key: cord-030385-btf502ju
authors: Sun, Zhiheng; Pan, Yuchen; Qu, Junxing; Xu, Yujun; Dou, Huan; Hou, Yayi
title: 17β-Estradiol Promotes Trained Immunity in Females Against Sepsis via Regulating Nucleus Translocation of RelB
date: 2020-07-22
journal: Front Immunol
DOI: 10.3389/fimmu.2020.01591
sha: 
doc_id: 30385
cord_uid: btf502ju

Sepsis is more common among males than females, and the unequal estrogen levels have been suspected to play a vital role in gender differences. Recently, trained immunity is reported to be a novel strategy for the innate immune system to fight infection. However, it has not been clarified whether β-glucan-induced trained immunity causes different responses to early sepsis between male and female mice. In this study, sepsis was induced in mice by intraperitoneal injection of Escherichia coli (E. coli). The changes of inflammatory cytokines expression, and macrophage polarization in male, female, and ovariectomized C57BL/6 mice in sepsis model were investigated. For in vitro studies, different macrophages were treated with LPS. The function of estradiol (E2) on macrophage cell lines was verified and the mechanism of E2 affecting trained immunity was explored. We demonstrated that β-glucan-induced trained immunity was more resistant to sepsis in female than male mice. Macrophage polarization toward the M1 phenotype, which exhibited enhanced trained immunity, was related to the difference in sepsis resistance between female and male mice. Moreover, ovariectomized (OVX) mice manifested serious sepsis consequences with a weaker trained immunity effect than female mice. Female bone marrow-derived macrophages (BMDMs) were also apt to be polarized to the M1 phenotype in response to trained immunity in vitro. Furthermore, E2 promoted trained immunity in macrophage cell lines J774 and RAW264.7. E2 was also verified to facilitate trained immunity in primary BMDMs from female and male mice. Mechanistically, we found that E2 inhibited the nuclear translocation of RelB, which is a member of non-canonical pathway of NFκB and contributes to macrophage polarization to change the intensity of trained immunity. This study is the first to indicate the role of E2 in the trained immunity induced by β-glucan to protect against E. coli-induced sepsis via the non-canonical NFκB pathway. These results improve our understanding of the molecular mechanisms governing trained immunity in gender differences.

Sepsis is a systemic reaction, which can even be caused by an ordinary infection (1) . The infection is most commonly bacterial but also can be fungal, viral, or parasitic. Since many organs are affected, the mortality rate of sepsis is 30-50% (2) . With the development of modern medicine, the mortality rates have declined to about 30% (3), but this is still far from acceptable. The biomarker of sepsis is widely discussed by a number of reviews (4) (5) (6) (7) . Several important signs of sepsis are damage to the kidney, liver, and lung, as well as an increased bacterial load in the kidney and elevated levels of transaminase and lactate in serum (8) . Moreover, the common model of sepsis is an immune response to Escherichia coli or endotoxin, lipopolysaccharide (LPS), found in the cell wall of gram-negative bacteria. Endotoxin is an excellent example of a pathogen-associated molecular pattern (PAMP). Of note, a number of studies indicate gender dimorphism in terms of response to sepsis (5) . The intuitive result is that the incidence of female sepsis is much lower than that of males (9, 10) . Furthermore, some studies attributed these differences to the prevailing hormonal milieu of the victim (11) (12) (13) . Thus, it is necessary to explore the mechanism of estrogen in modulating immunity, which allows females to resist sepsis.

