Morphological and molecular evidence for functional organization along the rostrocaudal axis of the adult zebrafish intestine
- Zhengyuan Wang†1, 2, 3,
- Jianguo Du†4, 5,
- Siew Hong Lam2,
- Sinnakarupan Mathavan6,
- Paul Matsudaira1, 2, 3Email author and
- Zhiyuan Gong1, 2Email author
© Wang et al; licensee BioMed Central Ltd. 2010
Received: 8 January 2010
Accepted: 22 June 2010
Published: 22 June 2010
The zebrafish intestine is a simple tapered tube that is folded into three sections. However, whether the intestine is functionally similar along its length remains unknown. Thus, a systematic structural and functional characterization of the zebrafish intestine is desirable for future studies of the digestive tract and the intestinal biology and development.
To characterize the structure and function of the adult zebrafish intestine, we divided the intestine into seven roughly equal-length segments, S1-S7, and systematically examined the morphology of the mucosal lining, histology of the epithelium, and molecular signatures from transcriptome analysis. Prominent morphological features are circumferentially-oriented villar ridges in segments S1-S6 and the absence of crypts. Molecular characterization of the transcriptome from each segment shows that segments S1-S5 are very similar while S6 and S7 unique. Gene ontology analyses reveal that S1-S5 express genes whose functions involve metabolism of carbohydrates, transport of lipids and energy generation, while the last two segments display relatively limited function. Based on comparative Gene Set Enrichment Analysis, the first five segments share strong similarity with human and mouse small intestine while S6 shows similarity with human cecum and rectum, and S7 with human rectum. The intestinal tract does not display the anatomical, morphological, and molecular signatures of a stomach and thus we conclude that this organ is absent from the zebrafish digestive system.
Our genome-wide gene expression data indicate that, despite the lack of crypts, the rostral, mid, and caudal portions of the zebrafish intestine have distinct functions analogous to the mammalian small and large intestine, respectively. Organization of ridge structures represents a unique feature of zebrafish intestine, though they produce similar cross sections to mammalian intestines. Evolutionary lack of stomach, crypts, Paneth cells and submucosal glands has shaped the zebrafish intestine into a simpler but unique organ in vertebrate intestinal biology.
The surface of the intestine epithelium is the site where nutrients are absorbed into the body. This absorption function is aided by expanding the surface area of the gut into villi at the tissue level and microvilli at the cellular level. Consequently, the mouse and human intestine has become a model for studying how this large surface develops during embryogenesis, the role of stem cells in the renewal of the epithelium, and development of colorectal cancer [1–3]. However, these complex problems can be studied in a simpler system, the zebrafish (Danio rerio), which has emerged as an important vertebrate model for study of not only human development but also diseases [4–6].
So far, morphological development of zebrafish intestine has been relatively well characterized in embryos and larvae [7–11], However, the organization and physiology of digestive tract has not been specifically documented for adult zebrafish although several books are available for description of general fish intestine anatomy [12–14]. Zebrafish, like many fish, lacks a morphologically and functionally distinct stomach and does not express genes that encode specific gastric functions [9–12]. Sections of intact zebrafish embryos and juveniles from whole animal serial sections and microCT tomography reveal the digestive tract from pharynx and esophagus to the three sections of the folded intestine and anus [15–17]. Previous studies have described the zebrafish intestine as a tapered tube that begins at the esophageal junction and is folded into three sections, the large diameter rostral intestinal bulb, the mid-intestine, and the small diameter caudal intestine . However, it is not known whether these regions are functionally distinct or whether their functions correspond to the mammalian stomach, small intestine or large intestine. In this study, we characterized the anterior-posterior axis of adult zebrafish intestine at tissue, cellular and molecular levels. By comparing the morphological and molecular characteristics, we identified structurally and functionally distinct areas that correspond to the small intestine and large intestine but not stomach.
Architectural differences along the zebrafish intestinal tract
To characterize intestinal function, we subdivided the intestinal bulb, mid-intestine, and caudal sections into seven segments, S1-S7 (Figure 1B) and examined their architecture under a light microscope. We observe that the zebrafish intestine surface in segments S1-S6 is covered by ridges that are oriented circumferentially across the intestine axis (Figure 1C-1I, as previously reported . The ridges are densely packed and highly branched. In segment S6 the ridges are shorter and broader than the anterior segments. Segment S7 is morphologically distinguished from the other six segments by a smooth surface devoid of any folds or villus-type structures (Figure 1I).
