Activities of Amphioxus GH-Like Protein in Osmoregulation: Insight into Origin of Vertebrate GH Family

Li, Mengyang; Jiang, Chengyan; Zhang, Yu; Zhang, Shicui

doi:https://doi.org/10.1155/2017/9538685

International Journal of Endocrinology

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Abstract Introduction Materials and Methods Results Discussion Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2017 | Article ID 9538685 | https://doi.org/10.1155/2017/9538685

Activities of Amphioxus GH-Like Protein in Osmoregulation: Insight into Origin of Vertebrate GH Family

Mengyang Li,^1,2Chengyan Jiang,^1,3Yu Zhang ,¹and Shicui Zhang¹

Academic Editor: Alexander Schreiber

Received04 Oct 2016

Accepted14 Nov 2016

Published19 Mar 2017

Abstract

GH is known to play an important role in both growth promotion and osmoregulation in vertebrates. We have shown that amphioxus possesses a single GH-like hormone (GHl) gene encoding a functional protein capable of promoting growth. However, if GHl can mediate osmoregulation remains open. Here, we demonstrated clearly that GHl increased not only the survival rate of amphioxus but also the muscle moisture under high salinity. Moreover, GHl induced the expression of both the ion transporter Na⁺-K⁺-ATPase (NKA) and Na⁺-K⁺-2Cl⁻ cotransporter (NKCC) in the gill as well as the mediator of GH action IGFl in the hepatic caecum, indicating that GHl fulfills this osmoregulatory activity through the same mechanisms of vertebrate GH. These results together suggest that the osmoregulatory activities of GH had emerged in the basal chordate amphioxus. We also proposed a new model depicting the origin of pituitary hormone family in vertebrates.

1. Introduction

Growth hormone (GH) and prolactin (PRL) are structurally related pituitary polypeptide hormones that belong to a superfamily of helical cytokines. Both GH and PRL act by interacting with single transmembrane domain receptors that are also structurally related and belong to the type 1 cytokine receptor superfamily [1, 2]. These hormones and their receptors are believed to have evolved from common ancestral genes through gene duplication and subsequent divergence early in vertebrate evolution [3, 4]. However, questions remain about the timing and subsequent elaboration of gene duplication and the elucidation of genetic innovations that may have contributed to the origin and subsequent divergence of pituitary hormones and their receptors in modern vertebrates.

GH and PRL are both multifunctional and share some overlapping biological properties [4, 5]. For example, they are both known to be involved in the regulation of hydromineral balance in fishes [6, 7]. GH has been shown to facilitate seawater (SW) adaptation in several fishes including salmonids, tilapia, and killifish [8–11], while PRL shown to be an important freshwater- (FW-) adapting hormone regulating FW adaptation in tilapia and killifish [12, 13]. GH has been reported to be able to induce the production of ion transporter Na⁺-K⁺-ATPase (NKA) [11, 14, 15] and Na⁺-K⁺-2Cl⁻ cotransporter (NKCC) [16] that provide the driving force for ion-transporting functions of chloride cells in the gills [17–19]. In addition, insulin-like growth factor-I (IGF-I), which mediates many growth-promoting actions of GH, also appears to mediate the osmoregulatory activity of GH during SW acclimation in salmonids [20, 21]. By contrast, PRL usually maintains plasma homeostasis of fishes in FW by altering salt and water permeability across epithelial cell membranes in the gill, gut, and kidney [22–25].

Amphioxus or lancelet belongs to the subphylum Cephalochordata, an extant representative of the most basal chordates. Recently, we have found that amphioxus possesses a single GH-like hormone (GHl) gene encoding a functional protein capable of promoting growth [26]. Moreover, the animal also has a homologue GH/PRLlBP of vertebrate GH-binding protein (GHBP), which is a soluble and truncated form of GHR lacking transmembrane and intercellular parts [26]. However, does GHl, like vertebrate GH, play a role in osmoregulation? And if so, how does it function in amphioxus? The aim of this study is therefore to answer these questions.

2. Materials and Methods

2.1. General Experimental Design

In this study, we first injected the amphioxus with recombinant GHl to test if GHl plays an osmoregulatory role as vertebrate GH does. We then explored the osmoregulatory mechanism of GHl. Finally, we investigated if a vertebrate-like GH/IGF axis is also involved in the osmoregulation of amphioxus by examining the correlation of salinity and expression of GHl/IGFl axis genes.