The NFκB (nuclear factor kappa-B) family of transcription factors constitutes five members (RelA or p65, RelB, cRel, NFκB1 or p50, and NFκB2 or p52), all of which play important roles in cell homeostasis, especially in the immune process (14) . Apart from the well-known canonical signaling pathway, the noncanonical pathway is also involved in vital immune processes, which could be triggered by signaling from a subset of TNFR members. This pathway mediates the persistent activation of RelB/p52 complex with the ability to modulate a series of gene expression, including macrophage polarization-associated cytokines. To date, a growing number of studies indicated that estrogen is involved in some immune processes. Estrogen can bind to and activate estrogen receptors (ERs), which regulate the expression of downstream genes (15) . The interaction between ERs and NFκB is mainly discussed in breast cancer articles (16) . A highly significant negative correlation between the expression of NFκB target genes and ER activation was found. Some studies Abbreviations: E 2 , 17-β-estradiol; TI, trained immunity; LPS, lipopolysaccharide; PBS, phosphate buffer saline; AST, aspartate aminotransferase; ALT, alanine aminotransferase; IL-6, interleukin-6; TNFα, tumor necrosis factor α; IL-10, interleukin-10; IL-4, interleukin-4; M-CSF, macrophage colony-stimulating factor. demonstrated the interaction of ER with NFκB; ERs can compete with NFκB for binding to transcriptional coactivators (ie, CREB) or ERs to recruit co-suppressors into NFκB complexes (17) . ERs can inhibit de novo RelB synthesis in breast cancer tissues and cell lines. In addition, E 2 inhibits the nucleus translocation of P65, c-Rel, and RelB without affecting P50 in mouse splenocytes (18) . These data suggest that estrogen-ER signaling regulates the NFκB pathway at the transcriptional level of its constituents.

The host's immune defense mechanisms can be divided into innate immunity and adaptive immunity. Adaptive immunity, although slower than the innate immune response, has good specificity and produces immunological memory (19) . Recently, researchers discovered an ability in innate immunity, similar to immune memory in adaptive immunity, called trained immunity (20) . Trained immunity is found in mammals and its basic features have been identified by several researchers. Trained immunity mainly involves a set of cells (myeloid cells, natural killer cells, and innate lymphoid cells) (21) . Antituberculosis vaccine Bacillus Calmette-Guérin (BCG) is a wellknown immune modulator that induces trained immunity. It was reported that estrogen did not influence the induction of trained immunity by BCG, and did not induce training or tolerance in monocytes themselves, indicating that the estrogen is unlikely to explain the sex-differential effects after BCG vaccination (22) . In fact, β-glucan is a major cell wall component of C. albicans and can induce trained immunity in monocytes. The initiation of trained immunity is associated with enhanced signaling of the Akt (protein kinase B)-mTOR (mammalian target of rapamycin)-HIF-1α (hypoxia-inducible factor-1α) pathway (23) , modifications in metabolic pathways (conversion to glycolysis), and epigenetic rewriting (24, 25) . However, the effect of estrogen on β-glucan-induced trained immunity to resist sepsis has not been clarified.

β-glucan (G-59303) and β-Estradiol (50-28-2) were purchased from XiEnSi biotechnology company (Tianjin, China). M-CSF (#CB34), IFN-γ (#C746), and TNFα (#CF09) were purchased from Novoprotein (Shanghai, China). E 2 and LPS was purchased from Sigma (St. Louis, MO, USA). Antibody against p-Akt (Ser473, #4060), Akt (#4691), p-4EBP1 (#2855), 4EBP1 (Thr37/46, #9644T), p-S6 (Ser235/236, #4858), S6 (#2217), PCNA (#13110), P65 (#8242), Estrogen receptor α (13258s), GAPDH (#5174), and β-Actin (#3700) were purchased from Cell Signaling (Boston, MO, USA). RelB (sc-166416) was purchased from Santa Cruz Biotechnology (Dallas, TX, USA). F4/80-APC, F4/80-FITC, CD116-PE, CD206-APC, CD206-FITC, iNOS-PE were all from Biolegend (San Diego, CA, USA).

Raw264.7, J774, and HEK293T cells were obtained from the Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China. Cells were cultured in phenol red-free DMEM with 10% FBS, 1% (100 U/mL penicillin and 100 ug/mL streptomycin) at 37 • C in an atmosphere of 95% air and 5% CO 2 . Cells were seeded onto different types of plates for further experiments when the cell density reached ∼80%. The cells were used within a maximum of five passages.

The in vitro trained immunity model was established with RAW264.7 and J774. Cells were challenged with 5 µg/mL βglucan for 24 h. The cells were then washed and rested in culture medium for 5 days. Next, cells were treated with 100 ng/mL LPS for 6 h, and then the cytokines were measured in mRNA level.

1 × 10 5 BMDMs were seeded in 96-well plates (200 µL final volume; Corning) and stimulated with 100 µg/mL β-glucan for 24 h. Then cells were washed and rested for 3 days in culture medium. On day 4, BMDMs were washed again and treated with 25 ng/mL IFN-γ for 24 h. On day 5, a final wash was performed, and cells were primed with 1 µg/mL LPS. The supernatants were harvested for ELISA assay after 24 h of LPS stimulation. Other experiments were all based on the same model but with different numbers of BMDMs. To assess mRNA expression and cell viability, 6 × 10 5 BMDMs were plated in non-treated 24well plates (1,200 mL final volume; Corning) and followed the training scheme described above. For western blotting (WB) assays 3 × 10 6 BMDMs were plated in six-well plates (3 mL final volume; Corning).

