Live and Heat-Killed<i> Lactobacillus rhamnosus</i> ATCC 7469 May Induce Modulatory Cytokines Profiles on Macrophages RAW 264.7

Jorjão, Adeline Lacerda; Oliveira, Felipe Eduardo de; Leão, Mariella Vieira Pereira; Carvalho, Cláudio Antonio Talge; Jorge, Antonio Olavo Cardoso; Oliveira, Luciane Dias de

doi:https://doi.org/10.1155/2015/716749

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Research Article | Open Access

Volume 2015 | Article ID 716749 | https://doi.org/10.1155/2015/716749

Live and Heat-Killed Lactobacillus rhamnosus ATCC 7469 May Induce Modulatory Cytokines Profiles on Macrophages RAW 264.7

Adeline Lacerda Jorjão,¹Felipe Eduardo de Oliveira,¹Mariella Vieira Pereira Leão,²Cláudio Antonio Talge Carvalho,³Antonio Olavo Cardoso Jorge,¹and Luciane Dias de Oliveira¹

Academic Editor: Guillermo Tellez

Received03 Aug 2015

Revised20 Oct 2015

Accepted26 Oct 2015

Published16 Nov 2015

Abstract

This study aimed to evaluate the capacity of Lactobacillus rhamnosus and/or its products to induce the synthesis of cytokines (TNF-α, IL-1β, IL-4, IL-6, IL-10, and IL-12) by mouse macrophages (RAW 264.7). Three microorganism preparations were used: live L. rhamnosus (LLR) suspension, heat-killed L. rhamnosus (HKLR) suspension, and the supernatant of a heat-killed L. rhamnosus (SHKLR) suspension, which were cultured with macrophages (37°C, 5% CO₂) for 2 h and 30 min. After that, cells were cultured for 16 h. The supernatants were used for the quantitation of cytokines, by ELISA. The results were compared with the synthesis induced by lipopolysaccharide (LPS) and analysed, using ANOVA and Tukey test, 5%. LLR and HKLR groups were able to significantly increase the production of TNF-α, IL-6, and IL-10 (). SHKLR also significantly increased the production of TNF-α and IL-10 () but not IL-6 (). All the L. rhamnosus suspensions were not able to produce detectable levels of IL-1β or significant levels of IL-4 and IL-12 (). In conclusion, live and heat-killed L. rhamnosus suspensions were able to induce the synthesis of different cytokines with proinflammatory (TNF-α and IL-6) or regulatory (IL-10) functions, suggesting the role of strain L. rhamnosus ATCC 7469 in the modulation or in the stimulation of immune responses.

1. Introduction

According to WHO [1], probiotics are “live organisms which when administered in adequate amounts confer health benefits to the host.” Probiotics such as lactic acid bacteria are known to have antimutagenic [2], anticarcinogenic [3], and antidiarrheal [4] properties besides stimulating the immune system [5, 6] and improving infectious disease resistance [7] and inflammatory gastrointestinal [8]. They help in maintenance of balanced microbiota, improving lactose metabolism [9], and reducing blood pressure and cholesterol [10, 11]. Nevertheless, scientific evidence indicating that inactivated microbes positively affect human health can also be found in the literature [12]. Accordingly, products intentionally containing nonviable microbial cells are already present in the market (e.g., Lactéol Fort from PUMC Pharmaceutical Co., Ltd., and Fermenti Lattici Tindalizzati from Frau, AF United S.p.a.) [13].

The recent widespread use of lactic acid bacteria and bifidobacteria as probiotics can be attributed to scientific evidence that describes their beneficial effects on human health through the modulation of immune system activity [14], although the mechanisms involved in this immune modulation are not yet fully understood. Some of these mechanisms could include altering the balance of cytokines and interacting with cells of the immune system such as phagocytic mononuclear cells (monocytes and macrophages), polymorphonuclear leukocytes (neutrophils), and NK cells, as well as B and T lymphocytes [15].

Maassen et al. [16] showed that the synthesis of cytokines by the intestinal mucosa depends on the strain of Lactobacillus present. They emphasised the need to perform a careful selection of probiotic strain candidates. The benefits, effects, and mechanisms of action of probiotics in a host are yet to be fully elucidated.

