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Braz J Med Biol Res vol.34 no.8 Ribeirão Preto Aug. 2001
Braz J Med Biol Res, August 2001, Volume 34(8) 985-991
a-Smooth muscle actin and proliferating cell nuclear antigen expression in focal segmental glomerulosclerosis: functional and structural parameters of renal disease progression
Departamentos de 1Clínica Médica, 2Patologia, and 3Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil
Subjects and Methods
Correspondence and Footnotes
The aim of the present study was to investigate the expression of a-smooth muscle actin (a-SM-actin) and proliferating cell nuclear antigen (PCNA) in renal cortex from patients with focal segmental glomerulosclerosis (FSGS) and their correlations with parameters of renal disease progression. We analyzed renal biopsies from 41 patients with idiopathic FSGS and from 14 control individuals. The a-SM-actin immunoreaction was evaluated using a score that reflected the changes in the extent and intensity of staining in the glomerular or cortical area. The PCNA reaction was quantified by counting the labeled cells of the glomeruli or renal cortex. The results, reported as median ± percentile (25th; 75th), showed that the a-SM-actin scores in the glomeruli and tubulointerstitium from the renal cortex were 2.0 (2.0; 4.0) and 3.0 (3.0; 4.0), respectively, in patients with FSGS, and 0.5 (0.0; 1.0) and 0.0 (0.0; 0.5) in the controls. The number of PCNA-positive cells per glomerulus and graded field of tubulointerstitium from the renal cortex was 0.2 (0.0; 0.4) and 1.1 (0.3; 2.2), respectively, for patients with FSGS, and 0.0 (0.0; 0.5) and 0.0 (0.0; 0.0) for controls. The present data showed an increase of a-SM-actin and PCNA expression in glomeruli and renal cortex from FSGS patients. The extent of immunoreaction for a-SM-actin in the tubulointerstitial area was correlated with the intensity of proteinuria. However, there was no correlation between the kidney expression of these proteins and the reciprocal of plasma creatinine level or renal fibrosis. These findings suggest that the immunohistochemical alterations may be reversible.
Key words: a-smooth muscle actin, proliferating cell nuclear antigen, PCNA, focal segmental glomerulosclerosis, proteinuria, renal failure, renal disease progression, renal fibrosis
The progression of renal disease depends, among other factors, on the interaction between kidney cells and cytokines (1). Cytokines act on renal cells (tubular cells, mesangial cells and fibroblasts) by inducing proliferation and modifying their phenotypes. These cells start to express a-smooth muscle actin (a-SM-actin) and increase the production of collagen and other extracellular matrix components (1-3). Therefore, the increase of proliferating cell nuclear antigen (PCNA) and a-SM-actin expression by renal cells may be related to renal disease progression. However, although some studies have suggested that markers of renal cell activation and proliferation such as immunostaining of renal biopsies for a-SM-actin and PCNA might be useful diagnostic and/or prognostic indicators in glomerular diseases (3-5), other studies have shown that these immunohistochemical changes observed during renal disease may be reversible (6-8).
The a-SM-actin isoform is normally expressed by vascular smooth muscle cells but interstitial fibroblasts and mesangial and tubular cells can also express this protein in a variety of glomerular diseases. There is some experimental evidence suggesting that transforming growth factor-ß (TGF-ß) and platelet-derived growth factor (PDGF) can induce phenotypic modifications of these cells (9,10). The a-SM-actin synthesis upregulated by these cells is frequently associated with increased cell proliferation and increased extracellular matrix production (1,5, 8,11). PCNA is an acidic nuclear protein whose levels are increased from the late G1 to the S phase of the cell cycle and whose detection parallels other standard methods of assessing cell proliferation such as BrdU labeling and Ki-67 staining (12,13). The aim of the present study was to investigate the expression of a-SM-actin and PCNA in renal cortex from patients with focal segmental glomerulosclerosis (FSGS) and from control individuals and their correlations with parameters of renal disease progression.
