Characterization of Acetyl-CoA: Lyso-PAF Acetyltransferase of Human Mesangial Cells

Platelet activating factor (PAF) is a potent inflammatory mediator produced by various renal cells and it is implicated in renal pathology. The aim of this study is the characterization of remodeling lyso-PAF acetyltransferase, which is activated under inflammatory conditions, in human mesangial cell. Total membranes of mesangial cells were isolated and enzymatic activity and kinetic parameters were determined by trichloroacetic acid precipitation method. The effect of BSA, divalent cations, EDTA, and various chemicals on the activity of lyso-PAF acetyltransferase was also studied. Various detergents were also tested for the solubilization of the enzyme and only glycerol did not affect its activity. Partial purification of solubilized enzyme preparations of human kidney tissue and mesangial cells was performed on anion exchange column chromatography and native-PAGE electrophoresis and two active fractions were detected.


INTRODUCTION
Platelet activating factor (PAF, 1-O-alkyl-2-acetyl-snglycero-3-phosphocholine) [1] is a potent lipid mediator with a wide variety of biological activities related to physiological and pathological phenomena. Many different cells, including leukocytes, platelets, macrophages, neutrophils, lymphocytes, and endothelial cells can produce PAF under appropriate stimuli [2]. Two enzymatic pathways of PAF biosynthesis have been described [3]. The de novo pathway entails a specific stepwise sequence of reactions starting with the acetylation of 1-O-alkyl-snglycero-3-phosphate, which is an ether-linked metabolic intermediate formed soon after the ether bond is created. In contrast, the remodeling pathway involves a structural modification of preexisting ether-linked phospholipids that serve as structural components of membranes [3]. It is believed that the remodeling route plays a crucial role in inflammatory/hypersensitivity responses of cells whereas the de novo reaction sequence appears to be of physiological importance maintaining basal PAF levels in various tissues and blood. The main enzyme for PAF degradation is PAF-acetylhydrolase (PAF-AH) [4].
PAF in the kidney can be produced by both biosynthetic routes either by infiltrating inflammatory cells or Correspondence and reprint requests to Constantinos Alexandros Demopoulos, Faculty of Chemistry, National and Kapodistrian University of Athens, Panepistimioupolis, 15771 Athens, Greece; demopoulos@chem.uoa.gr by intrinsic glomerular cells such as mesangial cells [5]. Mesangial cells account for 20%-25% of all glomerular cells. They are localized in the centre of the glomerular tuft and they have very important physiological functions including structural support of capillary net work, participation in filtration regulation, synthesis and secretion of matrix, eicosanoids, growth factors, and cytokines [6]. These cells are influenced by both autocrine and paracrine activities of the above factors. Apart from its physiological effects, the PAF produced in kidney is involved in the pathogenesis of renal damage [7,8,9]. PAF infusion into the renal artery of animals reduces the glomerular filtration rate and the renal blood flow, and increases proteinuria and glomerular permeability [9]. Moreover, increased levels of PAF and PAF-like lipids have been detected in experimental models of glomerulonephritis while parallel administration of PAF antagonists prevented or reduced renal damage [10]. In vitro experiments revealed that PAF has multiple actions in glomerular cells, especially in mesangial cells since it stimulates several signalling pathways [11], causes contraction [5] and matrix production [12]. These observations are supported by a limited number of clinical studies demonstrating increased PAF in patients with primary glomerulonephritis [13], IgA nephropathy [14], and membranous nephropathy [15].
The study of the enzymes of PAF metabolism is of great interest since they regulate PAF levels both intracellularly and extracellularly. Many of the features of progressive glomerular diseases share common biological mechanisms with those of atherosclerosis. Among them, inflammation is dominant. The last step in the remodeling pathway, which is activated under inflammatory conditions, is catalysed by the enzyme acetyl-CoA:1-O-alkyl-sn-glycero-3-phosphocholine acetyltransferase (lyso-PAF AT) (EC 2.3.1.67) which transfers an acetyl group in the sn-2 position of lyso-PAF. Lyso-PAF AT occurs in the microsomal fraction of a variety of tissues [16] and blood cells [17,18]. The substrate specificity of the lyso-PAF AT is rather broad since 1-acyl-2-lysoglycerophosphocholine, 1-alky-1enyl-2lysoglycerophosphoethanolamine, and other analogues serve as substrates. Similarly, short-chain acyl-CoAs (C2-C6) can be used as substrates for the acetyltransferase [19]. Calcium has been reported to be necessary for the expression of lyso-PAF AT activity although contrasting evidence has been found [16,20,21]. Partial purification of the enzyme from rat spleen has been reported. Electrophoresis of the partially purified enzyme after the incorporation of labelled PAF revealed that the radioactivity was associated with a protein possessing a molecular mass of 29 kd [22]. No subsequent experiments with purified preparations of the enzyme have been described, although solubilization of the enzyme with glycerol has been reported [23]. Lyso-PAF AT seems to be activated/inactivated by a phosphorylation/dephosphorylation mechanism [24,25,26,27,28,29]. AMP-dependent protein kinase, calcium calmodulindependent protein kinase, protein kinase C, and kinase p38 seem to be involved in the phosphorylation of the enzyme.
PAF-AH as well as remodeling and de novo acetyltransferases have been previously characterized in cortex and medulla from human kidney tissue by our laboratory [20,30,31]. Although PAF metabolism has been described in mesangial cells [32,33], as far as we know there are no direct studies on PAF biosynthetic enzymes. In the present study, remodeling lyso-PAF AT was identified and characterized in human mesangial cell line while a partial purification on lyso-PAF AT from human kidney tissue and human mesangial cells is reported.