Some known probiotic species, such as Lactobacillus rhamnosus, L. acidophilus, and L. plantarum, are used in researches that aim to clarify their benefits to the host [17–21]. Among these species, Lactobacillus rhamnosus is one of the most commonly used therapeutic probiotics. In some recent findings, L. rhamnosus GG showed significant reduction of the incidence of respiratory infections and the duration of diarrhea and improved the symptoms of atopic dermatitis [22]. Besides, L. rhamnosus GG inhibited the toxic effects of Staphylococcus aureus on epidermal keratinocytes [23]. L. rhamnosus M21 activated humoral as well as cellular immune responses, conferring increased resistance to the host against a viral infection [24] and strain of L. rhamnosus ATCC 7469 ameliorated the enterotoxigenic Escherichia coli-induced diarrhea in piglets [25]. L. rhamnosus L34 may produce factors capable of modulating inflammation stimulated by Clostridium difficile [26].

However, many of these beneficial effects are difficult to explain without first understanding the mechanisms responsible for the interaction between Lactobacillus, their secreted products, and host cells. Taking it into consideration, this research aimed to verify the capacity of the probiotic bacteria L. rhamnosus and their products to induce the synthesis of different cytokines by macrophages in vitro.

2. Materials and Methods

2.1. Preparation of Lactobacillus Suspensions

A standard strain of L. rhamnosus (ATCC 7469) was grown in Man-Rogosa-Sharpe (MRS, Oxoid, Basingstoke, Hampshire, England) agar and incubated at 37°C with 5% CO₂ for 24 h, followed by incubation in MRS broth under the same conditions for 24 h. Three different suspensions of L. rhamnosus were then prepared:(1)Live L. rhamnosus (LLR) suspension: the culture was centrifuged for 10 min at 5000 rpm, the supernatants were discharged, and the pellet was suspended in sterile saline. This procedure was repeated two more times. During the last centrifugation, the pellet was suspended in apyrogenic sterile saline at a concentration of 5 × 10⁷ UFC/mL [27].(2)Heat-killed L. rhamnosus (HKLR) suspension: the live L. rhamnosus (LLR) suspension was autoclaved at 121°C for 15 min and centrifuged for 10 min at 5000 rpm, and the supernatant was removed and stored. The pellet was suspended in apyrogenic sterile saline.(3)Supernatant of heat-killed L. rhamnosus (SHKLR) suspension: supernatant was removed and stored of heat-killed L. rhamnosus (HKLR).

2.2. Cell Culture

The RAW 264.7 cell line (APABCAM, Rio de Janeiro, Brazil) was cultured in Dulbecco’s modified Eagle’s complete medium (DMEM, LGC Biotechnology, Cotia, Brazil), supplemented with 10% fetal bovine serum (FBS, Invitrogen, NY, USA) and 20 μg/mL gentamicin, and incubated for 7 days, with medium culture exchange every 2 days, in a humidified atmosphere at 37°C with 5% CO₂. The cells were grown to confluence in 75 cc tissue culture flasks prior to harvesting by scraping using a rubber spatula [27]. Viable cell counts were performed using the method of exclusion with trypan blue (0.5%, Sigma-Aldrich, St. Louis, MO, USA), 10⁶ cells were distributed onto 24-well microplates, and the medium volume was adjusted to 1 mL. The plates were incubated for 18 h (37°C/5% CO₂) to permit cellular adherence prior to experimentation [27]. The supernatant was removed, and the adhered cells were washed twice with apyrogenic sterile saline (NaCl 0.85%). Afterward, 500 μL of fresh DMEM supplemented with 10% fetal bovine serum was added without antibiotics for the culture with live bacteria and with antibiotics (20 μg/mL gentamicin) for the other cultures [27].

2.3. Exposure of Cultures with L. rhamnosus Suspensions

Was added to the wells of the microplates with macrophages 500 μL of each L. rhamnosus suspension, bringing the volume of each well to a total of 1 mL. The cells were incubated for 2.5 h at 37°C with 5% CO₂ [27]. The supernatant was then removed, and the cells were washed twice with apyrogenic sterile saline (NaCl 0.85%). Following this, 1 mL of fresh DMEM supplemented with 10% fetal bovine serum with antibiotic was added, and the cells were incubated for 16 h at 37°C (5% CO₂) [25]. The supernatants were then frozen and stored (at −80°C for approximately 3-4 weeks) prior to subsequent cytokine (TNF-α, IL-1β, IL-4, IL-6, IL-10, and IL-12), as described below.