Consistent with our earlier observations of intestinal ridges in segments S1 to S6 and absence of ridges in S7, these ridges in cross-section resemble the spatially separate villi in the mouse or human small intestine (Figure 2). In contrast to the mammalian intestine, crypts are absent from the base of the ridges and specialized crypt cells such as Paneth cells are not observed . The villar ridges are comparable in height from segments S1 to S5 (Figure 2, shorten and broaden in segment S6 (Figure 2F), and absent in segment S7 (Figure 2G). Segments S5-S7 often contain compact excretions that are ensheathed by a mucous layer (stained blue by Alcian Blue in Figure 2G). In addition to the absence of villi, segment S7 is distinguished by its lining of abundant goblet cells that are interspersed by absorptive epithelial cells (Figure 2G). The muscularis externa is apparent, but the mucosa layer, in general, appears very thin compared with other segments of the intestine. Thus, based on histology and architecture, the intestinal lining is divided into three morphologically distinct regions, segments S1-5, S6, and S7.
Distinct molecular signatures along the zebrafish intestinal tract
To understand the significance of the clusters, we then applied a threshold of 2.0 fold against pooled RNA extracted from whole adult zebrafish to the set of 2,558 genes from the ANOVA analysis. This analysis shows the numbers of genes that are abundantly expressed in each individual segment are: 830 (S1), 801 (S2), 820 (S3), 818 (S4), 825 (S5), 950 (S6) and 1023 (S7). To determine the extent to which genes are commonly expressed along the intestinal tract, we determined the overlap in gene sets between pairs of adjacent segments (Figure 3B). Consistent with the clustering results in Figure 3A, significant intersection was found between segments S1-S5 [more than 700 genes (or ≥89.9%) for each overlap, Figure 3B]. However, segments S6 and S7 express quite different sets of genes than the anterior segments. S5 and S6 overlap in 12.3% genes while S6 and S7 share only 45.2% genes in common. Similar results were also observed from analysis of down-regulated genes (Additional file 2).
Molecular features of the small and large intestine-like functions
Having shown the intestine can be subdivided into three regions, S1-S5, S6, and S7, based on similarities in expressed genes, we investigated whether the identity of the genes gives insight into intestine function and thus we selected several intestinal marker genes for more detailed analysis.
The functions of the mouse and human small intestine have been characterized by well known molecular markers including fabp2, vil1l[20–22], apoa1 and apoa4[23–25]. All of these genes were detected in S1-S5 in our microarray analyses by their higher levels of expression compared with total RNAs from whole fish (Figure 4A) and confirmed by real time RT-PCR analyses (Figure 4B-E). Intestinal fabp2 gene encodes a fatty acid binding protein that is specifically involved in the intracellular transport of fatty acids in the small intestine [19, 26, 27]. This gene is highly conserved in teleosts, amphibians, avians and mammals . Previously, an RFP transgenic zebrafish line under the intestinal fabp2 promoter, Tg(fabp2:RFP), has been generated and RFP reporter gene is specifically expressed in the intestine . To further verify the expression of intestinal fabp2, we isolated an intestine from a 3-month-old Tg(fabp2:RFP) transgenic zebrafish and found that RFP fluorescence was high in segments S1-S4, but quickly diminished around the second turn of the intestine (Additional file 3, Panel B). This expression pattern was also confirmed by direct detection of endogenous fabp2 mRNA expression by in situ hybridization (Additional file 3, Panel C). Closely resembling the pattern of fabp2 expression, villin expression is also restricted to the mammalian gastrointestinal tracts where it is highly expressed in the small intestine . Our microarray data show that zebrafish villin gene (vil1l) is highly expressed in segments S1-S5 and its expression is reduced in segments S6 and S7. This finding is further validated by real time RT-PCR (Figure 4C), where the expression of vil1l decreases in segment S5 and to a negligible level in segments S6 and S7. In further support that segments S1-S4 possess features of a small intestine, another two conserved markers, apoa1 and apoa4, also showed similar expression pattern to fabp2 and vil1l genes along the anterior-posterior axis of zebrafish intestine. These two genes can also be considered to be reliable molecular markers for small intestine because in 36 human tissues and 45 mouse tissues examined, expression of mammalian Apoa1 and Apoa4 are highly restricted to the digestive organs including small intestine and liver (GSE2361 and GDS182, GEO database, NCBI). These patterns of small intestine markers together with the transcriptome data suggest that the small intestine comprises segments S1-S4 and transition into a different function occurs in segment S5.