Male and female C57BL/B mice were purchased from the Model Animal Research Center of Nanjing University. Mice used in the model of trained immunity and sepsis were 10 weeks old. All animal procedures were performed in accordance with guidelines of the US NIH with Specific Pathogen Free conditions. Soyfree standard rodent chow and water were provided ad libitum. Female mice were anesthetized with 4% chloral hydrate and then underwent ovariectomy (OVX) at 6 weeks of age. When they were 10 weeks old, the same model of trained immunity and sepsis was established.

Peripheral blood mononuclear cells (PBMCs) were separated from mouse plasma by Ficoll centrifugation using lymphocyte separation medium from MP Biomedicals (Solon, USA) according to the standard procedures.

Mice were sacrificed via cervical dislocation and sterilized by soaking in 75% ethanol. Dissected the legs and bone marrow was extracted from tibia and femur bones by using a 25-gauge needle and a 1 mL syringe filled with PBS following removal of surrounding muscle. Blow the bone marrow gently and spread it through a 70 µm cell strainer. The cell suspension was centrifuged at 300 g for 5 min at room temperature. Cells were cultured in phenol red-free DMEM with 10% ultra-low endotoxin FBS and M-CSF (20 ng/mL). After changing the fresh medium on the third and fifth day, BMDM was induced.

The E. coli 15597 strains were purchased from ATCC, collected, and identified by the Medical Laboratory Center of Zhongda Hospital in Nanjing Jiangsu, China, and stored at −80 • C. Bacterial strains were prepared in LB medium.

A nuclear protein extraction kit was purchased from Biyuntian (Wuhan, China) and used according to the manufacturer's instructions.

siRNA Transfection siRNA was transfected according to the product instructions (Ruibo company, China). The concentration of siRNA used in the study was 50 nM. The ERα siRNA target sequence is TGCACATTGAAGATGCTGA. The target sequence of non-coding (NC) siRNA was a random sequence with no biological effects.

To assess the effect of E 2 on cell viability, a CCK-8 assay was used according to the manufacturer's instructions (Bioss company, China). RAW264.7/J774 were seeded onto 96-well plates at a concentration of ∼5 × 10 4 cells/well. Different concentrations of E 2 were used to treat cells for different length of time as described in the article.

Total RNA was extracted from cells using TRIzol reagent, and reverse transcriptions were performed in a 20 µL mixture with 1 µg of total RNA according to the manufacturer's instructions (Vazyme company, China). The oligonucleotide primers used for PCR amplification are listed in Table 1 . PCR amplification consisted of 30 cycles of denaturation at 95 • C for 2 min, annealing at 60 • C for 45 s, and extension at 72 • C for 2 min. All reactions were run in triplicate. The gene expression levels were normalized to ß-actin.

The protein samples were obtained from lysis buffer treated cells. Cell lysates were put on ice for 15 min and then centrifuged at 12,000 × g for 10 min. Subsequently, 30 µg of protein per lane was separated on 10% polyacrylamide gels and transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, USA). Membranes were blocked with 5% bovine serum albumin (BSA) in Tris-buffered saline containing 0.1% Tween 20, and then the membranes were incubated with specific antibodies. The values were normalized to the β-actin/GAPDH intensity levels.

Mice were trained with two intraperitoneal (i.p.) injections of 1 mg β-glucan particles on days −7 and −4. Sterile PBS was used as a control. On day 0, mice were challenged with 1.77 × 10 7 E. coli. The lung, kidney, and serum were harvested 24 h after E. coli treatment.

The fresh lung tissues were fixed in 4% paraformaldehyde (PFA). Then, the samples were gradually dehydrated and embedded in paraffin. After that, the samples were cut into 3 µm sections and stained with hematoxylin and eosin for further light microscopy observation. Scores were evaluated by a pathologist based on the lung tissue integrity, alveolar integrity, and mononuclear infiltration (0 = none; 1 = mild; 2 = moderate; 3 = severe).