Materials and instrumentation
All centrifugations were performed in a Sorvall RC-5B refrigerated superspeed centrifuge (Sigma) apart from the centrifugation at 100 000 xg, which was performed in a Heraeus-Christ, Omega 70000 ultracentrifuge (Hanau, Germany). For the precipitation of the bovine serum albumin (BSA) pellet, a Sigma 201 M microcentrifuge was used (Sigma, Saint Louis, Mo, USA). The separation of protein was performed at 4 • C on an HP HPLC Series 1100 liquid chromatography model (Hewlett Packard, Waldbronn, German) equipped with a 100 µL Rheodyne (7725 i) loop valve injector, a degasser G1322A, a quat gradient pump G1311A, and an HP UV spectrophotometer G1314A as a detection system. The spectrophotometer was connected to a Hewlett-Packard (Hewlett Packard, Waldbronn, German) model HP-3395 integrator-plotter. An anion exchange column has been used for the separation of proteins (Resource Q, Amersham-Pharmacia Biotech AB).
Radioactivity was measured in a 1209 Rack Beta flexivial liquid scintillation counter (Pharmacia).

Human kidney tissues
Human kidney tissues were obtained from nephrectomized patients with adenocarcinoma. Immediately after the nephrectomy, the kidneys were perfused with normal saline and a speciment obtained of the apparently normal parenchyma and placed immediately in cold saline. Subsequently, all homogenization and subcellular fractionation procedures were completed in less than 3 hours.

Homogenisation of kidney tissues and preparation of subcellular fractions
Homogenisation of mesangial cells or kidney samples and preparation of subcellular fraction was carried out by a modification [20] of the method described by Lenihan and Lee [25]. Briefly, mesangial cells were cultured in 75 cm 2 flasks, the pellet of the cells was resuspended in homogenisation buffer containing 0.25 M sucrose, 10 mM EDTA, 5 mM mercaptoethanol (MeEtOH), 50 mM NaF, 50 mM Tris-HCl (pH 7.4), and were homogenized by sonication.
Kidney tissues were rinsed with ice-cold 0.25 M sucrose, then minced and homogenized with six strokes of a motor-driven Potter-Elvehjem homogeniser in homogenisation buffer. The final concentration of the tissue in the homogenisation buffer was 10% w/v. Further homogenisation of the tissue by sonication was followed. In both cases, the homogenates were centrifuged at 500 xg for 10 minutes. The pellets were discarded, a small portion of the supernatants was kept for protein and lyso-PAF AT determination and the rest of them were centrifuged at 100 000 xg for 1 hour. The resulting pellets, total membranes (TM), were suspended in suspension buffer containing 0.25 M sucrose, 1 mM DTT, 50 mM Tris-HCl (pH 7.4) (5-10 mg of protein/mL). All fractions were aliquoted and stored at −20 • C. All homogenization and fractionation procedures were taken place at 4 • C.