If segments S1-S4 are small intestine-like, then we investigated whether S5-S7 expresses gene markers for the large intestine. Two genes, cfl1 (cofilin1) and aqp3 (aquaporin 3), distinguish segments S5-S7 from S1-S4. Cfl1 belongs to a family of actin-binding proteins and mediates dynamic stabilization of actin filaments . Our microarray and real time RT-PCR data (Figure 4A, F) indicate that cfl1 is primarily expressed in segments S5-S7, but down-regulated in the first four segments. Analysis of rat EST database suggests that cfl1 is expressed in the large intestine but not in the small intestine (Unigene's EST profile viewer, Unigene Rn.11675, NCBI). Similarly, our microarray data indicated increased expression of Aqp3, an osomoregulatory channel protein on membrane of epithelial cells , particularly in the large intestine of mammals  and mucus cells of the posterior intestine of teleost eel , in segments S6 and S7 (Figure 4A, Dr.76207). Aquaporins are water channel proteins that facilitate water movement, hence increase water permeability, across cell membrane and the increase expression of Aqp3 is therefore important for absorption of water in the intestine, in particular, for the faecal dehydration in the large intestine. In line with this, the mammalian aquaporin 3 is expressed along the gastrointestinal tract, with its highest expression in the colon [31, 32]. Thus, while segments S1-S5 possess molecular features of small intestine, segments S6 and S7 have molecular features of large intestine with segment S5 as a transitional region).
Analysis of gene ontology (GO) along the anterior-posterior axis
To infer the functions of the intestinal segments, 2-fold up-regulated genes against the whole fish reference RNA were extracted for the three groups, S1-S5 (891 genes), S6 (1147 genes), and S7 (1107 genes). We envision that these significantly up-regulated genes should better represent specific functions of different intestinal segments and thus gene ontology analyses were carried out for these genes using GOTree Machine . Significantly enriched (p-value < 0.01) categories in each region are shown in Additional file 4.
As expected from a major metabolic organ, the intestine of zebrafish harbours a rich collection of genes involved in metabolism, molecular transport and localization, catalytic activities among others. However, major differences were found between the three groups of S1-S5, S6 and S7. There are 56 categories that were statistically enriched in S1-S5, but only 6 categories in S6 and 8 categories in S7. Among these enriched categories, up-regulated genes in S1-S5 are involved in a wide range of metabolic processes, including metabolism of fatty acid, organic acid, lipid, vitamin, heme, alcohol, glucose, hexose, monosacchride, carbohydrate, etc. (Additional file 4). They also play important roles in energy generation and homeostasis of ion, iron and cations. Notably, a group of genes are associated with catalytic activities such as hydrolase activity and transferase activity, which are important for the absorptive function of the small intestine. The variety of GO categories in the S1-S5 group supports the multiple functions of this part of zebrafish intestine with features of the small intestine (to be discussed below).
The S6 and S7 groups, on the other hand, only show a few statistically enriched categories. For example, genes from S6 are involved in oxidoreductase activities while genes from S7 are enriched in biosynthesis of vitamin and pyridine nucleotide (Additional file 4). They are also involved in intracellular signaling and pentosyl/phosphoribosyl transferase activity. It seems that segments S6 and S7 represent two regions of zebrafish intestine that perform tasks apparently different from those of S1-S5.
Cross-species Gene Set Enrichment Analysis (GSEA) indicates the segments S1-S5 to be multi-functional
Comparison of transcriptome similarity of zebrafish intestinal segments and human/mouse intestines by GSEA analyses
Zebrafish intestinal segments#
Mouse small int.
Human small int.
