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The plasma membrane carbonic anhydrase in murine hepatocytes identified as isozyme XIV
© Parkkila et al; licensee BioMed Central Ltd. 2002
Received: 22 April 2002
Accepted: 21 May 2002
Published: 21 May 2002
Biochemical and histochemical studies have both previously indicated plasma membrane-associated carbonic anhydrase (CA) activity in hepatocytes which has been assumed to be CA IV. However, immunohistochemical data did not support this assignment. Recent northern blotting results indicated the presence of mRNA for the most recently discovered membrane-bound CA isozyme, CA XIV, in the liver. The present study was designed to examine whether CA XIV could contribute to the CA activity described in the hepatocytes.
Tissue samples from mouse liver were subjected to immunohistochemical staining using the antibodies raised against recombinant mouse CA XIV and CA IV. RT-PCR and western blotting were also performed for CA XIV.
A strong immunofluorescent signal was observed in the plasma membrane of mouse hepatocytes. Although CA XIV was expressed on both the apical and basolateral surfaces, the staining was more prominent at the apical (canalicular) membrane domain. The expression of CA XIV in the liver was confirmed by RT-PCR and western blotting.
The presence of CA XIV in the hepatocyte plasma membrane places this novel enzyme at a strategic site to control pH regulation and ion transport between the hepatocytes, sinusoids and bile canaliculi.
Carbonic anhydrases (CAs) are produced in a variety of tissues where they participate in a broad range of physiological processes such as acid-base homeostasis, carbon dioxide and ion transport, respiration, bone resorption, renal acidification, gluconeogenesis, ureagenesis, and formation of cerebrospinal fluid and gastric acid . The expanding α-CA gene family includes 11 enzymatically active members with different structural and catalytic properties. The cellular distribution and physiological functions of the various CA isozymes have been extensively described in several recent reviews [1–4]. The most recently characterized isozyme is CA XIV, the mRNA of which has been demonstrated in the brain, kidney, liver, skeletal muscle, heart, and lung [5, 6]. By immunohistochemistry, CA XIV showed a unique distribution in neurons of mammalian brain, and was expressed particularly strongly in neurons involved in motor function and coordination . These observations made CA XIV a likely candidate for the extracellular CA postulated to have an important role in modulating excitatory synaptic transmission in brain.
In a more recent study, CA XIV was demonstrated in renal tubule cells . Immunofluorescence staining showed strong signal for CA XIV in the apical plasma membrane of the S1 and S2 segments of proximal tubules. The staining was weaker in the basolateral membrane of these tubules. In addition, strong staining was seen in the initial portion of the thin descending limb of Henle. The results suggested that CA XIV probably accounts for a substantial fraction of the bicarbonate reabsorption in the kidney.
The present study was designed to examine the cellular localization of CA XIV in the liver which has previously shown CA XIV mRNA expression in northern blots [5, 6]. By histochemical staining, hepatocytes have exhibited plasma membrane-associated CA activity . Moderate membrane-associated staining was reported in the hepatocytes surrounding the portal spaces, and the staining weakened towards the central vein. Prior to discovery of additional membrane-associated CAs, the CA activity in hepatocytes was assumed to be due to CA IV. However, recent immunohistochemical data failed to support this assignment . The present results demonstrate the expression of CA XIV at the hepatocyte plasma membrane, suggesting a key role for this isozyme in the regulation of ion and pH homeostasis in parenchymal cells of the liver.
Materials and Methods
The rabbit anti-mouse CA XIV antiserum to the secretory form of mouse CA XIV was raised in rabbits as described recently by Parkkila et al. . The rabbit anti-mouse CA IV and rabbit anti-rat CA II antisera have also been described earlier [11, 12]. All secondary antibodies used in immunofluorescence were purchased from Molecular Probes (Eugene, OR).