Lyso-PAF AT activity assay
Lyso-PAF AT activity was measured by the method of trichloroacetic acid (TCA) previously described [20]. Unless stated otherwise, subcellular fractions of mesangial cells or kidney tissue, containing 10-50 µg of total protein, were incubated with 20 µM of lyso-PAF and 200 µM of [H 3 ]-acetyl-CoA (100 Bq/nmoL) for 30 minutes at 37 • C in a final volume of 200 µL of 50 mM Tris-HCl buffer (pH 7.4) containing 0.25 mg/mL BSA. By the end of the incubation time 0.2 mg of BSA were added and the reaction was stopped by the addition of cold TCA solution 9.6% final concentration. The reaction mixture was kept in ice for 30 minutes and centrifuged at 10 000 xg for 2 minutes. The supernatant was discarded and the pellet containing the [H 3 ]PAF bound to the denaturated BSA is dissolved in the scintillation cocktail (dioxane-base) and the radioactivity was determined by liquid scintillation counting. Matching controls were run in the absence of lyso-PAF in order to subtract the radioactivity of the endogenously produced [H 3 ]PAF.

Solubilization of proteins
For the solubilization of the proteins, total membranes fractions were suspended in Tris-HCl buffer pH 7.4 with different detergents in various concentrations (w.v.) and various ratios of detergent/protein (w.w.). The mixture was kept in ice for 40 minutes and it was centrifuged at 100 000 xg for 1 hour at 4 • C. The pellets were resuspended in suspension buffer. Both supernatants and resuspends pellets were tested for lyso-PAF AT activity and their protein concentration was determined.

HPLC separation
Supernatants were placed in two-compartment centrifuge tubes containing membranes with cutoff value of 10 000 Da and concentrated by centrifugation at 5000 xg for 5 hours at 4 • C. The remaining concentrates were resuspended in Tris-HCl pH 7.4 and centrifuged at 5000 xg for 2 hours at 4 • C for the removal of the excess glycerol. The total volume of the sample after centrifugation was 50-200 µL. The separation was carried out on an anion exchange column. The elution system consisted of a linear gradient from, starting buffer containing 20 mM Tris-HCl pH 8.0 to elution buffer containing 20 mM Tris-HCl and 0.5 M KCl pH 8.0 in 25 minutes. The flow rate was 0.8 mL/min and UV detection was carried out at 280 nm. One-minute fractions were collected for 30 minutes.

ELECTROPHORESIS
Nondenaturing electrophoresis was carried out by a method previously described by Laemmli [35], in which SDS was replaced by the nondenaturing 3-[(3-cholamidopropyl)-dimethylammonio]-1-propanesulfonate (CHAPS) (10 mM). Slab gels consisting of 12% (w.v.) separating polyacrilamide gel in 1.5 M Tris-HCl, pH 8.8 were exposed to a constant 30 mA (250 V) for 4.5 hours at 4 • C. The stacking gel was made up as a 4% (w.v.) gel in 0.5 M Tris-HCl pH 6.5. The pH of the electrophoresis buffer was 8.3. The samples were run in duplicate. Upon completion of electrophoresis, the gel was divided into two parts. The first part was sliced into 0.4 cm horizontal strips, which were individually extracted with 0.5 ml Tris-HCl pH 7.4, incubated, overnight at 4 • C and collected by centrifugation. The second part was stained by Coomassie Blue. Molecular markers (phosphatase-β 97.4 kd, bovine serum albumin 66.2 kd, ovalbumin 45 kd, carbonic anhydrolase 31 kd, trypsin inhibitor 21.5 kd) were run in parallel with the samples.

Analytical methods
Protein was determined by the method of Bradford [36].

Statistical analysis
Unless otherwise stated, data are expressed as mean values ± SD. The linear or nonlinear regressions of enzymes kinetics were made using GraphPad Prism. In order to compare the influence of several factors on enzyme activity, t test for independent samples was performed on the specific activities values. All analyses were done with the Statistical Package for Social Sciences (SPSS, version 10.0, SPSS Inc, Chicago, Ill, USA). Differences were considered statistically significant at the 5% level.

Lyso-PAF AT activity of HMC and human kidney tissues
The specific activity of lyso-PAF AT was measured in 500 xg (homogenate fractions) and 100 000 xg (cytoplasmic fractions) supernatants as well as at 100 000 xg pellets (total membrane fractions) of mesangial cells or human kidney tissue preparations. The results are shown in Table  1. Lyso-PAF AT activity was detected in the 100 000 xg pellet. Heating of samples at 50 • C and 60 • C for 10 minutes resulted in 85% and 100% inactivation of the existing enzyme activity, respectively. Lyso-PAF AT specific activity was reduced 40% after a 20-day storage at −20 • C. All subsequent experiments were performed with total membrane (TM) preparations.