We analyzed renal biopsies from patients with idiopathic FSGS (N = 41, 19 males and 22 females) and from 14 control individuals obtained between 1987 and 1998 at the University Hospital of Ribeirão Preto. The study was started in February 1998 and patient follow-up ranged from 2 to 120 months (mean ± SEM, 43.6 ± 6 months). Each patient was submitted to only one biopsy. The diagnosis of idiopathic FSGS was based on the exclusion by clinical and laboratory evaluation of possible causes of secondary FSGS such as syphilis, hepatitis B and C virus infection, HIV, neoplastic diseases, systemic lupus erythematosus, and other collagen diseases. The preserved renal areas of patients submitted to nephrectomy were used as control. The age range of the patients was 3-74 years and the age range of the controls was 2-79 years. Patient plasma creatinine levels ranged from 0.4 to 3.4 mg/dl and proteinuria from 1.0 to 20.8 g/24 h. Plasma creatinine and proteinuria were determined at least every three months during the evolution of the disease. Twenty-two patients presented high arterial pressure (systolic pressure >140 mmHg and diastolic pressure >90 mmHg). After the biopsy, 27 patients were treated with a daily high dose of prednisone (1 mg kg-1 day-1) for 8 weeks. Seven of them presented partial remission (proteinuria <3 g/24 h) and three complete remission (proteinuria <0.3 g/24 h). Cyclophosphamide therapy was introduced for patients with steroid-unresponsive FSGS (proteinuria >3.5 g/24 h) or with relapse (proteinuria >3 g/24 h). However, 17 of these patients failed to respond to treatment. All control subjects had normal plasma creatinine levels (mean ± SEM, 0.80 ± 0.17 mg/dl) and normal arterial pressure and none had urinary abnormalities (proteinuria was not detected by routine methods). The research was approved by the Ethics Committee of the University Hospital of Ribeirão Preto and written informed consent was obtained from all the participants in the study.
Morphological and immunofluorescence evaluation
The tissue obtained by renal biopsy from 41 patients with idiopathic FSGS was fixed in Bouin's solution, embedded in paraffin, cut into 4-µm sections and stained with hematoxylin and eosin, Masson trichrome and methenamine silver. Immunofluorescence analysis of all biopsies was also performed using anti-IgG, anti-IgA, anti-IgM, anti-C3, anti-C1q, anti-kappa, anti-lambda and anti-fibrinogen antibodies in order to confirm the diagnosis. The percentage of glomeruli exhibiting focal or global glomerular sclerosis was determined for each biopsy. The number of glomeruli per biopsy ranged from 5 to 30 (12 ± 7 glomeruli/biopsy). Tubulointerstitial fibrosis was scored as 1 = absent, 2 = mild and focal, 3 = moderate and focal, 4 = severe and focal or mild and diffuse, and 5 = severe and diffuse.
The immunohistochemical studies were performed using a murine monoclonal antibody to an NH2-terminal synthetic form of a-SM-actin (Dako, Glostrup, Denmark) or a monoclonal anti-PCNA antibody (Sigma Chemical Co., St. Louis, MO, USA). Four-micrometer sections of biopsy tissue fixed in Bouin's solution were processed by an indirect immunoperoxidase technique as described (14).
