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Originally published as JHC exPRESS on November 26, 2007.
doi:10.1369/jhc.7A7310.2007
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Journal of Histochemistry and Cytochemistry
Volume 56 (3): 275-283, 2008
Copyright ©The Histochemical Society, Inc.

Immunohistochemical Localization of Collagen Type XI {alpha}1 and {alpha}2 Chains in Human Colon Tissue

Kara B. Bowen, Aaron P. Reimers, Sarah Luman, Joseph D. Kronz, William E. Fyffe and Julia Thom Oxford

Department of Biology, Northwest Nazarene University, Nampa, Idaho (KBB,APR,SL,WEF); Department of Pathology, Mercy Medical Center, Nampa, Idaho (JDK); and Department of Biology, Biomolecular Research Center, Boise State University, Boise, Idaho (JTO)

Correspondence to: Julia Thom Oxford, Department of Biology, Biomolecular Research Center, Boise State University, 1910 University Drive, Boise, ID 83725. E-mail: joxford{at}boisestate.edu


   Summary
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 Summary
Introduction
 Materials and Methods
 Results
 Discussion
 Literature Cited
 
In previous studies, collagen XI mRNA has been detected in colon cancer, but its location in human colon tissue has not been determined. The heterotrimeric collagen XI consists of three {alpha} chains. While it is known that collagen XI plays a regulatory role in collagen fibril formation, its function in the colon is unknown. The characterization of normal human colon tissue will allow a better understanding of the variance of collagen XI in abnormal tissues. Grossly normal and malignant human colon tissue was obtained from pathology archives. Immunohistochemical staining with a 58K Golgi marker and {alpha}1(XI) and {alpha}2(XI) antisera was used to specifically locate their presence in normal colon tissue. A comparative bright field microscopic analysis showed the presence of collagen XI in human colon. The juxtanuclear, dot-like collagen XI staining in the Golgi apparatus of goblet cells in normal tissue paralleled the staining of the 58K Golgi marker. Ultra light microscopy verified these results. Staining was also confirmed in malignant colon tissue. This study is the first to show that collagen XI is present in the Golgi apparatus of normal human colon goblet cells and localizes collagen XI in both normal and malignant tissue. Although the function of collagen XI in the colon is unknown, our immunohistochemical characterization provides the foundation for future immunohistopathology studies of the colon. (J Histochem Cytochem 56:275–283, 2008)

Key Words: collagen type XI • colon • immunohistochemistry • Golgi apparatus • 58K Golgi marker


   Introduction
Top
 Summary
 Introduction
Materials and Methods
 Results
 Discussion
 Literature Cited
 
COLLAGEN XI is best characterized in its molecular assemblies with structural collagens type II and IX to form fibrils in cartilage (Miller and Gay 1987Go; Mendler et al. 1989Go). Proper formation of collagen fibrils is reliant on collagen XI's regulatory function (Li et al. 1995Go; Wu and Eyre 1995Go). Collagen XI, a heterotrimeric molecule, consists of {alpha}1, {alpha}2, and {alpha}3 collagen chains. The {alpha}1(XI) and {alpha}2(XI) chains are distinct gene products, whereas {alpha}3(XI) is a hyperglycosylated form of the {alpha}1 chain of collagen II (Burgeson and Hollister 1979Go; Morris and Bächinger 1987Go). Initially synthesized as a procollagen, collagen XI's amino and carboxyl termini are subsequently proteolytically removed (Sussman et al. 1984Go; Thom and Morris 1991Go). Both {alpha}1(XI) and {alpha}2(XI) have an amino terminal domain (NTD) that can be further subdivided into the amino-propeptide (Npp) and the variable region (Vr). The {alpha}1(XI) Vr exists as a set of potentially eight different splice forms that arise by alternative splicing of mRNA between exons 6a, 6b, 7, and 8, encoding the corresponding protein regions p6a (V1a), p6b (V1b), p7 (C2), and p8 (V2) (Figure 1 ) (Oxford et al. 1995Go; Zhidkova et al. 1995Go).