Effect of temperature and pH on lyso-PAF AT activity of HMC
Experiments were carried out in order to found the optimum conditions for the action of the enzyme. The temperature-activity profile was bell-shaped showing an optimum at 37 • C. Three different buffer solutions of various pH values, namely, 50 mM acetic buffer pH 4-6, 50 mM phosphate buffer pH 6-7, and Tris-HCl buffer pH 7-9, were utilized in order to investigate the dependence of lyso-PAF AT activity on pH. The results are shown in Figure 1. Lyso-PAF AT showed maximum activity at a pH range between 7.2 and 7.4.

Effect of BSA on lyso-PAF AT activity of HMC
The effect of BSA concentration on the activity of total membrane fractions of lyso-PAF AT was studied. As shown in Figure 2, the maximum enzyme activity occurred at 0.25 mg/mL BSA final concentration in reaction mixture while 2.0 mg/mL BSA reduced the activity by 15% compared to the non-added control. The t test for independent samples revealed that only 0.25 mg/ml concentration of BSA gave statistical significance difference from the non-added control value (P = .049). Therefore, 0.25 mg/mL final concentration BSA was routinely used.

Dependence of PAF formation by protein concentration and incubation time
The kinetics of PAF formation in relation to time and the dependence of TM lyso-PAF AT activity on protein concentration are shown in Figure 3. The total amount of PAF formed at the end of each incubation time decreased as protein concentration decreased (Figure 3a). A linear relationship between the initial velocity and total protein up to 0.05 mg (0.25 mg/mL) was found for 30-minute incubation time (Figure 3b). In order to achieve the maximum yield of reaction 0.02-0.05 mg (0.1-0.25 mg/mL) protein and 30-minute incubation time were routinely used.

Effect of substrates concentration on lyso-PAF AT activity and kinetic parameters
The activity of lyso-PAF AT was determined at different acetyl-CoA concentrations ranging from 25 to 800 µM at a fixed concentration of lyso-PAF 20 µM. The results revealed that enzyme exhibited classical Michaelis-Menten kinetics with respect to acetyl-CoA. When the concentration of lyso-PAF was varied between 2.5 and 100 µM at a fixed concentration of acetyl-CoA (200 µM), the enzyme followed simple saturation kinetics only up to 40 µM.  Higher concentrations of lyso-PAF resulted in a drop of enzyme activity that was consistent with previously published data [20,27]. The kinetic parameters of the enzyme revealed from these experiments are summarized in Table 2. The calculations for acetyl-CoA were made using nonlinear regression while the calculations for lyso-PAF were made using linear regression (Lineweaver-Burk plot) since there was no classical saturation curve.

Effect of divalent cations on lyso-PAF AT activity of HMC
In order to study the effect of divalent cations (Ca 2+ and Mg 2+ ) on the activity of lyso-PAF AT, 0.15 mg/mL of TM were incubated in the presence of various concentrations of CaCl 2 and MgCl 2 . Low concentrations  Figure 4. Initial velocity data were analyzed by weighted fits to the Michaelis-Menten equation using linear regression for up to 40 µM lyso-PAF from GraphPad Prism. b Kinetic data were obtained from experiments shown in Figure 4.
Initial velocity data were analyzed by weighted fits to the Mechaelis-Menten equation using nonlinear regression programme adapted from GraphPad Prism. 10 −5 -10 −3 M of Ca 2+ and Mg 2+ did not influence the activity of lyso-PAF AT while at higher concentration Ca 2+ and Mg 2+ (10 −2 M) significantly (P < .05) reduced lyso-PAF AT activity by 46 and 19%, respectively. When TM were incubated in the presence of ethylene-diamino-tetraacetic acid (EDTA) 10 −3 M the enzyme activity was significantly (P < .05) reduced by 47% while the addition of Ca 2+ 10 −2 M partially overrode this reduction (P = .097) ( Table 3).

EFFECT OF CHEMICALS ON LYSO-PAF AT ACTIVITY OF HMC
The effect of various chemicals on lyso-PAF AT activity was also studied. The results are summarized in Figure  5. Sulfonyl-type serine protease inhibitors like Pefabloc did not influence the activity of lyso-PAF AT. The protease inhibitor NaF (sodium fluoride) slightly increases  Experiments were performed at total membrane fractions using 0.23 mg/mL protein in optimum conditions. Results represent the average ± SD from four independent determinations using different enzyme preparations performing duplicate samples. the activity of the enzyme. Dithiothreitol (DTT) inhibited enzyme activity with a dose-dependent manner. Since DTT reduces disulfide bridges present in polypeptides and proteins, this result indicates the presence of disulfide bridges in the enzyme. Moreover, mercaptoethanol had the same action with DTT supporting the existence of disulfide groups ( Figure 5). The t test for independent samples revealed that only DTT at 5 mM and mercaptoethanol reduced significant the activity of the enzyme with P values .000 and .035, respectively.