2.2. Animals

Animal experiments were approved by the Ethics Committee of the Laboratory Animal Administration of Shandong Province (permission number SD2007695). All the experiments were performed in accordance with relevant guidelines and regulations. Amphioxus Branchiostoma japonicum with average body length of about 2 cm were collected from the seashore in Qingdao city, Shandong province, China. They were fed and cultured as described by Wang and Zhang [27].

2.3. Recombinant Proteins

The recombinant protein of amphioxus GHl (rGHl) was prepared as described by Li et al. [26]. Zebrafish recombinant GH (rzGH) was purchased from ProSpec (East Brunswick, NJ, USA). The recombinant protein of zebrafish PRL (rzPRL) was produced by the methods of Li et al. [26]. Briefly, the cDNA encoding mature PRL (25 to 210 amino acids) was amplified by PCR, and the PCR products were digested with EcorI and XhoI and subcloned into the plasmid expression vector pET28a (Novagen, Germany) cut with the same restriction enzymes. The plasmid constructed was verified by sequencing and transformed into the cells of Escherichia coli BL21 (DE3). The recombinant protein was expressed, purified, and refolded as described by Li et al. [26]. The purified protein was analyzed on a 12% SDS-PAGE gel and immunostained using anti-His-tag monoclonal antibody (CWBIO, China) as the primary antibody. All the protein concentrations were determined with BCA protein assay kit (Beyotime, China).

2.4. Salinity Tolerance Assay

Salinity tolerance assay was performed to explore if amphioxus GHl, like fish GH or PRL, plays an osmoregulatory role. Pilot experiments showed that when amphioxus was administered with 10 μl of saline (0.9% NaCl) by intracoelomic injection and cultured in seawater with 38‰ or 15‰ salinity, 80% to 100% mortality was observed at 96 h after injection (data not shown). Therefore, these salinities were chosen for the following experiments. Amphioxi were first acclimated to 30‰ seawater, and then, 20 animals per group were each injected with either 10 μl of saline or 10 μl saline containing 10 ng rGHl or 10 ng rzGH or 10 ng rzPRL. The dosages used were according to the previous studies in fishes [14, 16, 28]. Soon after injection, the animals were cultured in 500 ml of seawater with 38‰ or 15‰ salinity at ambient photoperiod and at room temperature. The salinity was prepared by mixing Millipore ultrapure water with artificial sea salt (Haijia, China). The seawater was changed every 24 h, and the mortality was checked simultaneously. The beating of velar tentacles on the velum can be used as “living marker” of amphioxus; if the tentacles stopped beating, even in response to pricking, then the animals were believed to be “dead.”

2.5. Cloning and Expression of nka and nkcc

Na⁺-K⁺-ATPase (NKA) and Na⁺-K⁺-2Cl⁻ cotransporter (NKCC) located in the basolateral membrane of the chloride cells in the gill of fishes are accepted as the major ion transporters [17–19]. Our searching of B. floridae genome database (http://genome.jgi-psf.org//Brafl1/Brafl1.home.html) for the homologues of vertebrate NKA and NKCC (using NKA alpha 1 and NKCC1 as queries) revealed the presence of a single NKA (GenBank accession number: XP_002610679.1) and NKCC (GenBank accession number: XP_002609755.1), respectively. We then set to clone nka and nkcc from B. japonicum. Total RNAs were extracted with Trizol (TaKaRa, Dalian, China) from B. japonicum and digested with RNase-free DNase to eliminate the genomic contamination. The first-strand cDNA was synthesized with reverse transcription system using oligo d(T) primer. To amplify the fragments of nka and nkcc cDNAs, polymerase chain reaction (PCR) was performed using the first-strand cDNA as template, in a total volume of 20 μl PCR reaction mixture containing 1 × PCR buffer, 0.5 unit of EX Taq DNA polymerase, and 0.4 μM of the gene-specific primers P5 and P6 as well as P9 and P10 (Table 1), which were designed on the basis of the putative nka and nkcc sequences found in B. floridae genome database. PCR was carried out at 94°C for 5 min, followed by 34 cycles at 94°C for 30 s, 54°C for 30 s, 72°C for 1 min, and a final extension step at 72°C for 7 min. The PCR products were gel-purified using DNA gel extraction kit (Axygen, Union City, USA), ligated into the T/A cloning vector pGEM-T easy (Promega, Shanghai, China) at 4°C overnight, and transformed into the competent cells of E. coli (Tiangen, Beijing, China). The positive clones were selected and sequenced with ABI PRISM 3730 DNA sequencer. The sequences were searched in GenBank with BLASTx for comparative analysis. Sequence comparison against NKA and NKCC was performed by the MegAlign program of the LASERGENE software suit (DNASTAR). Protein domains were analyzed using the SMART program (http://smart.embl-heidelberg.de/).