Sections were incubated overnight at 4oC with 1:1000 a-SM-actin antibody or for 30 min at room temperature with anti-PCNA antibody. The reaction product was detected with an avidin-biotin-peroxidase complex (Vector Labs., Burlingame, CA, USA). The color reaction was developed with 3,3-diaminobenzidine (Sigma), and the material was counterstained with methyl green (Sigma), dehydrated and mounted. Negative controls consisted of the omission of the primary antibody in the reaction and of substitution of primary antibody with equivalent concentrations of normal murine IgG. Glomerular expression of a-SM-actin was graded semi-quantitatively according to the following scale (15): 0 = none, 1 = trace mesangial staining, 2 = weak, segmental mesangial staining, usually involving a small minority of glomeruli present, 3 = strong, segmental mesangial staining, usually involving a majority of glomeruli present, and 4 = strong, diffuse mesangial staining, usually involving all glomeruli present. The a-SM-actin immunoreaction in the tubulointerstitium of the renal cortex was scored as follows: 0 = absent staining, 1 = weak staining with focal distribution, 2 = moderate with focal distribution, 3 = strong with focal distribution or weak and diffuse, and 4 = strong and diffuse. A score was assigned to each biopsy, mainly reflecting the changes in the extent rather than intensity of staining. The PCNA reaction was quantified by counting the labeled cells of the glomerular tufts or grid field from the renal cortex, measuring 0.1885 mm2 each, and the mean score per biopsy was calculated by dividing the number of PCNA-positive cells of glomeruli or cortex, respectively, by the number of glomeruli or fields present in each biopsy. The number of fields analyzed per biopsy ranged from 6 to 62 (mean, 18.3).
Determination of plasma creatinine
Plasma creatinine was measured by the Jaffé method (16) and the plasma creatinine level at the time of biopsy was used to determine any correlation between staining for a-SM-actin or PCNA in renal cortex and 1/plasma creatinine (1/Pcreat).
The Spearman correlation coefficient for nonparametric data was used to determine any significant correlation between staining for a-SM-actin or PCNA in the renal cortex and glomeruli and some parameters of renal function and structure of patients with FSGS. The data concerning a-SM-actin score and PCNA obtained from control individuals and from patients with FSGS were submitted to the Mann-Whitney test. The level of significance considered was P<0.050. Plasma creatinine and albumin data are expressed as mean ± SEM and the data concerning scores for tubulointerstitial fibrosis, percentage of glomeruli with sclerosis, a-SM-actin scores, and PCNA in the renal cortex and glomeruli are expressed as median and percentile (25th; 75th).
We observed that the percentage of glomeruli with sclerosis was 44.5 (25.0; 68.3) and the score for tubulointerstitial fibrosis was 2.0 (1.0; 3.0). The plasma creatinine of these patients was 1.62 ± 0.18 mg/dl (mean ± SEM) at the time of biopsy and 3.26 ± 0.61 mg/dl at the last determination. We found a negative correlation between 1/Pcreat at the time of biopsy and the score for tubulointerstitial fibrosis (r = -0.463, P = 0.002). Eighteen of the patients presented a decline of renal function within 43.6 ± 6.00 months, with a plasma creatinine level >2.00 mg/dl at the last evaluation. Proteinuria was 7.36 ± 0.65 g/24 h (mean ± SEM) at the time of biopsy and 4.72 ± 1.42 mg/24 h at the last determination, and we did not observe any correlation between proteinuria and 1/Pcreat at the time of biopsy or the score for tubulointerstitial fibrosis.
Our data also showed an increase of a-SM-actin expression in glomeruli and in the tubulointerstitial area from the renal cortex and of PCNA expression in the tubulointerstitial area from the renal cortex of FSGS patients (Table 1, Figures 1, 2, 3 and 4) (P<0.001). a-SM-actin expression in the glomeruli from these patients was correlated with PCNA expression (r = 0.47, P = 0.003). We also observed that the immunoreaction for a-SM-actin in the tubulointerstitial area was correlated with the intensity of proteinuria at the time of biopsy in FSGS patients (r = 0.363, P = 0.021) (Figure 5). However, we did not find any correlation between the kidney expression of these proteins and 1/Pcreat at the time of biopsy or between the expression of a-SM-actin or PCNA in the glomeruli and tubulointerstitial area and the percentage of glomerulosclerosis or the score for tubulointerstitial fibrosis in the kidneys of these patients. We also did not observe any correlation between the kidney expression of a-SM-actin or PCNA in the glomeruli and tubulointerstitial area and blood pressure at the time of biopsy or the response to treatment.