Cultured cells were seeded on glass coverslips in six-well plates.

After three PBS washes, the samples were fixed for 15 min at room temperature with 4% paraformaldehyde. Fixed cells were rinsed with PBS and then incubated for 10 min at 4 • C with 0.2% Triton X-100 and 0.2% BSA in PBS. Following permeabilization, non-specific binding in the cells was blocked by 5% BSA in PBS for 1 h at room temperature. Cell samples were incubated with anti-ERα, anti-RelB, and anti-p65 primary antibodies at a 1:200 dilution for 2 h at room temperature. Samples were further incubated with Alexa Fluor 488-conjugated and Alexa 647conjugated secondary antibody at a 1:400 dilution for 1.5 h in the dark. After washed with PBS, the nuclei were stained by DAPI. Slides were visualized using a Nikon Eclipse Ti-U fluorescence microscope equipped with a digital camera (DS-Ri1, Nikon).

The protein concentration of IL-6, lactate, TNFα, and estrogen in cell supernatant or mouse serum were detected using the corresponding mouse enzyme-linked immunosorbent assay (ELISA) kit according to the manufacturer's instructions (Biolegend, China).

The kidney E. coli burden at indicated time points was measured by plating organ homogenates obtained mechanically over 70 µm cell strainers (BD Biosciences) following slicing the tissue, in serial dilutions on LB agar plates; colony-forming units (CFUs) were counted after growth at 37 • C for 24 h, and data are shown as CFUs in total kidney.

PBMCs or BMDMs were filtered through a 70 µm cell strainer and then washed with complete RPMI medium to generate single-cell suspensions. An Fc-receptor blocker (CD16/32, eBioscience) was used to reduce non-specific antibody binding. Antibodies used in these experiments included F4/80-APC, F4/80-FITC, iNOS-PE, CD206-APC, and CD11b-PE. Stained samples were detected by a FACS Calibur flow cytometer (BD Bioscience) and data were analyzed using FlowJo software (TreeStar, Ashland, OR).

The statistical analysis was performed using Prism (Prism 5 for Windows, GraphPad Software Inc., USA). Unless specified, statistical significance for comparison between two sample groups with a normal distribution (Shapiro-Wilk test for normality) was determined using two-tailed paired or unpaired Student's t-test. Differences were considered significant at p < 0.05 as indicated. Except when specified, only significant differences are shown. As indicated in figure legends, either a representative experiment or a pool is shown, and the number of repetitions of each experiment and number of experimental units (either cultures or mice) is indicated. The results are presented as the means ± standard error (SEM).

Several studies have shown that women have better survival and tolerance to sepsis than men (26, 27) . Thus, we further verified this phenomenon by establishing a sepsis model in mice ( Figure 1A) . The difference in lung injury between male and female mice in sepsis was determined by H&E analysis of lung sections (Figure 1Ba) . The histochemical scores (Figure 1Bb ) indicated that male mice had more severe lung damage than female mice; trained immunity prevented lung injury in mice and the protective effect of trained immunity was better for females than males. Notably, we observed a decreased renal E. coli burden in females than males. In addition, in trained immunity mice, females had less renal E. coli burden than males (Figures 1C,D) .

In addition, liver damage markers, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) were increased in males than females; and trained immunity markedly decreased AST and ALT concentration, with a greater decrease in females than in males (Figures 1E,F) . We found that in the sepsis model, the serum lactate concentration of the male mice was higher than that of the female mice. In the trained immunity group, serum lactate was decreased, with the level in the females lower than males ( Figure 1G ). As expected, male serum E 2 content is much lower than female mice ( Figure 1H) . Our results showed that females expressed higher IL-6 and TNFα than males in sepsis, and trained immunity exacerbated this trend (Figures 1I,J) .

Macrophages are the most significant cells in the body in regard to trained immunity (28) . The promoted trained immunity is related to the increased M1 phenotype macrophage. In order to understand the different response to sepsis between the different genders, we further investigated the polarization of macrophages during the process. Thus, we focused on macrophage content and polarization. By detecting the percentage of macrophages in the spleen, we found that macrophages in female mice are more abundant than male mice, and trained immunity significantly increased the content of female macrophages (Figure 2A) . Sepsis promoted the polarization of macrophages to M1 and trained immunity aggravated this trend. Notably, females showed more changes than males (Figure 2B) . On the other hand, females inhibited the polarization of M2 macrophages ( Figure 2C) . Trained immunity simulated M1type polarization of macrophages, and this effect was more pronounced for females.