To examine the expression profiles of nka and nkcc, whole amphioxus and the different tissues including the gill, hindgut, hepatic caecum, notochord, muscle, and skin dissected out of amphioxus were homogenized in Trizol Reagent (Invitrogen) and stored at −80°C until use. Total RNAs extraction and the first-strand cDNA synthesis were performed as above. Semiquantitative RT-PCR (qRT-PCR) was performed using quantified cDNA templates (about 0.3 to 0.4 μg/μl) and the primers on ABI 7500 real-time PCR system (Applied Biosystems, USA). The PCR primers specific of nka (P7 and P8), nkcc (P11 and P12), and ef1a (P13 and P14) were designed using premier 5.0 program [29]. The ef1a gene was chosen as the reference for internal standardization. SYBR Premix ExTaq™ (Takara, Japan) was used according to the manufacturer’s protocol with a primer concentration of 200 nM. The reaction conditions were as follows: 95°C for 1 min, followed by 40 cycles of 95°C for 5 s, 60°C for 15 s, and 72°C for 35 s. Dissociation analysis was performed at the end of each PCR reaction to confirm the amplification specificity. After the PCR program, the data were analyzed with ABI 7500 SDS software (Applied Biosystems) and quantified with the comparative Ct method (2^–ΔΔCt) based on Ct values for genes and the reference ef1a in order to calculate the relative mRNA expression level.

2.6. Assay for Effects of Salinity on Gene Expression and Muscle Moisture

A total of 60 amphioxi was acclimated in the seawater with 25‰ salinity for 15 days and then divided into 2 groups: 30 animals were transferred to seawater with 30‰ salinity, and 30 still maintained in seawater with 25‰ salinity. Ten animals were then sampled from each group at 0, 48, and 72 h after transferring to seawater, and the Hatschek’s pit, gill, and hepatic caecum were dissected out of the animals and homogenized in Trizol. The preparation of total RNAs and the expression of both nka and nkcc in the gill and ghl in the Hatschek’s pit and gill as well as gh/prllbp and igfl in the hepatic caecum and gill were performed as described above. The collection of the Hatschek’s pit was carried out as described by Fang and Wang [30]. The wheel organ on the right side of the notochord was the part with Hatschek’s pit and was dissected out under microscope. The PCR primers specific of nka (P7 and P8) and nkcc (P11 and P12) were as above, and the primers specific of gh/prllbp (P15 and P16), igfl (P17 and P18), and ghl (P19 and P20) were designed using premier 5.0 program.

The muscle was also dissected out of the animals sampled. The tissue was cut into pieces 1 mm³, dried on filter paper, and soon transferred to 1.5 ml Eppendorf tubes. The muscle moisture was measured as described by Mccormick [28] and Breves et al. [31]. Briefly, 100 mg of the muscle from each group was dried to a constant weight at 60°C, and the water content was then measured gravimetrically.

2.7. Assay for Effects of rGHl and rzGH on Gene Expression In Vitro

The gill and hepatic caecum were dissected out of amphioxus, cut into pieces (~1 mm³), and cultured in MEM medium containing 2.2 mg/ml NaHCO₃, 100 IU/ml penicillin, 100 μg/ml streptomycin, and different concentrations of rGHl or rzGH (0, 10, 100, and 1000 ng/ml) at 25°C. After 4 h culture, the tissue pieces of the gill and hepatic caecum were pooled and homogenized immediately in Trizol Reagent, and total RNAs were prepared. The expressions of nka and nkcc in the gill as well as gh/prllbp and igfl in the gill and hepatic caecum were analyzed by qRT-PCR as above.