Adult male mice (Balb/c) were sacrificed by decapitation. The abdominal organs were perfused in situ through the abdominal aorta with 3% paraformaldehyde in phosphate-buffered saline (PBS), removed, and cut into slices. The slices were further immersion-fixed in 3% paraformaldehyde for 2 h at room temperature, cryoprotected overnight in 20% sucrose-PBS, and rapidly frozen in liquid nitrogen-cooled isopentane. Sections were cut at 5 μm using a Microm Cryo-Star microtome (Microm, Walldorf, Germany), dried onto Superfrost Plus microscope slides (Menzel, Braunschweig, Germany), and incubated with PBS containing 20% cow colostral whey for 40 min. The sections were then incubated for 2 h with polyclonal anti-CA XIV or preimmune serum, diluted 1:200 in 1% bovine serum albumin (BSA)-PBS, washed three times for 5 min in PBS and incubated for 1 h with Alexa 568-coupled goat anti-rabbit IgG, diluted 1:200 in BSA-PBS. After four 5-min washes in PBS, slides were mounted in Immu-mount (Shandon, Pittsburgh, PA). The sections were examined with a conventional epifluorescence microscope (Nikon Corporation, Tokyo, Japan) or a confocal laser-scanning microscope (Zeiss, Göttingen, Germany).
Mice were sacrificed by decapitation, and the liver and colon were removed. 20 μg of total cell protein per lane from homogenized tissue samples or stably transfected CHO cells expressing wild-type mouse CA XIV  was subjected to SDS-PAGE under reducing conditions according to Laemmli . Protein standards for SDS-PAGE were from Bio-Rad Laboratories (Richmond, CA). The electrophoreses were performed in a Novex XCell SureLock electrophoresis unit (Invitrogen Corp/NOVEX, Carlsbad, CA) using a Novex NuPAGE 10% Bis-Tris gels. The proteins were transferred electrophoretically from the gel to a nylon membrane (Millipore; Bedford, MA) in a Novex Blot Module. After the transblotting the membrane was first incubated with TBST buffer (10 mM Tris-HCl, pH 7.5, 150 mM NaCl, 0.05% Tween-20) containing 10% cow colostral whey (BioTop, Oulu, Finland) for 25 min at 4°C, and then with anti-mouse CA XIV serum or anti-rat CA II serum diluted 1:2000 in TBST buffer for 1 h at room temperature. The sheets were washed four times for 5 min with TBST buffer and incubated for 30 min at room temperature with alkaline phosphatase-conjugated goat anti-rabbit IgG (Bio-Rad Laboratories) diluted 1:3000 in TBST buffer. After washing three times for 5 min in TBST buffer, the polypeptides were visualized by a chemiluminescence substrate (Bio-Rad Laboratories).
Extraction of RNA and Reverse Transcription-Polymerase Chain Reaction (RT-PCR)
The liver, colon, jejunum, and kidneys were removed from mice and the samples were used for RT-PCR analysis. Epithelial cells of the intestinal mucosa were obtained by using a scraping technique as described . The mucosa from a fresh tissue sample was gently scraped using the short edge of a microscope slide. The scrapings were quickly transferred to a microtube and frozen in liquid nitrogen. Total cellular RNA was extracted from the cell or tissue samples using TRIzol reagent (Gibco-BRL, Gaithersburg, MD), according to the manufacturer's instructions. The concentration and purity of RNA was determined by spectrophotometer at 260 and 280 nm. Reverse transcription (RT) and polymerase chain reaction (PCR) amplification were performed using a single-step method . Two primers for amplifying CA XIV were chosen based on the published mouse CA XIV sequence ; forward 5'-AAGGTGACTTGGATCCTGGCTGCA-3' (nucleotides 290–313) and reverse 5'-TTCTGAGCTGCCTCACTCAAGCTG-3' (nucleotides 700–723), which generated a 434-bp amplification product. Primers for rat glyceraldehyde-6-phosphate (GAPDH)  were used to monitor the quality of the RNA samples.
Ten micrograms of total RNA was used as a template for subsequent RT and PCR reactions. Reverse transcription was performed at 42°C for 1 hour followed by denaturation at 95°C for 2 minutes. The PCR cycling protocol consisted of 30 cycles of denaturation at 95°C for 1 minute, annealing at 55°C for 1 minute, and extension at 72°C for 1 minute, followed by final extension at 72°C for 5 minutes. The PCR products were analyzed by electrophoresis on 1.5% agarose gels containing ethidium bromide.