Human sigmoid colon
In contrast to segments S1-S5, segment S6 closely resembles the cecum and rectum of the human large intestine (FDR < 0.001), while segment S7 resembles human rectum only (FDR = 0.003). Gene ontology analysis shows that S6 resembles human cecum in glycolysis, oxidoreductase activity, metabolism of amino acid, amine derivative, organic acid, carboxylic acid and alcohol. While in S7, metabolism of membrane lipid was found to be enriched. Water retention is a common function in mammalian large intestine. Consistent with this, several aquaporin genes, including aquaporins 1, 3 and 10 are highly expressed in S6/S7. In particular, Aquaporin 3 is well known a key component of faecal dehydration in mammalian colon [31, 32]. Interestingly, although S1-S5 most closely resembles the small intestine, we detected some significant similarity with functions found in the human colon and rectum (Table 1), suggesting that the zebrafish segments S1-S5 may have broader functions. This phenomena may reflect the less specialized and differentiated features of fish intestine as a primitive species of vertebrates. This is particularly true for fish "small intestine" (S1-S5) as it constitutes more than two thirds of the length of the intestine.
In summary, GSEA analysis supports that segments S1-S5 of zebrafish intestine possess features of a mammalian small intestine, while segments S6 and S7 possess features of a mammalian large intestine (with S7 resembling rectum in particular).
Stomach-like functions of the intestine
Whereas pepsinogen is not encoded in the zebrafish genome, other stomach markers may be expressed by the intestine. For example, lipf is a gastric lipase gene encoding an acidophilic lipase known to be secreted by mammalian gastric chief cells [41, 42]. Its expression in human is restricted to esophagus, stomach and several other tissues, but not in the intestine (Unigene's EST profile viewer, UniGene Hs.523130, NCBI database). In contrast, lipf is expressed in all seven segments of the zebrafish intestine and not restricted to any particular segment (Figure 4A).
For comparison of similarity between zebrafish fragments, we used differentially expressed genes generated by ANOVA (Figure 2 and Additional file 2). For GO (Additional file 4) and GSEA (Table 1) analyses, we selected 2-fold up-regulated genes against the reference RNA (total whole adult fish RNA) and this selection was independent of the initial set of differentially expressed genes selected by ANOVA for similarity analyses. Our approach would filter out ubiquitously expressed housekeeping genes. Abundantly expressed intestine-specific or enriched transcripts will be retained by the 2-fold selection as their concentrations in the total fish RNA pool would be diluted much more than 2 fold. We have also tried 1.5-fold selection, basically the same GSEA results were obtained (data not shown).
The results in this study document that the zebrafish intestine is regionally segmented into a small intestine and large intestine. This conclusion is supported by morphology and three lines of independent analysis of gene expression profiles from seven segments of the intestine. Clustering analysis reveals a general similarity between S1-S5 and differences between S6 and S7 and the degree of similarity is measured by the degree of overlap in gene sets expressed in neighboring segments. Second, we showed that well-known markers of the mammalian small and large intestine such as villin, fabp2, and cof1 are differentially expressed along the anterior-posterior axis. Finally by ontologies of genes expressed in the segments are consistent with small and large intestine function and confirmed by whole transcriptome comparisons with human and mouse small and large intestine gene sets. Based on these findings, we suggest that the intestinal bulb, mid-intestine, and the anterior third of the caudal intestine corresponds to the small intestine of the mammalian gut while the remaining posterior portion of the caudal intestine corresponds to the large intestine terminating with the rectum.
In comparison with the mammalian intestine, the zebrafish intestine has a simple architecture with the intestinal lining folded into villar ridges rather than distinct finger-shaped villi of the mammalian small intestine. In cross section, a ridge appears identical to a villus and thus may be an evolutionary precursor to discrete villi. In support of this idea, an intermediate stage (from D8-D8.5) in the morphogenesis of the chick intestine includes the initial formation of longitudinally oriented previllous ridges that buckle into a zig-zag pattern and eventually form villi in adult intestine. Thus, in birds, ridges are embryological precursors to villi .