2.8. Assay for Effects of rGHl and rzGH on Gene Expression In Vivo

A total of 90 amphioxi was divided into 3 groups (30/group), and each animal was injected with either 10 μl of saline or 10 μl saline plus 10 ng rGHl or 10 ng rzGH. They were then cultured in 500 ml natural seawater and fed once a day with the single-cell alga Spirulina sp. Ten amphioxi were sampled from each group at 0, 24, and 48 h after injection, respectively, and the gill and hepatic caecum were dissected out of the animals. Both the tissues were homogenized in Trizol, and total RNAs were prepared. The expressions of nka and nkcc in the gill as well as gh/prllbp and igfl in the gill and hepatic caecum were analyzed by qRT-PCR as above.

2.9. Assay for Effects of rGHl and rzGH on NKA Activity and Muscle Moisture

A total of 90 amphioxi was divided into 3 groups (30/group), and each animal was injected with either 10 μl of saline or 10 μl saline plus 10 ng rGHl or 10 ng rzGH. They were cultured and sampled as above. Both the gill and muscle were dissected out of the animals sampled. The tissues were cut into pieces 1 mm³, dried on filter paper, and soon transferred to precooled 1.5 ml Eppendorf tubes. The NKA activity in the gill (ca. 50 mg per group) was analyzed with NKA activity kit (Solarbio, Beijing) as described as Zeng et al. [32]. One unit of enzymatic activity was defined as 1 μmole ADP released per hour. The muscle moisture was measured as described above.

2.10. Statistical Analysis

Salinity tolerance experiment was repeated twice, while all the other experiments were performed in triplicate and repeated three times. The survival curve was generated by GraphPad Prism 5. The data of the experiments of effects of salinity on gene expression and muscle moisture were analyzed by two-way ANOVA, while the other data analyzed by one-way ANOVA. The difference at was considered significant. All the data were expressed as mean ± SEM.

3. Results

3.1. rGHl Enhances Salinity Tolerance of Amphioxus

Recombinant amphioxus GH-like protein rGHl was expressed and purified as described by Li et al. [26]. Recombinant zebrafish prolactin rzPRL with His tag was expressed in E. coli and purified by chromatography on a Ni-NTA resin column. rzPRL was subjected to SDS-PAGE, which yielded a single band corresponding to the expected sizes of ~24.6 kDa. Western blotting revealed that rzPRL reacted with rabbit anti-His-tag antibody, indicating that rzPRL was correctly expressed (see Supplementary Figure in Supplementary Material available online at https://doi.org/10.1155/2017/9538685).

Figure 1 shows the survival rates of amphioxus injected with saline, rGHl, rzGH, or rzPRL, followed by culture in seawater with different salinity. The culture under high salinity (38‰) resulted in 52.5%, 82.5%, and 100% as well as 50%, 75% and 100% cumulative mortality, respectively, in the saline- and rzPRL-injected amphioxus at 72, 96, and 120 h after injection. The mortalities of these two groups were not statistically different. The same culture caused only 37.5%, 48.5%, and 67.5% as well as 22.5%, 52.5%, and 65% cumulative mortality, separately, in the rGHl- and rzGH-injected animals at the same experimental periods. The survival rates of the rGHl- and rzGH-injected groups were significantly higher than control (Figure 1(a)). By contrast, the culture under low salinity (15‰) resulted in 40% and 80%, 60% and 100%, and 47.5% and 87.5% as well as 50% and 85% cumulative mortality, individually, in the saline-, rGHl-, rzGH-, and rzPRL-injected animals at 72 and 96 h after injection, and none of the animals survived by 120 h. No statistical difference was observed in the groups (Figure 1(b)). These data together indicated that amphioxus GHl, like zebrafish GH, could promote salinity tolerance of amphioxus, but zebrafish PRL could not.