Solubilization of total membranes
An essential step in purifying the membrane enzyme is to solubilize the enzyme from the membranes. For this purpose, total membrane fractions from human kidney tissue were used. All attempts to solubilize total membrane fractions by sonication, in the absence of detergents, were unsuccessful, therefore total membranes were incubated with various solubilizing agents. Lyso-PAF AT activity and the protein concentration were measured in the supernatants and the pellets. A control in absence of detergent was run concomitantly and the values were expressed as the % specific activity of lyso-PAF AT in the supernatants of the solubilization procedure compared to the non-added control (% non-added control). We tried the ionic detergent sodium deoxycholate (0. . Although all detergents were successfully solubilized protein, glycerol was the only detergent able to solubilize the enzyme without inactivating it. As shown in Table 4, the higher the glycerol concentration, the more effective the enzyme solubilization. Therefore, routine solubilization of TM fractions from human kidney tissue and HMC was carried out with 30% w.w. glycerol (glycerol/protein 167 w.w.) for routine process. Higher glycerol concentration made the removal of it difficult in the next steps of purification. The kinetics parameters of the solubilized fractions from HMC were also studied. These experiments revealed K M, app and Vmax,app values of TM and solubilized fractions 51.2 µM, 2.96 nmol/min/mg and 42.0 µM, 2.05 nmol/min/mg, respectively, with respect to acetyl-CoA and 11.3 µM, 3.17 nmol/min/mg and 12.4 µM, 2.86 nmol/min/mg, respectively, with respect to lyso-PAF.
Ion exchange chromatography -HPLC In order to perform chromatographic separation, the solubilized enzyme fractions had to be concentrated. All attempts made to lyophilize the solubilized fractions  resulted in enzyme inactivation, for this reason, ultrafiltration using two compartment centrifuge tubes was carried out as described in methods. The solubilized concentrated fractions of human kidney tissue and HMC were subjected to HPLC separation under the conditions described in methods. Lyso-PAF AT activity of human kidney tissue was recovered in fractions 1, 2-4, and 10-15 while the respective activity of the HMC in fractions 1-3 ( Figure 6). The apparent K M ,app and Vmax,app values with respect to lyso-PAF AT of HPLC active fractions from HMC were 19.2 µM, 2.52 nmol/min/mg. The yield of this step was 10.2 and purification 1.6.

Nondenaturing electrophoresis
The solubilized fraction from human kidney tissue, since there was not enough amount after the HPLC separation, and the active HPLC fractions 1-2 from mesangial cells were subjected to gel-electrophoresis according to methods. The activity of the lyso-PAF AT was present in two gel fragments corresponding to apparent molecular weight values of 25-30 kd of human kidney tissue, 75-85 kd of human kidney tissue, and 25-30 kd and 65-80 kd of HMC (Figure 7). The calculation of apparent molecular weight was made based on the log MW = f (R f ) function, which under the electrophoresis conditions was linear (y = −1.045x + 4.97, R 2 = 0.9875). The enzyme specific activity of the active fragment (25-30 kd) of HMC after nondenature PAGE was 2.78 nmol/min/mg. The yield of this step was 0.01 and purification 1.9.