The tests were performed in triplicate, 4 repetitions per group, for a total of 12 samples of each group (groups: LLR; HKLR; SHKLR; LPS; and negative control). The levels of cytokines generated by exposure of RAW 264.7 cells to L. rhamnosus were compared with those observed in RAW 264.7 cells that were cultured for the same duration with apyrogenic sterile saline (negative control) or LPS of Escherichia coli (10 EU/mL, positive control).

2.4. Quantification of Cytokine Levels

Cytokine levels (TNF-α, IL-1β, IL-4, IL-6, IL-10, and IL-12) were quantified using an enzyme-linked immunosorbent assay (ELISA). The DuoSet ELISA detection kit (R&D Systems, Minneapolis, MN, USA) was used according to the manufacturer’s instructions. In all cases, detection antibody binding was visualized using the streptavidin-horseradish peroxidase conjugate and TMB (trimethylbenzidine) substrate system at an OD of 450 nm. After determining optical densities, cytokine levels (TNF-α, IL-1β, IL-4, IL-6, IL-10, and IL-12, pg/mL) in the macrophage culture supernatants were calculated using the GraphPad Prism 5.0 program. Results were analysed statistically using ANOVA and significant differences among means were determined by using Tukey’s multiple-range test at .

3. Results

The suspensions containing live L. rhamnosus (LLR) or heat-killed L. rhamnosus (HKLR) were able to induce significant production of TNF-α in the same amounts as LPS (). The suspensions with only the products of the microorganism (SHKLR) also significantly induced the production of this cytokine when compared with the negative control, although at a lower level than the other groups (LLR, HKLR, and LPS) () (Figure 1(a)).

(a)

(b)

(c)

(d)

(e)

(f)

Stimulation with LPS (positive control) induces higher IL-6 production compared to the other groups (). The suspensions containing live L. rhamnosus (LLR) or heat-killed L. rhamnosus (HKLR) induced statistically similar IL-6 and this induced significantly higher production to SHKLR groups and negative control group () (Figure 1(b)).

The secretion of IL-1β was not detected after the addition of any of the L. rhamnosus suspensions. Only stimulation with LPS produced detectable levels (Figure 1(c)).

Regarding IL-12, production was almost statistically similar in all groups evaluated (LLR, SHKLR, LPS, and negative control) (). The group stimulated with heat-killed Lactobacillus rhamnosus (HKLR) was the one who differed, with IL-12 levels being statistically lower than the other groups () (Figure 1(d)).

The stimulation of IL-10 production with LPS induced greater production of the cytokines, and this amount was significantly different from the other groups (). The cultures stimulated with LLR, HKLR, and SHKLR also produced significant levels of IL-10 compared with the negative control group (). The HKLR and SHKLR groups were similar to each other () and different from the LLR group () (Figure 1(e)).

The production of IL-4 was detected in only some of the samples of LPS, LLR, and HKLR; however these values were not statistically significant so that all groups (LPS, LLR, HKLR, SHKLR, and negative control) were similar () (Figure 1(f)).

4. Discussion

There are many bacteria with probiotic properties that can present different mechanisms of action, thus inducing different biological and clinical effects on the host [28]. It is always important to highlight the genus, species, and strain to precisely prescribe a probiotic product. In the present study, the standard strain ATCC 7469 of Lactobacillus rhamnosus was used because this strain has been frequently studied for its potential abilities to prevent and treat diseases such as herpes virus type 1, asthma, rheumatoid arthritis, dermatitis, and diarrhea [25, 29–32]. The Lactobacillus genus has also been observed to have important immunomodulatory effects against different pathogens [9, 33]; however, the exact mechanism of action and the best conditions to promote these benefits are not yet defined.

In the present research, macrophages were challenged with L. rhamnosus, and different results in cytokine production were observed. Living or dead L. rhamnosus, as well as their products alone, were able to induce the synthesis of TNF-α, and the suspensions containing live and dead cells of the microorganism generated the same amount of TNF-α as LPS. Other studies have found similar results in macrophage cultures using different probiotic strains [27, 34–36]. Khani et al. [30] also observed that live L. rhamnosus induced higher levels of TNF-α, suggesting that the entire bacteria promoted phagocytosis and consequently increased macrophage activation.

Live or dead L. rhamnosus generated significant levels of IL-6, but these levels were lower than with LPS. Habil et al. [37] observed that L. rhamnosus, Lactobacillus fermentum, Lactobacillus plantarum, Lactobacillus salivarius, and Bifidobacterium breve suppressed the production of IL-6 by macrophages that were primarily stimulated with LPS, showing that probiotics can activate or inhibit cytokine production depending on the conditions. It appears likely that probiotics can moderately stimulate the synthesis of proinflammatory cytokines in the instance of absence of inflammatory response and suppress it in situations of excessive response, which is a remarkable point in this study, once the macrophages had no stimuli with any pathogen.