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3.2. rGHl Induces Expression of nka and nkcc

Partial cloning revealed the presence of nka and nkcc in amphioxus that are highly identical to their counterparts in fish and mammalian species. Specifically, the nka cDNA fragment (GenBank accession number: KU312041) we cloned from B. japonicum was 629 bp long, encoding a deduced peptide of 209 amino acids which has 78.9% to 80.4% identity with vertebrate NKA3, and a cation_ATPase domain characteristic of NKA, and the nkcc cDNA fragment (GenBank accession number: KU312042) obtained was 960 bp long, coding for a deduced NKCC-like peptide of 319 amino acids, which possesses 45.8% to 48.3% identity with vertebrate NKCC1, and both AA_permease and SLC12 domains typical of NKCC (Supplementary Figures and ). As shown in Figures 2(a) and 2(b), both nka and nkcc displayed a tissue-specific expression, with relatively abundant levels in the gill. The gene nkcc was also abundantly expressed in the notochord. To test if salinity change affects the expression of nka and nkcc in the gill, the 25‰ salinity-acclimated animals were transferred to seawater with 30‰ salinity, and the expression of nka and nkcc in the gill was analyzed. No dead animals were observed. As shown in Figures 2(c) and 2(d), the transfer of 25‰ salinity-acclimated amphioxus to seawater with 30‰ salinity resulted in a significant upregulation of nka and nkcc in the gill. Compared with that of 25‰ group, the expression of nka in the gill of 30‰ group was increased to approximately 1.9-fold at 48 and 72 h after transfer. Similarly, compared with that of 25‰ group, the expression of nkcc in the gill of 30‰ group was increased to about 1.8-fold and 5.7-fold, respectively, at 48 and at 72 h after transfer. These suggested that NKA and NKCC were involved in the process of osmoregulation in the gill of amphioxus.

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Figure 2

Identification of nka and nkcc. (a) The expression profiles of nka in the different tissues including the gill, hindgut, hepatic caecum, skin, notochord, and muscle. (b) The expression profiles of nkcc in the different tissues. (c) Expression of nka in the gill of amphioxus cultured under 25‰ or 30‰ salinity. (d) Expression of nkcc in the gill of amphioxus cultured under 25‰ or 30‰ salinity. The ef1α was chosen as internal control for normalization. Data were from 3 independent experiments and expressed as mean ± SEM. The symbol shows .

Next, we tested if rGHl can stimulate the expression of nka and nkcc in amphioxus gill. qRT-PCR showed that both rGHl and rzGH were capable of inducing an upregulation of nka and nkcc in a dose-dependent manner in the gill cultures. The expression of nka in the gill cultures was increased to about 1.8-fold after treatment with 1000 ng/ml rGHl (compared with control; the same below); similarly, the expression of the same gene in the gill cultures increased to about 1.4-fold after treatment with 1000 ng/ml rzGH. Moreover, the expression of nkcc in the gill cultures was increased to about 3.7-fold and 2.0-fold, respectively, after treatment with 100 and 1000 ng/ml rGHl, and its expression in the gill cultures was increased to about 1.7-fold and 4.4 fold, respectively, after treatment with 100 and 1000 ng/ml rzGH (Figures 3(a) and 3(b)). These indicated that GHl acted on the gill directly in a dose-dependent fashion in vitro for the first time, with 100 ng/ml concentration of rGHl being most effective in triggering the expression of nka and nkcc. Interestingly, incubation with 1000 ng/ml rGHl resulted in lowered expression of the genes. rzGH also displayed similar trend as rGHl. The reason for this trend is not clear at present. Possibly, it may be due to the failure of GHR dimerization caused by higher dose of rGHl or rzGH [33].

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Figure 3

Induction of nka and nkcc expressions by rGHl. (a) Expression of nka in the gill cultures in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (b) Expression of nkcc in the gill cultures in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (c) Expression of nka in the gill of amphioxus injected with saline, rGHl, or rzGH. (d) Expression of nkcc in the gill of amphioxus injected with saline, rGHl, or rzGH. (e) NKA activity in the gill of amphioxus injected with saline, rGHl, or rzGH. One unit of enzymatic activity was defined as 1 μmoles ADP released per hour. Data were from 3 independent experiments and expressed as mean ± SEM. The symbol shows .