Figure 1
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  		Figure 1

Schematic diagram of collagen ({alpha}1)XI amino terminal domain. Approximate locations of target sequences are indicated for each of the antisera used for this study. The V1a region is recognized by antiserum 5551, the V1b region is recognized by antisera 1702 and 6834, the C2 region is recognized by antiserum 8691, and the V2 region is recognized by antiserum 1703.

 
Accessing the major triple helix of collagen XI is not possible without disrupting the fibrils, but the NTD is exposed on the fibril surface. The NTD remains on the surface for an extended period of time after biosynthesis (Thom and Morris 1991Go; Keene et al. 1995Go). Preliminary data have indicated that the proteolytic removal rate of the {alpha}1(XI) Npp is dictated by the splice forms present in the Vr (Medeck et al. 2003Go). This function requires the Vr to be on the fibril surface (Gregory et al. 2000Go). The fibril surface location of the NTD facilitates immunohistochemical localization.

The presence of collagen XI has been studied in both cartilaginous and non-cartilaginous tissue, such as human chondrocytes (Burgeson and Hollister 1979Go; Swoboda et al. 1989Go; Lui et al. 1995Go), skeletal muscle (Lui et al. 1995Go), placenta (Bernard et al. 1988Go; Yoshioka and Ramirez 1990Go; Oxford et al. 1995Go), lung (Lui et al. 1995Go; Chong et al. 2006Go), and brain (Lui et al. 1995Go), and collagen XI mRNA has been shown to be upregulated in colorectal cancer (Fischer et al. 2001aGo,bGo). Fischer et al. (2001a)Go concluded through northern blotting and RT-PCR that collagen ({alpha}1)XI was not present in the adult human colon, and Sandberg et al. (1993)Go concluded through Southern blotting that {alpha}2(XI) is not present in the fetal colon. Although both of these support the hypothesis that collagen XI is not produced in the colon, it is possible that collagen XI was either below the limit of detection by the experimental technique or is posttranslationally relocated within the cells of the colon. Detailed structural localization of the components of the collagen ({alpha}1)XI Vr in normal and malignant colon tissue using immunohistochemical staining has not been published to date. To evaluate the upregulation of collagen XI observed in cases of colorectal cancer, it is advantageous to document the presence in both normal and malignant tissue.


   Materials and Methods
Top
 Summary
 Introduction
 Materials and Methods
Results
 Discussion
 Literature Cited
 
Antisera
Using specific {alpha}1(XI) chain antisera allowed a circumspect observation of collagen XI presence. Antibodies were raised against a 20-aa synthetic peptide designed from the amino portion of V1b (exon p6b), a 20-aa synthetic peptide from the carboxyl portion of V1b (exon p6b), and a 39-aa synthetic peptide from V1a (exon p6a) of the collagen {alpha}1(XI) chain as described previously (Oxford et al. 1994Go; Keene et al. 1995Go, Davies et al. 1998Go). All antisera were initially characterized by ELISA to verify that the antibodies recognized the target peptides and to determine titer, that they did not recognize similar but unrelated peptides, and that they had the capacity to recognize the target protein by immunoblot and immunofluorescence against tissues and cells from several species including human, bovine, horse, chicken, mouse, and rat. Other antibodies raised against the 14-aa bovine sequence of the collagen {alpha}2(XI) chain (Oxford et al. 2004Go), a 29-aa synthetic peptide from C2 (exon p7) (Oxford et al. 1994Go; Morris et al. 2000Go), and a 20-aa human synthetic peptide from the carboxyl portion of V2 (exon p8) (Davies et al. 1998Go) were characterized by ELISA, immunoblot, and immunofluorescence staining on cells and tissue sections previously as indicated above. A 58K Golgi protein monoclonal antibody, formiminotransferase cyclodeaminase, (6284; Abcam, Cambridge, MA), was used for a side-by-side comparison with the collagen XI antibodies.