By analyzing the experiments above, we found that the difference between male and female responses to sepsis was due to the difference in macrophage polarization in vivo, and the difference in estrogen content in the different genders was very significant.

To verify that differences in the estrogen level play a vital role, OVX mice were made, since the ovary is the main organ to produce E 2 . The same sepsis model was established with OVX mice (Figure 1A) . Firstly, the serum E 2 concentration was significantly decreased (Figure 3A) . The degree of lung injury was much higher than that of female mice as well as TI + E. coli group (Figure 3B) . The kidney E. coli burden was also evaluated. The results showed that OVX mice also had more severe kidney injury ( Figure 3C ) as well as lung injury, as measured by serum ALT (Figure 3D ) and AST ( Figure 3E ) concentrations, in comparison to female mice. With a lower serum IL-6 and TNFα concentration in OVX mice in the TI + E. coli group, the data suggested that OVX mice have a lower trained immunity response than female mice (Figures 3F,G) . Finally, similar to male mice, OVX mouse PBMCs began polarizing to M2-type at 24 h after i.p. E. coli ( Figure 3H ). Taken together, these results demonstrated that E 2 does facilitate trained immunity in the body to resist sepsis, and simultaneously inhibits macrophage polarization to M2.

Since the macrophages are mostly derived from bone marrow cells, and also the cytokines up-regulated in trained immunity are pro-inflammatory cytokines. Although the upregulation of inflammatory cytokines after trained immunity of macrophages is determined, no research has studied the polarization of macrophages during this process. Therefore, exploring the polarization of BMDM as an important primary macrophage in trained immunity is very significant and necessary to understand the nature of trained immunity. To determine whether BMDMs are similar to macrophage polarization in PBMCs, we tested the polarization of microphages from male or female mice when challenged with LPS or trained immunity plus LPS. We considered F4/80 + iNOS + BMDMs as M1-type BMDMs and F4/80 + CD206 + BMDMs as M2-type BMDMs. The results demonstrated that female BMDMs are more polarized to M1 in both the LPS group (7.04-5.12%) and TI + LPS group (28.8-17.9%) ( Figure 4A) . Also, male BMDMs began to transform to M2 in 24 h, which did not occur in female BMDMs. Trained immunity also prevented both male and female BMDMs from M2 polarization as well as PBMCs (Figure 4B ).

Macrophage Cell Lines J774 and RAW264.7

In order to examine the effect of estradiol on trained immunity, we decided to pre-treat the macrophage cell lines with estradiol before trained immunity model. Since the concentration of estradiol that can stimulate the macrophage cell lines RAW264.7 and J774 is unknown, we made a concentration gradient of estradiol on the activity of the macrophage cell lines. The results showed that the response of the macrophage cell lines to the stimulation of estradiol is not particularly sensitive, and the viability of J774 begins to increase significantly under the stimulation of 50 nM estradiol. Thus, the concentration of E 2 used in cell experiments was verified as 50 nM (Figures 5A,B) .

The in vitro trained immunity model was established with RAW264.7 and J774 ( Figure 5C ) cell lines derived from male and female mice, respectively. Using TNFα and IL-1β as the marker of inflammation, our data suggested that E 2 can induce stronger trained immunity both in RAW264.7 and J774 (Figures 5D,E) .

We also made a trained immunity model of BMDMs (Figure 6A ). M-CSF was used to induce BMDM with a purity of over 95% from both male and female mice ( Figure 6B) . Then, the mRNA levels ( Figure 6C ) and protein levels ( Figure 6D ) of TNFα and IL-6 were measured. The results suggested that female BMDMs can have a more intensive response to LPS as well as a trained immunity response than male BMDMs. Phosphorylation of Akt and mTOR targets (S6 and 4EBP1) are considered to be key hallmarks of trained immunity (23) . To clarify the effect of E 2 on trained immunity, these hallmarks are checked by western blot, which indicated that E 2 as well as β-glucan induced trained immunity in BMDMS ( Figure 6E ). In addition, the data showed that E 2 further boosted the polarization of M1-type macrophage in trained immunity. Consistently, this effect of E 2 is more apparent in female BMDMs, and E 2 inhibited M2 polarization in trained immunity (Figure 6F ).

