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On-line version ISSN 1414-431X
Braz J Med Biol Res vol.35 no.1 Ribeirão Preto Jan. 2002
Braz J Med Biol Res, January 2002, Volume 35(1) 17-24
Characterization of renin mRNA expression and enzyme activity in rat and mouse mesangial cells
Disciplina de Nefrologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brasil
Material and Methods
Correspondence and Footnotes
Renin is an enzyme involved in the stepwise generation of angiotensin II. Juxtaglomerular cells are the main source of plasma renin, but renin activity has been detected in other cell types. In the present study we evaluated the presence of renin mRNA in adult male Wistar rat and mouse (C-57 Black/6) mesangial cells (MC) and their ability to process, store and release both the active and inactive forms of the enzyme. Active renin and total renin content obtained after trypsin treatment were estimated by angiotensinogen consumption analyzed by SDS-PAGE electrophoresis and quantified by angiotensin I generation by HPLC. Renin mRNA, detected by RT-PCR, was present in both rat and mouse MC under basal conditions. Active renin was significantly higher (P<0.05) in the cell lysate (43.5 ± 5.7 ng h-1 106 cells) than in the culture medium (12.5 ± 2.5 ng h-1 106 cells). Inactive prorenin content was similar for the intra- and extracellular compartments (9.7 ± 3.1 and 3.9 ± 0.9 ng h-1 106 cells). Free active renin was the predominant form found in both cell compartments. These results indicate that MC in culture are able to synthesize and translate renin mRNA probably as inactive prorenin which is mostly processed to active renin inside the cell. MC secrete both forms of the enzyme but at a lower level compared with intracellular content, suggesting that the main role of renin synthesized by MC may be the intracellular generation of angiotensin II.
Key words: Renin, Prorenin, Mesangial cell, Kidney
Systemic angiotensin II plays a pivotal role in the regulation of blood pressure and in fluid and electrolyte homeostasis. The renin-angiotensin system (RAS) consists of four main proteins: renin, angiotensinogen, angiotensin I-converting enzyme (ACE) and angiotensin II receptor. Renin is a rate-limiting enzyme in the synthesis of angiotensin II (1) and juxtaglomerular cells in the kidney are the main source of plasma renin, responsible for cleavage of angiotensinogen into angiotensin I, initiating the cascade for systemic angiotensin II formation. About 80% of intracellular renin has little or no enzymatic activity and is called inactive renin or prorenin (2). Inactive renin can be converted into the active form through limited proteolysis at physiological pH by tissue proteases such as trypsin and kallikreins (3,4), but probably by cathepsin B in vivo (5).
In addition to systemic angiotensin II generation, increasing evidence has suggested that several organs and tissues are able to locally synthesize angiotensin II (6). In the kidney, proximal and distal tubular epithelial cells express genes encoding for all RAS components (7). In addition, it has been recently demonstrated that human mesangial cells express mRNA for renin, angiotensinogen and ACE (8,9). Moreover, renin activity has been also demonstrated in these cells (10) although it is not known if mesangial cells, like juxtaglomerular cells, are able to store, process and secrete the active form of the enzyme, which may constitute a local endocrine system serving paracrine and autocrine functions. Thus, the objectives of the present study were to determine if mouse and rat mesangial cells in culture are able to express and translate renin mRNA and secrete the active form of renin.
Primary culture of rat and mouse mesangial cells
Glomerular mesangial cells were cultured from kidneys freshly removed from normal adult male Wistar rats and mice (C-57 Black/6) as previously described (11). Briefly, kidney cortex was macrodissected, fragmented, forced through a graded series of stainless-steel sieves (60, 100, and 200 meshes), and rinsed with RPMI 1640 culture medium. The glomeruli were then collected from the surface of the third sieve and forced through a 25 x 7 gauge needle for full decapsulation. Glomeruli were plated at a density of ~300 glomeruli/cm onto RPMI 1640 supplemented with 20% FCS, 50 U/ml penicillin, 2.6 g acid HEPES and 2 mM glutamine. All reagents were from Sigma (St. Louis, MO, USA). Culture flasks were kept in a 95% air and 5% CO2 humidified environment at 37ºC. The medium was replaced every 36 h. After 3 weeks cells were harvested with trypsin and the subcultures were grown in the same culture medium. Cells were used between the 3rd and 5th subculture. Mesangial cells were characterized by previously established criteria, including morphological appearance of stellate shape, positive immunofluorescence staining for actin and myosin and negative staining for human factor VIII (11).