In addition to the lack of well-defined villi, the zebrafish intestine lacks well-defined crypts, infoldings of the intestinal surface where stem cells and proliferating cells are located [8, 9]. Intestinal crypts are normally found at the base of the villus or lining the colon of the large intestine. In the zebrafish intestine, mitosis is restricted to the base of the villar ridges ([9, 10] and our unpublished data), suggesting that the Crypts of Lieberkuhn are specializations of the mammalian intestine. This arrangement also raises questions about the dynamics of epithelial renewal because cell proliferation in the intestine is balanced by apoptosis at the villus tips. Location of apoptosis in the adult zebrafish intestine is rarely reported but we find most cell death occurs in the distal portion of the villar ridges and apoptosis is much more active when compared with mammalian intestines (our unpublished data). In contrast, apoptosis in the embryonic and larval zebrafish intestine goes undetectable until morphogenesis has completed [8, 9], while apoptosis occurs throughout the development of the mouse duodenum  but is reduced to a few cells per villus during adulthood .
Like many other fish including cyprinids and others , the zebrafish has evolved into a stomachless fish . The absence of a functional pepsinogen gene from the digestive tract is not unique to zebrafish but also occurrs in medaka fish (Oryzias latipes) and other stomach-less fishes. Interestingly, the expression of pepsinogen gene in another stomchless fish, the puffer fish (Takifugu rubipes), is restricted to its skin tissue, adopting different functions . Without a stomach, digestion and absorption must begin as early as possible in the limited length of the zebrafish digestive tract. Ingested food is temporarily stored in the rostral intestinal bulb that bulges like an elastic sac, where food starts to be broken down in the absence of a stomach  and the entire length of the intestine may serve to degrade food.
Based on analysis in larval zebrafish and other cyprinids, previous reports raised that the posterior zebrafish intestine may be analogous to the mammalian colon [48, 49]. This has also been proposed in a recent study based on histological data and molecular markers . Here our transcriptome data provide more solid evidence that this part of intestine in adult zebrafish resembles mammalian colon and rectum and moreover, segments S6 and S7 distinguish themselves from each other.
In the present study, the entire intestine of adult zebrafish was systematically examined at the levels of anatomy, histology and transcriptome. Despite the lack of crypts and evident structural distinction throughout most of the length of intestine, our genome-wide gene expression data have shown that the rostral, mid, and caudal portions of the zebrafish intestine have distinct functions analogous to the mammalian small and large intestine, respectively. Organization of ridge structures represents a unique feature of zebrafish intestine, though they produce similar cross sections to mammalian intestines. Evolutionary lack of stomach, crypts, Paneth cells and submucosal glands has shaped the zebrafish intestine into a simpler but unique organ in vertebrate intestinal biology. This scenario may represent an evolutionary primitive feature of the digestive tract, where functional regionalization precedes morphological regionalization in a low vertebrate.
Maintenance of zebrafish and dissection of zebrafish intestine
Danio rerio of about one year old were maintained following established protocols  and in compliance with Institutional Animal Care and Use Committee (IACUC) guidelines. Zebrafish were euthanized by 0.1% 2-phnoxyethanol and their intestines were isolated and cut into seven segments along the anterior and posterior axis, as shown in Figure 1B. The seven segments were labeled S1, S2, S3, S4, S5, S6 and S7, respectively.
Paraffin sectioning of zebrafish intestine
Intestinal segments were fixed in 4% paraformaldehyde in phosphate buffered saline at room temperature overnight. Then the intestine samples were dehydrated in 70% ethanol overnight and further dehydrated in ethanol with increasing gradients (75%, 90%, 95% and 100%). The samples were cleared in 100% Histoclear II (National Diagnostics, US) for 30 min twice, embedded in liquid paraffin at 58°C for 30 min, then changed into fresh paraffin for final embedding at 58°C overnight. Finally, the samples were sectioned at 7 μ m on a Reichert-Jung 2030 microtome (Leica, Germany) and collected onto Fisher SuperFrost slides. The slides were left on a heating block at 42°C overnight before further assays were conducted.
Hematoxylin & Eosin & Alcian blue staining
Tissue sections were stained by Meyer's hematoxylin for 10 min, rinsed in tap water, stained by eosin for 1 min, followed by dips in acidic ethanol and rinse in tap water. They were stained by alcian blue (Biogenex, US) for 10 min and rinsed in tap water. Finally, the slides were dehydrated in ethanol of increasing gradients (75%, 90%, 95% and 100%), cleared by HistoClear II (National Diagnostics, US), mounted with DePeX (EMS, US) mounting medium and covered by coverslips. Images were taken using a Zeiss Axiovert imaging system.