The percent of sequence identity of peptide antigen and human target was determined using BLAST 2 sequences (http://www.ncbi.nlm.nih.gov/blast/bl2seq/wblast2.cgi), where the known sequence of each antigen was compared with the human collagen XI {alpha}1 or {alpha}2 chains. In addition, each antigen sequence was used (http://www.ncbi.nlm.nih.gov/BLAST) to identify any proteins that could potentially introduce artifactual staining results.

Colon Tissue
Grossly normal and malignant human colon tissue, removed of identity in accordance with institutional review board guidelines, was obtained from pathology archives (Mercy Medical Center; Nampa, ID). Tissue was fixed with formalin containing zinc, paraffinized, cut to 1 µm thickness, and heat fixed onto glass slides, as previously described (Fyffe et al. 1999Go).

Immunohistochemical Staining
The colon tissue slides were deparaffinized through incubation in a VWR incubator (model 1320; Sheldon Manufacturing, Cornelius, OR) for 25 min at 65C. Deparaffinization and rehydration was carried out through sequential washes in xylene (twice at 5 min), absolute ethanol (twice at 3 min), 95% ethanol (twice at 3 min), and distilled water for 5 min. For the remainder of the procedure, the tissues were maintained in a humidified chamber and not allowed to dry out. A Pap Pen (DakoCytomation; Dako North America, Carpinteria, CA) was used to ensure that the solution remained on the slide.

Hyaluronidase (H3506; Sigma-Aldrich Corporation, St. Louis, MO) was diluted to 0.01 mg/ml with Tris-buffered saline (TBS), pH 7.5 (0.2 M Tris, 0.17 M NaCl); 200 µl was placed on each slide to incubate in a Slide Moat (Boekel Scientific; Feasterville, PA) at 25C for 45 min. Subsequent 25C incubations also used this slide moat. Slides were rinsed with TBS and distilled water and subsequently placed into 95–99C target retrieval solution, pH 7.5, (DakoCytomation; Dako North America) for 40 min. The slides were allowed to cool in the target retrieval solution for 20 min and were rinsed with fresh Wash Buffer, a TBS saline solution containing 0.05% Tween 20 (DakoCytomation; Dako North America). To quench endogenous peroxidases, the slides were incubated with 200 µl Dual Endogenous Enzyme Block for Autostainer (DakoCytomation; Dako North America) for 25 min at 25C, rinsed with fresh Wash Buffer, and submerged in Wash Buffer three to five times.

Each primary antibody was diluted with antibody diluent (DakoCytomation; Dako North America) to a dilution optimized by serial dilutions (1:300 for carboxyl V2; 1:400 for V1a and C2; 1:450 for amino and carboxyl V1b, and {alpha}2). The tissue was incubated in 200 µl primary antibody for 1 hr at 25C and rinsed as was done subsequent to enzyme block incubation. A positive control of placental tissue (Bernard et al. 1988Go; Yoshioka and Ramirez 1990Go) and a negative control of only secondary antibody coincided with this process. EnVision+ Dual Link System Peroxidase (DakoCytomation; Dako North America), an anti-rabbit and anti-mouse secondary antibody, was applied, 200 µl/slide, and incubated at 25C for 30 min. The slides were rinsed with Wash Buffer. Liquid DAB+ Substrate Chromagen System for Autostainer (DakoCytomation; Dako North America) was added, 200 µl/slide, to each slide. After a 20-min incubation at 25C, the slides were rinsed with distilled water. Each slide was placed in hematoxylin (Hematoxylin 7211; Richard-Allan Scientific, Kalamazoo, MI) for 2 min, rinsed thoroughly with distilled water, and placed in distilled water for 5 min.

The tissue was dehydrated through graded ethanol-concentration steps and xylene. Glass coverslips were glued (Pro-Texx Mounting Medium; Baxter Diagnostics, Deerfield, IL) over tissue to enhance preservation of the tissue. Ultra light microscopy was carried out using a Leica DM500 microscope (Leica Microsystems; Bannockburn, IL) with a 1.6-cm resolving lens, x10 optical, x1.25 magnifier, and a x100 (numerical aperture, 1.46) objective. This allows for x2000 magnification.