Total RNA extraction
Total RNA was isolated from rat and mouse kidney cortex and from mesangial cells by the guanidine isothiocyanate-cesium chloride method. The RNA pellet was dissolved in RNase-free water and RNA concentration was estimated with a spectrophotometer (Gene Quant RNA/DNA calculator, Amersham Pharmacia Biotech, Uppsala, Sweden).
RT-PCR. Two micrograms of total RNA was reverse transcribed by the addition of a mix containing 0.5 mg/ml oligo d(T) primer (Pharmacia Biotech), 10 mM DTT, 0.5 mM mixed dNTPs (Pharmacia Biotech), and 200 U reverse transcriptase (SuperScript RT, Gibco-BRL, São Paulo, SP, Brazil). The mixture was incubated at 37ºC for 1 h. PCR was performed in a thermal cycler (model PTC-100, MJ Research, Watertown, MA, USA) using 2 µl of cDNA in a total volume of 20 µl containing 1.0-2.5 mM MgCl (optimized for each pair primer), 0.5 mM of each primer, 0.5 mM dNTP mix and 0.5 U Taq DNA polymerase (Pharmacia Biotech). Primer sequences and amplification conditions for each primer pair are shown in Table 1.
Negative controls were included in each set of PCR assays where cDNA was substituted for water as a control for contamination from exogenous sources. In addition, reverse transcriptase was omitted in some samples as a negative control for amplification of genomic DNA. Positive controls included amplification of kidney cortex cDNA and the efficiency of the reverse transcriptase reaction was monitored by ß actin cDNA amplification. PCR products were electrophoresed on 1% agarose gel and visualized by ethidium bromide staining under UV light.
Intracellular renin activity
Total intracellular renin activity was determined in both rat and mouse mesangial cells on the basis of angiotensinogen consumption. Cells were rinsed twice with PBS and lysed with 1 mM Tris-HCl buffer. Cell homogenates were treated with enzymatic inhibitors (50 mM EDTA, 312 mM PMFS, 1.0 mM Ophe and 200 mM DTT) specific for enzymes able to cleave renin and angiotensinogen, including serine-, thiol- and metalloproteinases. In addition, a homogenate aliquot was treated with trypsin (50 µg/ml) for 16-18 h at 37ºC in order to activate inactive prerenin. Samples were then incubated with sheep angiotensinogen (1 mg/ml) for different periods of time (0, 4, 8, 12 and 24 h) at 37ºC and the reaction was interrupted by the addition of 50% H3PO4. Angiotensinogen consumption was analyzed by SDS-PAGE on 7.5% polyacrylamide slab gel by the method of Laemmli (12), stained with a Silver Stain kit (BioRad Laboratories, Hercules, CA, USA) and semi-quantified by densitometric analyses (Quik scan).