Injection of rGHl or rzGH into amphioxus also induced an increased expression of nka and nkcc in the gill in vivo. Compared with control group within the same time (the same below), the expression levels of nka in the gill were upregulated about 1.5-fold and 2.0-fold at 24 and 48 h after injection of rGHl, and the expression levels of the same gene upregulated about 1.3-fold and 1.8-fold at 24 and 48 h after injection of rzGH. Similarly, the expression of nkcc in the gill was about 1.8-fold higher than that of control at 48 h after injection of rGHl, and the expression of nkcc in the same tissue was about 1.9-fold higher than that of control at 48 h after injection of rzGH (Figures 3(c) and 3(d)). In addition, enzymatic activity assay revealed that injection of rGHl or rzGH into amphioxus triggered an increase in NKA activity in the gill at 24 to 48 h, consistent with the results of nka expression. The gill NKA activity in the gill of control group was 5.098 U/mg, 4.951 U/mg, and 5.363 U/mg, respectively, at 0 h, 24 h, and 48 h after injection. By contrast, the NKA activity in the gill of rGHl group was 5.028 U/mg, 6.304 U/mg, and 6.486 U/mg, individually, at 0 h, 24 h, and 48 h after injection, and the NKA activity in the gill of rzGH group was 5.044 U/mg, 5.259 U/mg, and 5.638 U/mg, separately, at 0 h, 24 h, and 48 h after injection (Figure 3(e)). Several studies have shown that injection of vertebrate GH induced about 1.5-fold to 2-fold increase in the NKA and NKCC in fish gill [11, 16, 28]. We demonstrated that amphioxus GHl, like vertebrate GH, was able to induce the expression of nka and nkcc in the gill in vivo. Besides, the trends of changes in the NKA activity and nka expression patterns affected by rGHl were both similar to that of rzGH. These showed that amphioxus GHl as well as zebrafish GH had a similar capacity to stimulate the expression of nka and nkcc, suggesting that GHl was able to mediate the salinity tolerance in amphioxus.

3.3. rGHl Increases Muscle Moisture

Muscle usually loses moisture under high salinity environment. Thus, the relationship between salinity change and muscle moisture was tested. When the 25‰ salinity-acclimated animals were transferred to seawater with 30‰ salinity, their muscle moisture was 83.1% and 83.6% at 48 and 72 h after the transfer (Figure 4(a)), respectively. It is clear that the muscle moisture of the animals transferred to 30‰ salinity was significantly lower than that of 25‰ salinity-acclimated animals at 48 h after transfer. This indicated that higher salinity could reduce the muscle moisture of amphioxus in a short term.

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Next, we tested the effect of rGHl on muscle moisture. When the animals cultured under 30‰ salinity were injected with saline, their muscle moisture was 83.4% and 84.8% at 24 and 48 h after injection (Figure 4(b)), respectively. By contrast, when the same animals were injected with saline plus rGHl or rzGH, their muscle moisture was increased to 83.7% and 86.0% as well as 83.5% and 85.1% at 24 and 48 h after injection (Figure 4(b)), individually. These indicated that rGHl as well as rzGH could increase the muscle moisture of amphioxus, providing an additional evidence that GHl was a regulator of salinity tolerance.

3.4. rGHl Induces Expression of gh/prllbp

Sohm et al. [34] and Einarsdóttir et al. [35] both showed that GHBP was upregulated by GH and higher salinity in fish. To test if the GH/PRLlBP is associated with salinity tolerance of amphioxus, we examined the effects of rGHl and rzGH on the expression of gh/prllbp in the hepatic caecum and gill. As shown in Figures 5(a) and 5(b), both rGHl and rzGH clearly induced the expression of gh/prllbp in the tissue cultures of gill and hepatic caecum in a dose-dependent fashion (compared with control) which was similar to the results obtained by Sohm et al. [34] and Einarsdóttir et al. [35]. Similarly, injection of rGHl and rzGH stimulated the expression of gh/prllbp in the gill and hepatic caecum; and this increase in gh/prlllbp expression (Figures 5(c) and 5(d); compared with the control within the same time) was always related to higher concentration of rGHl or rzGH. These suggested that amphioxus GHl as well as zebrafish GH both could upregulate the expression of gh/prllbp in the gill and hepatic caecum, thereby contributing to salinity tolerance.