   Results
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 Summary
 Introduction
 Materials and Methods
 Results
Discussion
 Literature Cited
 
Characterization of {alpha}1(XI) and {alpha}2(XI) Antisera
The antibody specificity has been previously established (Keene et al. 1995Go; Oxford et al. 1995Go; Davies et al. 1998Go). BLAST results indicated that peptide antigen sequences were highly conserved between rat and human and between bovine and human for the sequences of interest (Figure 2 ).


Figure 2
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  		Figure 2

Comparison of collagen XI antigen sequences to humans. Vertical lines indicate identical residues. Dots represent dissimilarities in sequences, although aa have similar properties. Spaces in sequence denote gaps introduced for alignment of the sequence. Dashes in conserved sequence indicate nonconserved residues. The published consensus sequence between bovine, human, mouse, chicken, and rat, when available, is presented below each sequence (Medeck et al. 2003Go). Fraction and percent identity included missing aa as a deviation.

 
Each antigen sequence was compared with the human genome through BLAST searches to find any proteins that have similarities to collagen XI. Mitogen-activated protein kinase (MAPK) (accession number BAD92330) has a similar sequence to the p6a antigen (EYDYEY). Titin (accession number Q8WZ42), a muscular fiber protein, has multiple short sequences in common with the antigen to the carboxyl end of p8 (GPGVP). Mib (accession number BAF03565), a newly discovered brain membrane protein, also has a similar sequence to p8 (GPGVPA). The potential targets identified by BLAST searches are less likely targets than the intended collagen {alpha}1(XI) targets of the polyclonal antisera used in this study.

Collagen XI Staining in the Golgi Apparatus of Colonic Crypts
Presence of the collagen XI {alpha}1 and {alpha}2 in normal and malignant colon tissue was visualized using antibodies against the {alpha}1(XI) splice forms and the {alpha}2(XI) {alpha} chain (Figures 3 and 4) . From the staining and analysis, it was evident that there was specific staining present in normal colon tissue. Each of the collagen XI antibodies yielded intense juxtanuclear, dot-like staining within the colonic crypts epithelial cells, accompanied by diffuse, light cytoplasmic staining and a lack of stromal staining (Figure 3). Furthermore, malignant colon tissue showed the presence of {alpha}1(XI) splice forms and the {alpha}2(XI) {alpha} chain, although appearing more cytoplasmic in comparison to the juxtanuclear, dot-like staining seen in normal tissue. Malignant colon tissue and placental tissue served as positive controls for staining of each antibody. The negative control using antiserum-diluent in place of the primary antibody did not stain (Figure 3H).


Figure 3
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  		Figure 3

Collagen ({alpha}1)XI colonic staining. Novel antibodies, raised against each splice form of the variable region of collagen ({alpha}1)XI, were used to locate specific collagen markers in normal colon tissue. Human malignant colon tissue is shown for comparison (F). A low-magnification image is included to allow evaluation of potential staining of lymphatic and blood vessels and stromal cells (E). Each antibody displays juxtanuclear dot-like staining within goblet cells of the colonic crypt. (A,E) V1a (5551). (B,F) Amino portion of V1b (1702), normal and malignant, respectively. (C) V2 (1703). (D) C2 (8691). (G) Placenta positive control (1703). (H) Negative control (no 1° antibody). Bar = 25 µm.

 

Figure 4
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  		Figure 4

Comparison of {alpha}l(XI) and {alpha}2(XI) to the 58K Golgi marker. Bright field microscopy images show the presence of collagen XI in the Golgi apparatus of human colon tissue. Human colon cancer tissue is shown for comparison (E,F). Note the intense, juxtanuclear dot-like staining in both {alpha}l(XI) and {alpha}2(XI) seen in the Golgi apparatus region of the goblet cells of normal colon tissue, as seen for the 58K Golgi marker. (A,E) Carboxyl V1b (6834), normal and malignant tissue, respectively. (B,F) {alpha}2(XI), normal and malignant tissue, respectively. (C) 58K Golgi marker. (D) Negative control (with no 1° antibody). Bar = 25 µm.