DISCUSSION
Platelet activating factor is a potent phospholipid mediator that is produced by a variety of tissues and cells [1,2]. The balance between PAF biosynthesis and degradation determines its levels. De novo biosynthesis pathway is thought to be responsible for the resting state levels of PAF while the remodeling pathway is thought to play a crucial role in inflammatory responses. Degradation of PAF occurs mainly with PAF-AH, which converts it to inactive lyso-PAF. Although many studies exist for PAF-AH, which has been cloned, there are not many studies about biosynthetic enzymes of PAF metabolism. Lyso-PAF AT is the main enzyme in remodeling pathway and converts lyso-PAF to PAF using acetyl-CoA as acetyl donor.
We have previously detected and characterized lyso-PAF AT activity in cortex and medulla of human kidney tissue [20]. In this study, we detected and characterized lyso-PAF AT in human mesangial cells. Mesangial cells are the main source of PAF in kidney and as far as we know there is no any study on lyso-PAF AT in mesangial cells.
As previously described from others and us, the activity of lyso-PAF AT has been detected on mitochondria and microsomal fractions [20,21,27]. In order to have the maximum enzyme amount, total membranes fractions were used for the process. Total membranes lyso-PAF activity was abolished when samples were pre-incubated at 60 • C for 10 minutes. Maximum lyso-PAF AT activity was obtained at pH 7.4 and at incubation temperature 37 • C while dependence of enzyme activity on total protein showed linearity up to 50 µg (250 µg/mL). Assays of acetyltransferase with lyso-PAF as a substrate are routinely performed in the presence of BSA, which binds PAF as it is formed [34]. It has been reported that 0.75-2.5 mg/mL BSA in the presence of low protein concentration (10-60 µg/mL) activates lyso-PAF AT while higher protein concentration (200 µg/mL) showed no significant effect. In the present study 230 µg/mL of protein was used and BSA significantly increased (P < .05) the activity of lyso-PAF AT at 0.25 mg/mL while at higher concentration caused a slightly not significant reduction of lyso-PAF AT activity. This result is with agreement with previous report that demonstrating that the membranes could be also effective in binding PAF [32].
Regarding the effect of substrates on lyso-PAF AT activity the experiments revealed that lyso-PAF AT followed typical Michaelis-Menten kinetic profile with respect to acetyl-CoA while followed simple saturation kinetics with respect to lyso-PAF only up to 50 µM. Higher concentrations of lyso-PAF resulted in a drop of enzyme activity. This is consistent with previous data from our laboratory and others and probably due to detergent effect of lysophospholipids [20,37].
Exogenous addition of the divalent cations Ca 2+ and Mg 2+ (10 −2 M) at high concentrations reduced the enzyme activity. EDTA inhibited the lyso-PAF AT activity and this inhibition is partially reversed by the addition of Ca 2+ . It seems that lyso-PAF AT required a specific concentration of Ca +2 for its activation and that higher or lower concentration resulting in inactivation. It has been reported that Ca 2+ is required for the lyso-PAF activity [20,38] but others have been indicated otherwise [16].
DTT and mercaptoethanol significantly (P < .000 and P < .05, respectively) inhibited lyso-PAF acetyltranserase indicating that there are disulfide bridges present in the enzyme. Pefabloc had no significant effect on the enzyme action supporting the absence of serine(s) in the active site of the enzyme. In addition, pefabloc is a PAF AH inhibitor and it seems that the possible presence of PAF AH in the assay did not influence PAF formation, which is in agreement with our previous results [20].
Lyso-PAF AT is a very labile enzyme that is very sensitive to detergents. Solubilization of the enzyme from other tissues with sodium deoxycholate and glycerol has already been reported [22,23,24]. In the present study, most of the common detergents used resulted in total inactivation of the enzyme and only glycerol managed to solubilize the enzyme without inactivation. Concentration of 32% w.w glycerol had a 24% yield in the solubilization of human kidney tissue and human mesangial cells lyso-PAF AT. Furthermore, an attempt was made to purify lyso-PAF AT from human kidney tissue and human mesangial cells. The partial purification procedure consisted of only two steps, namely, anion exchange chromatography and native-PAGE electophoresis, since the limited amount of enzyme preparation along with the low recovery rate, especially in human kidney tissues, prevented us from utilizing a more extensive purification process. Native-PAGE electrophoresis of the partially purified enzyme from human kidney tissue and HMC resulted in two active fractions in both cases of approximately 25-30 kd and 75-85 kd molecular weight. A 30 kd band of lyso-PAF AT activity from rat spleens after nondenaturing conditions electrophoresis has been reported [24]. More investigation is required in order to explain if the one band is due to an enzyme dimmer formation or to another isoenzyme or more possible to an enzyme comlex with membrane fractions.
These data demonstrate that lyso-PAF acetyltranferase activity is present in human mesangial cells and established the biochemical properties of this enzyme for the first time in human mesangial cells. Concerning our previous data, lyso-PAF AT of mesangial cells seems to have similar properties with lyso-PAF AT characterized in human kidney tissue (medulla and cortex), supporting that mesangial cells are the primary source of PAF in the kidney. Moreover, solubilization and partial purification of human kidney tissue and mesangial cells lyso-PAF AT were achieved.
PAF production in kidney, mainly by mesangial cells, is involved in the pathogenesis of renal damage. The characterization of lyso-PAF AT activity in human mesangial cells enables the further investigation of lyso-PAF AT regulatory mechanisms and therefore PAF production under inflammatory conditions.