicle maturation and the LH surge  . Since the expression of the LHR is increased during follicle maturation and, conversely, the LHR expression is decreased during downregulation, these two paradigms were selected to examine whether changes in LHR expression have any bearing on the LHR mRNA binding activity. In response to treatment of 23 day old rats with pregnant mare's serum gonadotropin (PMSG), as expected, there was an increase in the expression of LHR mRNA by 56 h due to the induction of LHR mRNA by the FSH type of activity associated with pregnant mare's serum gonadotropin (PMSG). Fifty six hours after PMSG treatment, administration of 50 IU of hCG caused a transient decrease in LHR mRNA expression during the ensuing 24 h period as a result of downregulation. The LHR mRNA level returned to the hCG pretreatment level by 72 h. Thus, the changes in LHR mRNA were consistent with the expected up- and downregulation following the treatments. The LHR mRNA binding activity showed a strikingly different pattern in response to these treatments. When the expression of LHR mRNA was high in response to PMSG treatment, the LRBP activity showed a decrease. Conversely, an increased expression of LHR mRNA binding activity was seen when LHR mRNA expression was low in response to LHR downregulation  . Thus, there appeared to be an inverse relationship between the expression of LHR mRNA binding activity and LHR mRNA expression. These results have clearly pointed out that LRBP is a regulator of LHR mRNA expression.
Signaling mechanism involved in LRBP-mediated LHR mRNA degradation
The cellular mechanism that triggers the LRBP expression in response to LH/hCG treatment that leads to LHR mRNA downregulation was examined using cultured human granulosa cells. Specifically, the participation of protein kinase A (PKA) and ERK signaling pathways, the two downstream signaling molecules involved in LH action was examined during hCG- induced downregulation of LHR expression. First, we examined the possible participation of PKA in this process by blocking PKA activity by pretreatment with 10 micromolar concentrations of a pharmacological inhibitor, H89 prior to treatment with 10 IU of hCG for 12 h to down regulate LH receptor. The effect of blockade of PKA by H89 on the downregulation of LHR and induction of LRBP were determined by performing real time PCR. The results showed that, as expected, treatment with hCG, resulted in downregulation of LHR mRNA ([Figure 3]A)  . This down-regulation was abolished when cells were preincubated with H89 prior to hCG addition. These results showed that the hCG-induced activation of PKA is required for inducing downregulation of LHR  .
Since LH/hCG- induced LHR mRNA downregulation is mediated by LRBP ,,, , the effect of preincubation with H89 on the expression of LRBP was examined  . The results showed that while treatment with hCG alone caused an increase in LRBP expression ([Figure 3]B), more importantly, treatment with H89 prior to hCG treatment caused a significant reduction in the expression of LRBP. From these results, we concluded that abolition of hCG-induced PKA activation abrogated both LRBP expression and downregulation of LHR mRNA.
It has been shown that ERK is downstream of PKA in G protein-coupled receptor (GPCR) mediated signaling pathways ,,, . To demonstrate that this is also true in human granulosa cells, the sensitivity of H89 on ERK1/2 activation in response to hCG was examined. Treatment of granulosa cells with hCG markedly increased the phosphorylation of ERK1/2 in a time dependent manner, starting as early as 5 min and lasting upto 30 min, but decreased to control levels by 1 h ([Figure 4]A)  . Pretreatment with the PKA inhibitor, H89 blocked this increase clearly showing that ERK1/2 is downstream of PKA in human granulosa cells (Fig 4B).Therefore, the involvement of ERK1/2 in hCG-mediated downregulation of LHR mRNA, the effect of blocking ERK activation on LHR downregulation and LRBP expression were examined by depleting ERK using siRNA technique. First, the effectiveness of ERK specific siRNA to suppress ERK expression was assessed by incubating human granulosa cells with ERK-specific siRNA for 48 h. The results showed that ERK specific siRNA was effective in significantly reducing ERK expression while a non-specific siRNA produced no change in ERK level ([Figure 5]A)  . After establishing the effectiveness of ERK specific siRNA to block ERK expression, the effect of ERK depletion on LHR mRNA downregulation was examined. Human granulosa cells were exposed to ERK-specific siRNA for 48 h to knockdown ERK expression and the ability of hCG to downregulate LH receptor was tested by incubating with 10 IU of hCG for 12 h. The results showed that while hCG alone caused downregulation of LHR, this downregulation by hCG was not seen in cells pretreated with ERK specific siRNA ([Figure 5]B). Furthermore, hCG-induced LRBP expression and activity were also significantly reduced in cells where ERK expression was knocked down by siRNA compared to controls treated with a non-specific siRNA ([Figure 5]C and D).These results clearly demonstrated that LH-mediated ERK activation is required for LHR downregulation and that this response is mediated by LRBP  .
| Conclusion|| |
In summary, based on the present and ongoing studies, we propose a model for the mechanism for LH/hCG-mediated downregulation of LHR mRNA expression, as depicted in [Figure 6]  . In response to preovulatory LH surge or in response to hCG administration to induce ovulation, the initial interaction of LH with its receptor results in increased cyclic AMP production. This increase leads to activation of PKA and ERK signaling cascade to increase LRBP expression. LRBP in turn binds LHR mRNA and forms an untranslatable ribonucleoprotein complex and targets LHR mRNA for degradation in P bodies. Thus, accelerated degradation results in the transient loss of LH receptor. This loss of LH receptor causes a temporary halt in the LH/hCG-mediated signaling during the differentiation of granulosa cells to luteal cells. Thus, LH signaling through PKA and ERK1/2 pathway is required for LHR down regulation in response to preovulatory LH surge or in response to hCG treatment for ovulation induction.
| Acknowledgment|| |
The studies were supported by the United States Public Health Service grant, NIH HD R37 06656 to the first author (KMJM). Authors thank the Endocrine Society and the American Society of Biological Chemistry and Molecular Biology for granting us permission to reproduce figures from our previous publications.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]