The supernatant of L. rhamnosus did not induce IL-6 synthesis, thus suggesting the necessity of cell wall components for this event. According to Habil et al. [37], the manner in which the probiotic is introduced to the macrophage can affect cytokine production, that is, whether the products are associated with the wall (contact signal) or released as a soluble product (no contact signals).

In the present study, none of the L. rhamnosus suspensions induced detectable levels of IL-1β. Bleau et al. [38] also reported low levels of IL-1β in macrophages that were stimulated with different extracts of Lactobacillus in cultures and that LPS and live and heat-killed probiotics showed almost the same cytokine level production. Dong et al. [34, 39] observed an increase of this cytokine, however their study focused on mononuclear peripheral blood cells, and they stimulated these cells with different proportions of different probiotic bacteria for longer periods.

Detectable and apparently high levels of IL-12 were observed in all groups, including the negative control group that had the highest mean value, similar to groups stimulated with LPS and live Lactobacillus and supernatant of Lactobacillus. The group stimulated with dead Lactobacillus was the only one to show IL-12 lower levels. Other studies also reported high levels of IL-12 produced by macrophages or mononuclear blood cells that were challenged with probiotic strains [27, 34, 36]. However it appears that IL-12 production can be inhibited by other Gram-positive bacteria, as well as cell compounds such as peptidoglycan. A suspension with dead L. rhamnosus induced lower IL-12 production likely because of higher concentrations of cell wall compounds due to bacteria lysis from autoclaving. Therefore, probiotic bacteria can modulate macrophage function and suppress or increase IL-12 release [37, 40–42] and some cellular components can revert the cytokine profile induced by Lactobacillus, changing, for example, a profile of predominant IL-12 production to a profile of predominant IL-10 production, considered a suppressive cytokine IL-12.

Only a few samples in the study produced detectable levels of IL-4, making it difficult to discuss the effects of probiotics on the secretion of this cytokine. The literature has also reported controversial effects. Amital et al. [43] reported that lots of Lactobacillus strains show inhibitory effect on the release of IL-4 but, on the other hand, they are potent stimulators of IFN-γ, IL-12, and TNF-α, corroborating our results. However, Drago et al. [44] observed that the strains of L. salivarius (LDR0723 and CRL1528) promoted a significant increase in IL-12 and IFN-γ and a reduction of IL-4 and IL-5, while the strains BNL1059 and RGS1746 increased the Th2 response. Drago and coworkers concluded that the modulation response by L. salivarius was strain dependent, meaning that different strains of the same species can produce different cytokines.

The current study shows that L. rhamnosus, as well as their products alone, were able to induce the synthesis of proinflammatory cytokines and possibly a response profile of Th1 type, which is important in the defense against intracellular pathogens most and contrary to hypersensitivity frames, which are usually caused by imbalance in Th2 anti-inflammatory response. Lactobacillus were also able to induce IL-10 production, which has the regulatory functions and can inhibit Th1 response and when excessive can lead to tissue damage. Therefore there must be a balance between these responses (Th1/Th2), and these bacteria, L. rhamnosus, seem to have potential role in the modulation as well as the maintenance of the immune system balance. Rajput et al. [45] also showed that the administration of the probiotic strains of Saccharomyces boulardii and Bacillus subtilis B10 was able to increase the production of IL-10 in chickens.

However, it is important to note that this is an in vitro study. We used only one lineage of resting cells, because they had not been subjected to any treatment or early stimulation. Our experimental conditions were different from in vivo conditions, where many cells are present. Most importantly, our experiment did not take into consideration the effects of lymphocytes, which are the primary cells in cytokine production and in the organization of adaptive responses. In vivo situations present a more complex system in which other stimuli such as pathogens act and interact.

Live and heat-killed L. rhamnosus suspensions were able to induce the synthesis of different cytokines with proinflammatory (TNF-α and IL-6) or regulatory (IL-10) functions, suggesting that L. rhamnosus ATCC 7469 is capable of exerting immunoregulatory effect on macrophages.

Conflict of Interests

The authors declare that they have no conflict of interests.

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Copyright © 2015 Adeline Lacerda Jorjão et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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