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Figure 5

Induction of gh/prllbp expression by rGHl. (a) Expression of gh/prllbp in the cultures of the hepatic caecum in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (b) Expression of gh/prllbp in the cultures of the gill in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (c) Expression of gh/prllbp in the hepatic caecum of amphioxus injected with saline, rGHl, or rzGH. (d) Expression of gh/prllbp in the gill of amphioxus injected with saline, rGHl, or rzGH. Data were from 3 independent experiments and expressed as mean ± SEM. The symbol shows .

3.5. rGHl Induces Expression of igfl

GHl was shown to be able to regulate growth through IGF action; thus, we tested the effects of rGHl and rzGH on the expression of igfl in the hepatic caecum and gill of amphioxus. As shown in Figures 6(a) and 6(b), both rGHl and rzGH induced the expression of igfl in the tissue cultures of hepatic caecum and gill in a dose-dependent fashion (compared with control). Moreover, injection of rGHl and rzGH stimulated the expression of igfl in the hepatic caecum (Figure 6(c); compared with control within the same time; the same below), though it had little effect on the expression of igfl in the gill (Figure 6(d)). The reason for this is not clear at present, but one possibility is that rGHl level transported to the gill by circulation might be rather lower because most rGHl had bound to its receptor in the hepatic caecum. Together, these data showed that amphioxus GHl could mediate salinity tolerance via stimulating the expression of igfl.

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Figure 6

Induction of igfl expression by rGHl. (a) Expression of igfl in the cultures of the hepatic caecum in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (b) Expression of igfl in the cultures of the gill in response to rGHl or rzGH (concentrations ranging from 10 ng/ml to 1000 ng/ml). (c) Expression of gh/prllbp in the hepatic caecum of amphioxus injected with saline, rGHl, or rzGH. (d) Expression of igfl in the gill of amphioxus injected with saline, rGHl, or rzGH. Data were from 3 independent experiments and expressed as mean ± SEM. The symbol shows .

3.6. Salinity Increase Induces Expression of ghl, gh/prllbp, and igfl

To test if a vertebrate-like GH-IGF axis is involved in the osmoregulation in amphioxus, we transferred the 25‰ salinity-acclimated animals to seawater with 30‰ salinity and examined the effects of salinity change on the expression of ghl in the Hatschek’s pit and gill as well as gh/prllbp and igfl in the hepatic caecum and gill. No dead animals were observed during the experimental periods. The transfer of 25‰ salinity-acclimated amphioxus to seawater with 30‰ salinity resulted in upregulation of ghl in the Hatschek’s pit (Figure 7(a); compared with control within the same time; the same below) and gill (Figure 7(b)) as well as igfl in the hepatic caecum (Figure 7(e)) and gill (Figure 7(f)). The expression level of gh/prllbp in the hepatic caecum at 48 h after transfer (Figure 7(c)) well matched that of gh expression (Figure 7(a)). However, gh/prllbp expression in the tissue was soon decreased at 72 h after transfer (Figure 7(c)), suggesting that GH/PRLlBP may be also subjected to the downregulation by other factors independent of GHl [35]. Notably, as shown in Figure 7(a), ghl expression was upregulated at 48 h after transfer, but the expression of igfl in the gill at 48 h after transfer was not significantly elevated (Figure 7(f)). These indicated that the hepatic caecum was the primary target tissue of GHl. It should be noticed that even though there was little GHl binding in the gill, nka and nkcc in the gill were still significantly upregulated (Figures 2(c) and 2(d)). These suggested that IGFl, the mediator of GHl secreted by the hepatic caecum, may play a critical role in osmoregulation as IGF-I in fish [20, 21]. Together, all the data suggested that a vertebrate-like GHl/IGF system may be involved in osmoregulation in amphioxus.

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4. Discussion

Functions of GH are diverse, with its growth-promoting and osmoregulatory activities being studied most extensively and intensively [4, 5, 7, 36]. Amphioxus GH-like protein GHl has been shown to have growth-promoting activity. Here, we demonstrate clearly that GHl has the capacity to mediate osmoregulation, as evidenced by the observations that GHl enhances not only survival rate of amphioxus but also muscle moisture under high salinity. In addition, we show that GHl induces upregulation of both the ion transporter NKA and cotransporter NKCC in the gill as well as mediator of GH action IGFl in the hepatic caecum, indicating that GHl apparently fulfills this osmoregulatory activity through the same mechanisms of vertebrate GH. Collectively, these data suggest that osmoregulatory activities of GH already emerged in the basal chordate [37], much earlier than thought before [38].