Western blotting and RT-PCR
Based on the previous and present data hepatocytes express at least four CA isozymes. Two of them are cytosolic, namely CAs II and III. The function of the high activity isozyme, CA II, has been linked to the intracellular hydration of carbon dioxide and alkalization of hepatic bile . Based on the studies with CA III-overexpressing cells and on the expression profile of CA III in alcoholic liver, it has been proposed to participate in free radical scavenging systems [18, 19]. Mitochondrial CA VA plays a key role in gluconeogenesis and ureagenesis in the liver, where bicarbonate is required as a substrate to two enzymes, pyruvate carboxylase and carbamyl phosphate synthetase .
In a previous report, we have shown that CA IV, which is anchored to the plasma membrane by glycosyl phosphatidylinositol linkage, is located in the human biliary epithelial cells, but is absent in the human hepatocytes . Here, we demonstrated that CA IV is expressed in the sinusoid lining cells of the mouse liver, while no staining was seen in the hepatocyte plasma membrane. Based on these observations, we conclude that CA XIV is the membrane-associated CA isozyme identified in the hepatocytes by histochemical studies. One discrepancy still remains in that the present results showed no zonal variation in the staining intensity, whereas Ridderstråle et al.  reported that the histochemical staining decreased towards the central vein. The exact reason for this difference is not known. It should be noted, however, that Ridderstråle et al.  used CA II-deficient mice in the analyses, and the gene defect could potentially change the expression and distribution pattern of other CAs.
The plasma membrane-associated CA activity in hepatocytes was originally demonstrated by Garcia-Marín et al.  using a biochemical method and by Ono et al.  using a histochemical cobalt precipitation technique. At the same time, information on different ion transport proteins in hepatocyte plasma membrane accumulated that linked the plasma membrane-bound CA activity to ion transport mechanisms. Blitzer and Boyer  had earlier demonstrated the localization of Na+,K+-ATPase at the basolateral plasma membrane. Henderson et al.  and Renner et al.  showed that Na+/H+-exchanger regulates intracellular pH in isolated hepatocytes. Soon after these discoveries, Gleeson et al.  and Benedetti et al.  demonstrated that a Na+-HCO3 - cotransporter and Cl--HCO3 - exchanger are important regulators of intracellular pH, in addition to the Na+/H+ exchanger. The Na+/H+ exchanger most probably participates in acid extrusion . The Na+/HCO3 - cotransporter has been implicated in Na+ and HCO3 - reabsorption . The Cl-/HCO3 - exchanger most probably plays a role in recovery from intracellular alkalization by removing HCO3 - from the cytoplasm . CA XIV, as a membrane-bound isozyme with its active site on the cell exterior, is a good candidate to participate in regulation of pH homeostasis and ion transport between the hepatocytes, bile canaliculi and hepatic sinusoids.
Although CA IV is not expressed on hepatic plasma membranes, where CA XIV is strongly expressed, CA IV is expressed in the sinusoid lining cells, where CA XIV is weakly expressed. Here both isozymes may participate in ion transport and pH homeostasis across the plasma face of the sinusoidal endothelial cells. CA IV is similarly expressed on the plasma face of pulmonary microcapillaries  and cortical capillaries in brain , both areas where CO2 flux is high.
It is likely that the membrane-associated CAs in liver appear with differentiation of the hepatocytes. Garcia-Marin et al.  observed that membrane-bound CA activity correlates with hepatic regeneration following partial hepatectomy. They measured CA activity in both soluble and plasma membrane-enriched fractions obtained from liver homogenate from rats undergoing hepatectomy. They found no changes in CA activity in the soluble fraction. However, the CA activity in plasma membrane was reduced by 55% soon after hepatectomy and returned to near control value at seven days. It would be of interest to determine the relevant contributions of CA XIV and CA IV to this increase in expression during the regenerative process, and whether the regeneration of the differentiated phenotype is dependent upon expression of the CAs. Testing hepatic regenerative capacity should be included in the physiological studies characterizing CA XIV and CA IV deficient mice when suitable knock-out animal models become available.
The present paper demonstrates for the first time the expression of CA XIV at the hepatocyte plasma membrane. Its localization on both apical and basolateral membrane domains suggests an important role for this isozyme in the regulation of ion and pH homeostasis in the liver.
The authors thank Ms. Sirpa Kellokumpu and Ms. Lissu Hukkanen for technical assistance. The study has been supported by a grant from Sigrid Juselius Foundation to SP and grants DK40163, GM34182, and GM53405 from the National Institutes of Health to WSS.
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