Quantitative real-time PCR
Quantitative real-time PCR was carried out in 96-well plates on a LightCycler 480 system (Roche, Swiss). The PCR reaction was set up according to the manufacturer's protocol with optimization of primer-specific annealing temperature and extension time. PCR products were labeled by SYBR Green dye. All gene expression levels were measured and normalized against the level of house-keeping gene bactin1 expression.
Intestines were isolated from male adult zebrafish, quickly rinsed in 1× phosphate buffered saline/diethylpyrocarbonate, and cut into seven segments according to Figure 1B. To maintain a more homogenous molecular background, only male fish were used for microarray analyses. The same segments from every 10 fish were pooled as one biological replicate and they were kept in liquid nitrogen till extraction of RNA. RNA was double-extracted using Trizol (Invitrogen, USA). A total of five replicates were prepared for each segment. For each replicate, 10 μ g RNA was reverse-transcribed into cDNA with incorporation of aminoallyl-dUTPs. Later the samples were hybridized onto in-house spotted microarray chips with labeling by Cy5 as described previously . RNAs from whole fish were used as reference for all experiments and labelled by Cy3. The arrays contained 22 K oligonucleotide probes where 16.4 K probes were designed by Compugen (USA)  and the remaining probes were in-house designed by the bioinformatics group in Genome Institute of Singapore (GIS). The complete list of gene probes has been submitted to GEO database with the access number GSE20884. For each gene probe, one 65-mer oligonucleotide probe was designed from the 3' untranslated region for maximizing gene specificity. 172 copies of the beta-actin gene probe were included in each array as calibration spots. All of the oligonucleotide probes were synthesized from Sigma and spotted on glass slides using the Genemachine robotic spotter/arrayer (Genomic Solutions, Ann Arbor, MI, USA) housed at GIS . After hybridization, the microarray chips were scanned and graded, and raw data went through two rounds of normalization: They were first normalized within each single array and second normalized across the whole collection of arrays, using LOWESS method implemented in Gene Cluster 3.0 during the pre-processing stage.
Identification of differentially expressed genes from the microarray data
Pre-processed microarray data were visualized and subjected to one-way ANOVA test using MeV MultiExperiment Viewer software . One-way ANOVA test was performed using a critical p-value of 0.1 with standard Bonferroni correction for all seven intestinal segments. The selected genes were used for clustering and expression pattern analysis to compare the similarity and differences in the seven segments.
Gene ontology (GO) analysis by GO Tree Machine
Up-regulated genes were selected for each individual segment based on the fold changes of their expression levels (at least two told up against the RNA of pooled adult zebrafish and FDR adjusted p-value < 0.05). Gene ontology was carried out using GOTree Machine, which is a web-based tool developed by the Vanderbilt University to analyze gene ontology for a given set of genes . It compares the distribution of genes in the gene set of interest in each GO category to those in the reference gene set, i.e. the transcriptome of zebrafish in our case. Gene information was retrieved from GeneKeyDB, a database that integrates gene information from Ensembl, Swiss-Prot, HomoloGene, Unigene, Gene Ontology Consortium and Affymetrix etc. Statistical tests were used for the assessment of enrichment of each gene category.
Gene Set Enrichment Analysis (GSEA)
GSEA is a computational method that determines whether a priori defined set of genes shows statistically significant, concordant differences between two biological samples; it calculates an enrichment score using a running-sum statistic through a ranked list of gene expression data set . In this work, the software GSEA2.0 developed by the Broad Institute  was used. The statistical significance of the enrichment score was estimated by using an empirical phenotype-based permutation test procedure. A false discovery rate was provided by introducing adjustment of multiple hypothesis testing.
The authors would like to thank Singapore-MIT Alliance, BioMedical Research Council (BMRC) of Singapore and National University of Singapore for support of this work. ZW is supported by a SMA scholarship and JD by a Visiting Scholarship from P.R. China. The authors also wish to thank Ms Mya Myintzu Hlaing for assistance in microarray processing and Dr Ung Choong Yong for pre-processing of the microarray data. The microarray data reported in this paper have been submitted to GEO database with the access number GSE20884.
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