Renin content analysis
The content of active and inactive forms of renin was determined and quantified in rat primary mesangial cells in the intracellular compartment and in the culture medium, characterizing the secreted forms. The culture medium was collected and stored at -70ºC until the time for use. Cells were rinsed with PBS, lysed with 1 mM Tris-HCl buffer and stored until the time for use. Total content of renin included active renin (free form) and the inactive prorenin form, activated with 10 µl of trypsin (50 µg/ml) for 16-18 h at 37ºC. The free renin (active) content was evaluated in the absence of trypsin. In addition, cell homogenate and culture medium were incubated with enzymatic inhibitors as described above to protect the angiotensin I released. The content of renin was estimated by angiotensin I generation when cell lysate or culture medium was incubated with 10 µl of a synthetic tetradecapeptide substrate, 1 mg/ml (kindly supplied by Dr. Luis Juliano, Biophysics Department, UNIFESP, São Paulo, SP, Brazil) for 0, 4, 8, 12 and 24 h at 37ºC. The reaction was interrupted with 10 µl of 50% H3PO4. After interruption of the reaction at different times of incubation, 100 µl of each sample was filtered and injected into the HPLC system. The released angiotensin I peptide was analyzed by reversed phase HPLC using an aquapore ODS 300 column equilibrated with 0.1% phosphoric acid containing 5% acetonitrile (v/v). Angiotensin I was separated by isocratic elution for 5 min followed by a 20-min linear gradient of 5-35% acetonitrile in 0.1% phosphoric acid (v/v) at 1.5 ml/min. The chromatographic profile of each sample was compared with that obtained for standard samples containing angiotensinogen (retention time = 20.23 min) and angiotensin I (retention time = 19.59 min) at absorbance of 240 nm, AUF = 0.02. Peptide fragments were identified by elution position and quantified by integration area using repeated injections of standard peptide solution to correct for small differences in retention time (<6%) and peak height (<5%).
PCR amplification of renin mRNA from rat and mouse mesangial cells
RT-PCR. Figure 1 shows a representative gel of RT-PCR-amplified products for mouse (1A) and rat (1B) renin cDNA. cDNA obtained from whole kidney was used as positive control. The negative control for each cDNA synthesis reaction consisted of the absence of reverse transcriptase. The specific primer pairs for different animal species were able to amplify the expected product size for mouse (291 bp) and rat (362 bp) mesangial cells.
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Intracellular renin activity present in rat and mouse (Figure 2) mesangial cells was estimated by angiotensinogen consumption and visualized on polyacrylamide gel. Densitometric analysis showed a slow but progressive reduction in band intensity in the presence of basal renin activity (panel A). The consumption was accelerated when inactive renin was pre-activated with trypsin (panel B), indicating that mesangial cells store renin in its inactive form, but ready to be activated.
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The generation of angiotensin I was used to estimate active and total intracellular renin activity. Figure 3 shows a representative experiment analyzing HPLC-injected cell homogenate samples preincubated with trypsin and then incubated with angiotensinogen to determine total renin activity. As can be seen, the angiotensinogen peak was reduced and the angiotensin I peak was increased over time (4, 8, 12 and 24 h). After 24 h of incubation, the angiotensinogen peak almost disappeared while the angiotensin I peak was substantially increased, indicating that a substantial quantity of angiotensinogen was hydrolyzed, releasing angiotensin I.
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Quantification of stored and secreted forms of renin
Based on the HPLC profiles of the released angiotensin I, the relative content of active and inactive forms of renin present in the intracellular compartment and in the culture medium was quantified in rat mesangial cells. Results are reported as ng h-1 106 cells (Table 2 and Figure 4). Inactive prorenin content was estimated from the difference between total and active renin. Mean intracellular active renin content was 43.5 ± 5.7 ng h-1 106 cells, corresponding to 83 ± 5% of total renin content, while prorenin content (9.7 ± 3.1 ng h-1 106 cells) corresponded to 17 ± 5%. In the culture medium the predominant form was also active renin (76 ± 6%) compared with inactive prorenin (24 ± 1%). However, the secreted forms of both active and inactive renins were present at lower levels compared with intracellular levels, especially active renin (12.5 ± 2.5 vs 43.5 ± 5.7 ng h-1 106 cells, P<0.05).
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In juxtaglomerular cells, renin is first synthesized as the protein precursor preprorenin. In rough endoplasmic reticulum, the signal sequence is excised from preprorenin to yield prorenin, the inactive form of the enzyme (13-15). It has been demonstrated that the partial proteolytic activation of prorenin occurs within maturing secretory granules responsible for constitutively releasing both the inactive and active forms of renin. Active renin is also released by juxtaglomerular cells from mature secretory granules by a regulated pathway (16,17). In addition to juxtaglomerular cells, renin activity has been demonstrated in other cell types including kidney cells. Since the secretory function of mesangial cells has been implicated in several autocrine and paracrine activities, the present study evaluated the ability of mouse and rat mesangial cells to express renin mRNA as well as to synthesize, store and secrete both the active (renin) and inactive (prorenin) forms of the enzyme.