 
Juxtanuclear staining in normal colon tissue was located in the same subcellular area as the Golgi apparatus of colonic epithelial cells as confirmed by the 58K Golgi marker (Figure 4). A staining comparison of each collagen XI antibody and the 58K Golgi marker at high magnification reiterated Golgi apparatus staining (Figure 5 ).


Figure 5
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  		Figure 5

Focal examination of a normal colonic crypt. (A) High magnification of a typical goblet cell of the colon stained with 58K Golgi marker. The oval identifies one goblet cell. Note the polar configuration of organelles with the nucleus (N) in the basal region, the juxtanuclear Golgi apparati (G), and the secretory granules (Sg) that accumulate in the apical portion of the cell. (B) Typical colonic crypt stained with collagen XI V1a antibody (5551). (C) Zoom of circled region from B. (D) The same colonic crypt as shown in B in a consecutive slice of tissue stained with 58K Golgi marker. (E) Zoom of circled region in D. A comparative analysis of these photos verifies the colocalization of the Golgi marker and our collagen XI antisera. Bar = 25 µm.

 

   Discussion
Top
 Summary
 Introduction
 Materials and Methods
 Results
 Discussion
Literature Cited
 
Collagen XI is a minor but essential constituent of collagen fibrils because of its well-characterized role in the regulation of fibril diameter (Morris and Bächinger 1987Go; Mendler et al. 1989Go). Its function is less well understood in non-cartilaginous tissues. The NTD of the {alpha}1(XI) chain remains attached to the rest of the molecule for a longer period of time after synthesis than the other amino propeptides of fibrillar collagens and has been localized to the surface of thin collagen fibrils (Keene et al. 1995Go). Because the NTD of collagen XI is exposed at the surface of collagen fibrils, antisera against various sequences within the NTD of {alpha}1(XI) and {alpha}2(XI) were used. Although best characterized for its role in cartilage, the presence of collagen type XI within colon tissue may be relevant in the onset of inflammatory bowel disease, including ulcerative colitis and Crohn's disease, and may in part explain the link between intestinal and extraintestinal manifestations common in articular joints and the eyes. Collagen XI may be considered a candidate for an autoantigen or the target of an aberrant self-recognition that contributes to an exaggerated inflammatory response by the adaptive immune system. Additionally, changes in collagen XI expression as a function of colon cancer progression may provide the opportunity for development of new diagnostic reagents.

In this study, immunostaining has been shown by bright field microscopy in normal and malignant colon tissue using collagen XI polyclonal antibodies against the splice forms of {alpha}1(XI) and the {alpha}2(XI) {alpha} chain. In normal colon tissue, juxtanuclear, dot-like staining has revealed collagen XI localized to the Golgi apparatus. A review of the literature indicated that this is the first confirmation of collagen XI staining in normal colon tissue. A Golgi marker, raised against a resident enzyme (58K, formiminotransferase cyclodeaminase), confirmed the location of Golgi apparatus in goblet cells, which mirrored the collagen XI staining locale. Ultra light microscopy also explicated the Golgi apparatus staining.

In comparing normal and malignant colon tissue staining with collagen XI antisera, there was an apparent decrease of Golgi staining and an increase of cytoplasmic staining in cancerous tissue compared with normal colon tissue. Further studies will investigate the statistical significance of these apparent differences in localization and intensity of collagen XI staining in normal and malignant tissue. It is possible that a dysregulation of protein localization within cells may accompany tumor progression and result in the changes observed.