NFκB signaling pathway is involved in the regulation of many cellular physiological processes. Previous articles have reported that RelB −/− mice, or inhibiting the nucleus translocation of RelB, led to a higher basal inflammatory level (29, 30) . Other reviews declared that E 2 could regulate nuclear translocation of NFκB through ERs. Since it has been widely studied that TNFα can combine with TNFR on the cell membrane surface to promote NFκB translocate into the nucleus. Also, because TNFα as a representative inflammatory cytokine is secreted by macrophages and will stimulate back to macrophage. We use TNFα as a positive control to study NFκB entry into the nucleus. We use immunofluorescence to explore the intracellular localization of NFκB protein. In immunofluorescence, the results indicated that when TNFα is used to stimulate cells, it does not affect the colocalization of ERα and the nucleus but increases the colocalization area of P65 and RelB with the nucleus. On the contrary, E 2 treatment appeared to induce nuclear positioning of ERα and kept RelB distribution in the cytoplasm in both HEK293T and BMDMs (Figures 7A,B) . However, stimulation of E 2 did not affect the distribution of P65 in cells. Next, we used the RNA interference system to further verify the impact of E 2 on the nuclear translocation of RelB. The silencing performance of interfering small RNA sequence was evaluated both at the mRNA level ( Figure 7C ) and protein level ( Figure 7D) . By extracting nuclear protein, we found that estrogen could reduce the content of RelB protein in the nucleus; by silencing the expression of ERα, the content of RelB protein in the nucleus was also restored ( Figure 7E ). As markers of M2 macrophage polarization, IL-4 and IL-10 are also the downstream genes regulated by RelB (30, 31) . We found that E 2 inhibited the mRNA expression level of IL-10 and IL-4 by regulating nuclear translocation of RelB ( Figure 7F ). In conclusion, these results indicated that E 2 could block RelB translocation to the nucleus; to further inhibit M2-associated gene expression, E 2 suppressed BMDMs M2 polarization.

During the development of sepsis, many systemic organ abnormalities occur including damage to the lung, liver and kidney; the normal operation of the body's neurosensory system may even be affected (32) . Since LPS is a component in the cell wall of gram-negative bacteria, it is wildly used as an ideal stimulus to establish sepsis models. When TLR4 on FIGURE 4 | Female BMDMs are apt to be polarized to M1 phenotype in responses to trained immunity in vitro. (A) Female BMDMs M1 polarization was stronger than male BMDMs treated with LPS or TI + LPS groups. (B) Very few female BMDMs to polarized to M2 in LPS group, while male BMDMs showed the polarization of M2 phenotype. TI suppressed BMDMs to M2 polarization from both male and female mice (n ≥ 3/group). ***p < 0.001, paired Student's t-test comparing LPS group and TI + LPS group in the same gender. # p < 0.05, ### p < 0.001, paired Student's t-test comparing same group between different genders.

the macrophage cell membrane recognizes LPS, a series of signaling pathways will be initiated to stimulate macrophages to produce pro-inflammatory cytokines, which can induce potent systemic inflammatory responses in vivo. Therefore, TNFα, IL-1β, and IL-6 are currently considered to be markers of the early phase of sepsis (33) . The development of sepsis begins with systemic inflammatory response syndrome (SIRS) (34) , which is considered as the early phase of sepsis. Elevated expression of pro-inflammatory cytokines could help the body return to a normal state in early sepsis (35) . After SIRS, the body enters the CARS (compensatory anti-inflammatory response syndrome) stage. In the CARS stage, the immune system will undergo the decline-regulation (36) . The hyper-inflammatory response of SIRS will normally be restored by the subsequent CARS stage. The patients can return to normal state after the CARS stage (37) .