The RT-PCR amplification products obtained from mouse and rat mesangial cell cDNAs using specific primers indicated that both cell populations are able to constitutively express renin mRNA. Renin activity has been detected in rat and human cultured mesangial cells (10,18). The renin activity in these cells may derive from intracellular synthesis of renin by renin gene activation or from an extracellular source (culture medium) or from a "renin-like" enzyme, as suggested by Shenoy and Cassis (19) for brown adipose tissue. However, the presence of renin mRNA has been demonstrated in human glomerular epithelial and mesangial cells in culture but apparently at very low levels since it was necessary to use the highly sensitive nested PCR technique to detect renin mRNA under normal conditions (8). In contrast, in the present study a simple RT-PCR was sufficient to detect renin mRNA in rat and mouse mesangial cells under basal conditions. Whether the constitutive transcription of the renin gene in rat and mouse mesangial cells is higher than in human mesangial cells in culture cannot be determined from these studies, but the data strongly suggest that the renin activity previously detected in these cells is a consequence of renin gene activation.
In order to determine if renin gene transcription in mesangial cells, like in juxtaglomerular cells, results initially in inactive prorenin and if these cells have the ability to process prorenin to active renin, we evaluated free renin activity content and the total content of renin after preactivation of prorenin with trypsin. Intracellular renin activity was higher in the presence of trypsin, indicating that mesangial cells may store and process the inactive form of the enzyme. However, the predominant form found in the cell lysate under basal conditions was active renin, responsible for ~85% of total intracellular renin activity. This result agrees with previous data obtained for human mesangial cells (10) or other renin-producing cell types including juxtaglomerular cells (20-22).
The presence of renin activity was also evaluated in the culture medium in order to characterize the secreted forms of the enzyme. The levels of both renin and prorenin were much lower than those found in the intracellular compartment. However, the predominant secreted form was active renin, corresponding to 75% of total renin activity. In contrast, many cell types secrete mainly inactive prorenin. Juxtaglomerular cells, the main source of circulating renin, secrete both active and inactive prorenin, but the inactive renin can be present at three to five times the level of active renin in the circulation of humans (15). The reason why these cells secrete large quantities of inactive enzyme is not clear, since prorenin appears not to be activated in the circulation (23,24) or to act as an endogenous antagonist for the effects of renin, at least in the vascular wall (25). The present results suggest that the main role of renin produced by mesangial cells may be the intracellular generation of angiotensin II, since only a minor quantity of active renin appears to be secreted by mesangial cells. Moreover, both ACE and angiotensinogen have been detected in mesangial cells in culture (8,9), and therefore these cells have all the components necessary to locally synthesize angiotensin II independently of systemic and/or other tissues. Although at low levels, both forms of renin were found in culture medium. Whether these secreted forms have physiological and/or pathophysiological implications needs further investigation.
Renin activity present in the cell lysate was intensified after activation of prorenin with trypsin since the consumption of angiotensinogen was faster after activation, suggesting that mesangial cells are able to store renin in the inactive form, but ready to be activated under a stimulus.
These results indicate that mesangial cells are able to constitutively synthesize and process prorenin to active renin in the intracellular compartment and also to secrete both forms of the enzyme.
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Address for correspondence: M.A. Boim, Disciplina de Nefrologia, EPM, UNIFESP, Rua Botucatu, 740, 04023-900 São Paulo, SP, Brasil. Fax: +55-11-5573-9652. E-mail: firstname.lastname@example.org
Research supported by CNPq and Fundação Oswaldo Ramos, UNIFESP. Publication supported by FAPESP. Received April 11, 2001. Accepted October 2, 2001.