Potential artifacts caused by cross-reactivity of the antisera were studied; however, no likely alternative targets for the antisera used in this study were identified. Titin, a cytoskeletal protein, has not been found in the colon or the Golgi and is therefore an unlikely candidate for cross-reactivity with the antibody to the carboxyl end of V2. Mib, a novel cerebral membrane protein, first found in senile plaques, was discovered by Satoh et al. (2006)Go and was shown to be present in colon among other tissues. Through colocalization with markers for endoplasmic reticulum (ER), ER–Golgi intermediate compartment, and cis-Golgi, it was determined that Mib is present in the ER and intermediate compartments but does not enter into the Golgi. Although this protein is present in the colon, because this protein does not reside in the Golgi, it is improbable that it cross-reacts with the collagen XI antibody to carboxyl V2. MAPK is a ubiquitous protein that activates processes through phosphorylation in response to a variety of cellular stimuli. BLAST search indicated a slight potential for cross-reactivity with MAPK, but this is unlikely because of the fact that MAPK resides in the cytoplasm and our staining occurred in the Golgi apparatus. Also, only one of the antigen sequences, V1a, contained a sequence similar to MAPK. Even if the V1a antibody cross-reacted to MAPK, this would not explain the localization of all the other collagen XI antisera used in this study. The potential artifactual targets identified by BLAST searches are less likely targets than the intended collagen {alpha}1(XI) targets of the polyclonal antisera used in this study. We therefore conclude that we have identified collagen XI chains within normal and malignant colon tissue.

Collagen XI mRNA upregulation has been noted in the mucosa stromal cells of both familial adenomatosis polyposis and sporadic colorectal cancer, but the baseline expression and localization has not been established. Through northern blot and RT-PCR, using primers within the C1 and V1a regions and within the C-terminal domain respectively, collagen XI was not detected or perhaps was below the level of detection in normal tissue (Fischer et al. 2001aGo,bGo). The methods of Fischer et al. (2001aGo,b)Go and our study are dissimilar in that northern blot and RT-PCR detect collagen XI mRNA in the colon, whereas immunohistochemistry as carried out in our study detects collagen XI protein. Our study documents the presence of collagen XI protein in normal and malignant colon tissue using six polyclonal antisera to various locations to the exposed NTD of both the {alpha}1(XI) and {alpha}2(XI) chains.

The method and function of collagen XI's presence in the Golgi of the colonic crypt merits further study. Thyberg et al. (1979)Go suggested that the Golgi complex participated in the transfer of collagen to vesicles of the rat aorta. Conversely, collagen XI could play a role in mucus production and/or excretion. If endocytosis does occur, it might be beneficial to compare this process with disease-causing retrograde endocytosis of cholera toxin (Lencer and Tsai 2003Go; Feng et al. 2004Go) and Shiga toxin (Falguières et al. 2001Go), which both enter cells of the colon through the Golgi but are further transported into the ER. Collagen XI may be synthesized and localized to the Golgi and not further secreted or secreted normally and endocytosed back to the interior of the cell. Further studies using these antibodies will be carried out to document the transformation of the staining pattern during various stages in the development and progression of colon adenocarcinoma.


   Acknowledgments
 
This study was supported by National Institutes of Health Grants P-20RR-016454 from the IDeA Network of Biomedical Research Excellence (INBRE) Program of the National Center for Research Resources, AR-47985 (to JTO), and AR-48672 (to JTO), the Lori and Duane Stueckle professorship, and funding from the M.J. Murdock Foundation.

The authors thank Dorthyann Isaakson, Karen Halsted, Angela Modin, Raquel Brown, and Janee Mestrovich for technical support and Dr. Tom Donndelinger for light microscopy.


   Footnotes
 
Received for publication July 9, 2007; accepted November 8, 2007


   Literature Cited
Top
 Summary
 Introduction
 Materials and Methods
 Results
 Discussion
 Literature Cited
 

Bernard M, Yoshioka H, Rodriguez E, Van der Rest M, Kimura T, Ninomiya Y, Olsen BR, et al. (1988) Cloning and sequencing of pro-{alpha} 1 (XI) collagen cDNA demonstrates that type XI belongs to the fibrillar class of collagens and reveals that the expression of the gene is not restricted to cartilaginous tissue. J Biol Chem 263:17159–17166[Abstract/Free Full Text]

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