Teleosts are well adapted for ion exchange using active and passive mechanisms across various surface membranes to keep the osmotic pressure of their body fluids steady when they face relatively hyperosmotic or hypoosmotic environment [39]. Interestingly, Huang [40] has reported that the average osmotic pressure of amphioxus body fluids was about 780 mOsm/L, which was significantly lower than that of ambient seawater, 1200 mOsm/L, suggesting that amphioxus may be able to transport ions across surface membranes to achieve proper osmotic balance and hydration status. However, this demands further study.

The gill, in addition to being a respiratory organ, is the primary site of net sodium and chloride transport in fishes, and the roles of chloride cells in the gill are well accepted as the principal site of ion extrusion in seawater or in a hypertonic environment [18, 41]. The ciliated gill bars of amphioxus are radically different from fish gill structure, and if they function in respiration remains controversial [42–44]. We show that GHl is able to induce the expression of both nka and nkcc as well as gh/prllbp in the gill of amphioxus, suggesting that the gill may also be the main osmoregulatory organ in amphioxus.

GHl has been shown to be the only member of the vertebrate pituitary hormone family in amphioxus, which is capable of promoting growth [26]. Here, we show that GHl is involved in the mediation of osmoregulation. It is apparent that GHl plays a dual role of both growth promotion and osmoregulation. These allow us to propose that the function of the ancestral gene that contributed to the origin of GH/PRL family was to regulate not only somatic growth (i.e., GH-like) but also hydrominal balance (i.e., PRL-like). Thus, the ancestral gene, like amphioxus ghl, might generate two genes by gene duplication early in vertebrate evolution. One of the resulting genes evolved directly into GH gene in modern gnathans, while the other gene evolved into PRL gene, possibly due to adaptation of FW habitats, by genetic innovations and/or mutation after split of agnathans/gnathans (Figure 8). Previously, two models have been suggested to depict the origin of GH/PRL family. The first model was developed on the basis of the examination of vertebrate history and the study of ancient chordates and suggests that the primary function of the ancestral gene that gave rise to the GH/PRL family was GH-like; that is, its original activity was to regulate somatic growth, while PRL activity evolved later, perhaps to allow for the colonization of FW habitats. The opposing view claims that the ancestral gene was involved in osmoregulation, because this one function is common to fish PRL and GH [45]. It is obvious that the two old models become unified in our new model. Of note, only GH but not PRL have been detected in lamprey [46, 47]. Thus, the growth-promoting and osmoregulatory properties of the single hormone remained unchanged in agnathans. Further comparative and functional studies of GH and PRL will shed more light on the divergence and development of these structurally and functionally related hormones and their receptors.

(a)

(b)

Figure 8

A proposed model for the evolution of GH/PRL family. (a) Ancestral GH/GHR system already emerged in the basal chordate, and PRL/PRLR originated with the advent of Gnathostomata. (b) The ancestral gene, like amphioxus GHl gene, generated two genes by gene duplication early in vertebrate evolution. One of the resulting genes evolved directly into GH gene in modern Gnathostomata, while the other gene evolved into PRL gene, possibly due to adaptation of FW habitats, by genetic innovations and/or mutation after split of agnathan/Gnathostomata.

In conclusion, this study highlights amphioxus GHl, in addition to growth-promoting activity, which can mediate osmoregulation through the same mechanisms of vertebrate GH. It also proposes a new model depicting the origin of GH/PRL family in vertebrates.

Conflicts of Interest

The authors declare that there is no interest that could be perceived as prejudicing the impartiality of the research reported.

Acknowledgments

This work was supported by the grants of the Natural Science Foundation of China (31172071) and the China Postdoctoral Science Foundation (2014M561964).

Supplementary Materials

Supplementary Material contains the SDS-PAGE and Western-blotting of rzPRL, sequence information and analysis.

Supplementary Material

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Copyright © 2017 Mengyang Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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