However, if the CARS phase fails, it can cause death from sepsis. As one of the important ways to protect the body from foreign microbes and antigens, the role of trained immunity is very significant. This study focused on the effects of E 2 on early sepsis by promoting trained immunity. In the development of early sepsis, estrogen induced a stronger trained immunity response of macrophages to remove antigens and microorganisms from the body. Simultaneously, estrogen promoted the polarization of macrophages to M1 in vivo and inhibited the polarization of M2, which is considered anti-inflammatory in the early phase of sepsis. In summary, estrogen can maintain the higher proinflammatory state of macrophages. This also illustrates the reason why females are more tolerant to sepsis than males in one aspect. However, further research is needed to understand the role of estrogen in the later stages of sepsis. The mRNA levels of TNFα and IL-1β in RAW264.7 were detected by qPCR to determine the trained immunity effect with or without E 2 (n ≥ 3/group). # p < 0.05, ### p < 0.001, paired Student's t-test comparing β-glucan + LPS group and LPS group. *p < 0.05, ***p < 0.001, paired Student's t-test comparing with control group. ∧p < 0.05, ∧∧p < 0.01, and ∧ ∧ ∧p < 0.001, paired Student's t-test comparing between β-glucan + LPS groups with or without E 2 . Here, we demonstrated that β-glucan-induced trained immunity was more resistant to sepsis in female than male mice. OVX mice manifested serious sepsis consequences with a weaker trained immunity effect than female mice. Macrophage polarization toward M1 phenotype is thought to exhibit the enhanced trained immunity. E 2 promoted trained immunity in vitro and in vivo. Inhibition of E2 on the nucleus translocation of RelB contributed to macrophage polarization to change the intensity of trained immunity. Our results indicated that E 2 is involved in the trained immunity in gender differences.

Since trained immunity was discovered in 2014, although there are many articles about trained immunity, there is no article to find the fundamental way of trained immunity activation but only about the changes of immune cell characterization after trained immunity activation. Such as epigenetic changes, upregulation of glycolysis, autophagy level, Akt phosphorylation, and so on. In this study, we found that E 2 promotes trained immunity by suppressing RelB entry into nucleus, while inhibiting macrophage polarization to M2 in inflammation (A way reverse the inflammatory response). It is possible that E 2 can change the epigenetics of macrophages through estrogen receptors to affect the trained immunity. This hypothesis needs further researches.

Trained immunity is a way of immunization that occurs in the innate immune cells through the first stimulation to fight the later secondary infections. By obtaining trained immunity, the body can fight various infections from bacteria, fungi and even viruses timely. It is worth mentioning that in countries and regions with underdeveloped scientific research capabilities, it may be an economical and quick means of protection against Covid-19 to enhance people's trained immunity ability. Sepsis is a clinically common infectious disease with obvious gender differences. In this article, sepsis model is used as an infection model to evaluate the role of estradiol in enhancing trained immunity. The mechanism and effects of estradiol in promoting trained immunity also need subsequent study in other types of infectious diseases.

The purpose of this paper was to explore the reasons why different genders have different tolerance effects on sepsis. An article reported that estradiol and DHT (dihydrotestosterone) did not influence BCG-induced trained immunity, and the article only focused on the inflammatory cytokines of monocytes induced by BCG in vitro (22) . Apart from this, almost no articles study the effects of E 2 on trained immunity and its biological significance. Our research attempted to explain its effects on trained immunity and understand how it causes women to be more tolerant of sepsis than men. However, in terms of gender differences, many factors, such as androgen concentration, genetic differences, metabolic differences, and physiological differences may all be the result of different tolerances for sepsis between genders (12, 38, 39) . Gender differences are a very complex and exquisite scientific issue (40) , and all of the factors that contribute to gender differences are worth exploring for subsequent experiments.

In summary, we demonstrated that as one of the key factors for gender differences, E 2 plays a vital role in the stronger tolerance of females to sepsis than males. One the one hand, E 2 can better facilitate trained immunity by increasing expression of inflammatory cytokines and inducing macrophage M1-type polarization; on the other hand, E 2 can inhibit or delay the macrophage M2-type polarization by regulating nucleus translocation of RelB and its down-stream M2-associated genes. Thus, this may provide a new idea for the clinical treatment of sepsis. Drugs with a structure similar to estrogen may be developed to treat sepsis. More importantly, the treatment of some diseases may able to find better solutions by addressing the different characteristics of different genders.

The datasets generated for this study are available on request to the corresponding author.

The animal study was reviewed and approved by Model Animal Research Center of Nanjing University.

All authors reviewed the manuscript, contributed to data analysis, drafting and revising the article, gave final approval of the version to be published. ZS conceived and designed the project. ZS, YP, JQ, and YX participated in the animal experiments. ZS and JQ wrote the manuscript. YH and YX revised it. 

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The authors appreciate the warm-hearted help from all the co-authors and the professor.