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Our data showed an increase of a-SM-actin expression in glomeruli and tubulointerstitial area from the renal cortex and of PCNA in the tubulointerstitial area from the renal cortex of idiopathic FSGS patients. Increased expression of these proteins during the evolution of glomerular disease was observed by several investigators (2-8). These alterations were probably induced by some cytokines like TGF-ß and PDGF and by endothelin and angiotensin II and were related to renal injury (1,9,10). Increased renal content and production of these polypeptides have been observed in several glomerular diseases (1,14,17-22), probably induced by glomerular hypertension or hypertrophy, macrophage infiltration, high renal levels of angiotensin and proteinuria observed in these patients (1,14,23-26).
We also observed that the immunoreaction for a-SM-actin in the tubulointerstitial area was correlated with the intensity of proteinuria at the time of biopsy in idiopathic FSGS patients. This fact suggests that the renal handling of protein induced activation of the interstitial cells. It has been suggested that proteins filtered by the glomeruli could be toxic for tubule cells (27-29). Studies with tubule cell cultures have shown that some proteins such as IgG and albumin induce an increase in the production of inflammatory and vasoactive factors (27,28). This observation can explain why greater proteinuria is frequently associated with more severe tubulointerstitial damage.
We did not find any correlation between the kidney expression of a-SM-actin or PCNA and 1/Pcreat at the time of biopsy. This finding might be explained, in part, by the possibility that these alterations detected by immunohistochemical techniques are reversible. Although some studies have suggested that markers of renal cell activation and proliferation such as a-SM-actin and PCNA might be useful diagnostic and prognostic indicators in glomerular diseases, there are some studies showing that these alterations detected by immunochemical techniques in renal diseases can be reduced during the evolution to fibrosis or to recovery (6-8). Hattori et al. (8) performed repeat renal biopsies in patients with FSGS with cellular lesions and observed reduced glomerular a-SM-actin expression associated with progression to glomerular scar formation. Groma et al. (7) demonstrated increased a-SM-actin expression in types of glomerulonephritis with different prognosis. Boukhalfa et al. (6), after studying several glomerulopathies, concluded that a-SM-actin expression in the interstitial area was correlated with interstitial fibrosis but a-SM-actin expression in the glomeruli was reduced with the progression of glomerulosclerosis. We also did not observe any correlation between the kidney expression of a-SM-actin or PCNA in the glomeruli and tubulointerstitial area and the percentage of glomerulosclerosis or the score for tubulointerstitial fibrosis in the kidneys of these patients. Taken together, these findings suggest that the cellular activation verified during the course of renal disease, although important for renal damage, can be reduced during the evolution of renal disease to fibrosis or to recovery. On the other hand, we also have to consider that 18 of these patients presented loss of renal function within a relatively short time (43.60 ± 6.00 months).
a-SM-actin expression in the glomeruli was correlated with PCNA expression, as also reported by Johnson et al. (11). These investigators found that a-SM-actin expression by mesangial cells was associated with active proliferation of these cells.
The present data show an increase of a-SM-actin expression in glomeruli and tubulointerstitial area from the renal cortex and of PCNA in the tubulointerstitial area from the renal cortex of idiopathic FSGS patients. We also observed that the immunoreaction for a-SM-actin in the tubulointerstitial area was correlated with the intensity of proteinuria in FSGS patients. However, we did not find any correlation between the kidney expression of these proteins and 1/Pcreat level at the time of biopsy or renal fibrosis.
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We wish to express our appreciation to Cleonice G.A. da Silva and Erika Delloiagno for expert technical assistance.
Address for correspondence: T.M. Coimbra, Departamento de Fisiologia, FMRP, USP, Av. Bandeirantes, 3900, 14049-900 Ribeirão Preto, SP, Brasil. Fax: +55-16-633-0017. E-mail: firstname.lastname@example.org
T.M. Coimbra and R.S. Costa were recipients of CNPq fellowships. Publication supported by FAPESP. Received August 11, 2000. Accepted May 17, 2001.