CD81+ fibroblasts, a unique subpopulation with accelerated cellular senescence, exaggerate inflammation and activate neutrophils via C3/C3aR1 axis in periodontitis

  1. Liangliang Fu
  2. Chenghu Yin
  3. Qin Zhao
  4. Shuling Guo
  5. Wenjun Shao
  6. Ting Xia
  7. Quan Sun
  8. Liangwen Chen
  9. Min Wang
  10. Haibin Xia

  • Curated by eLife

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    eLife assessment

    This useful study identifies a population of CD81-positive fibroblasts showing senescence signatures that can activate neutrophils through the C3/C3aR1 axis, hence contributing to the inflammatory response in periodontitis. Solid evidence, combining in vitro and in vivo analyses and mouse and human data, supports these findings. The work could be of interest to researchers working in the senescence and oral medicine fields

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Abstract

Periodontitis, a prevalent inflammatory disease worldwide, poses a significant economic burden on society and the country. Despite numerous studies, the biological molecular mechanism underlying the development and progression of periodontitis remains unclear. Previous research has established a connection between cellular senescence and periodontitis. However, the role and mechanism of cell senescence in the progression of periodontitis have not been thoroughly investigated. This study aimed to explore the involvement of cellular senescence in the pathogenesis of periodontitis and determine the underlying mechanisms. Our findings demonstrated that senescent cells accumulated during the periodontitis progress and inhibiting cellular senescence in periodontitis via administration of metformin successfully alleviated inflammation and bone loss. Moreover, several scRNA-seq analysis suggested that gingival fibroblasts were the main cell population undergoing cellular senescence during periodontitis, which helps mitigate tissue damage and bone loss. Furthermore, we identified a high expression of CD81 in the senescent gingival fibroblast population. These cells were found to actively contribute to inflammation through their potent pro-inflammatory metabolic activity and secretion of SASP-related factors. Additionally, they recruited neutrophils via the C3/C3aR1 pathway, indirectly sustaining the inflammatory response. These results provide valuable insights into the cellular and molecular basis of periodontitis-induced tissue damage, highlighting the significance of fibroblast senescence. In conclusion, our study sheds light on the relationship between CD81 and cellular senescence, suggesting its potential as a therapeutic target for periodontitis.

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  1. Version published to 10.7554/elife.96908.1 on eLife
  2. Version published to 10.7554/elife.96908 on eLife
  3. eLife

    eLife assessment

    This useful study identifies a population of CD81-positive fibroblasts showing senescence signatures that can activate neutrophils through the C3/C3aR1 axis, hence contributing to the inflammatory response in periodontitis. Solid evidence, combining in vitro and in vivo analyses and mouse and human data, supports these findings. The work could be of interest to researchers working in the senescence and oral medicine fields

  4. eLife

    Reviewer #1 (Public Review):

    Summary:

    In this manuscript, Liangliang Fu and colleagues propose that a population of CD81-positive fibroblasts exhibiting senescent features activate neutrophils via the C3/C3aR1 axis and contribute to maintaining the inflammatory response in periodontitis. The authors provide evidence that inhibition of cellular senescence by metformin treatment in murine models ameliorated periodontitis progression. This study provides some valuable insights into the impact of periodontitis-induced gingival damage and the significance of stromal senescence.

    Strengths:

    (1) The work combines a variety of models of periodontitis, including analyses of human samples, primary gingival fibroblast cell culture isolation and cultures, and mouse models of ligature/induced periodontitis. Then, the results are solid in terms of used models.

    (2) Comprehensive exhibition of methodologies incorporating histology procedures, micro-CT imaging, bulkRNAseq and scRNAseq transcriptomic profiles (the latter analyses of published datasets), and a number of computational analyses. The paper is robust at the technical level.

    (3) This paper is timely and interesting and it opens potential therapeutic avenues for the treatment of periodontitis. Although the interplay of senescence with periodontitis and the use of metformin has been previously reported (e.g. Kuang et al. Biogerontology 2020), I think the proposed mechanism of neutrophils activation by CD81-positive senescent fibroblasts and the inflammatory response is original. The paper is therefore at the forefront of the field, as senescence and its interplay with the immune system is a hot topic and reflects the current directions ("trending topics") of the field.

    Weaknesses:

    (1) The assessment of Cellular Senescence is limited and would benefit from additional biomarkers and not just p16 and p21, in particular in vivo.

    (2) This paper does not include original scRNAseq datasets in periodontitis, but analyses of already published datasets.

    (3) The authors claim that cellular senescence of CD81+ fibroblasts could be attributed to disturbances of lipid metabolism, resulting in differentiation arrest and higher expression of SASP factors in CD81+ fibroblast cells. Although the authors found that a series of pathways related to metabolism (metabolism of linoleic acid, linolenic acid, arachidonic acid, or steroid biosynthesis) are upregulated in CD81+ fibroblasts by transcriptomic analyses the hypothesis remains speculative and requires further validations.

    (4) Metformin has been reported to downregulate the SASP and lower senescent cell burden (e.g. for review see Kulkarni, Gubbi, and Barzilai. Cell Metab 2020). Although Metformin's senotherapeutic activities can be mediated by anti-inflammatory effects preventing NFkB translocation to the nucleus (Moiseeva et al. Aging Cell 2013) and has been shown to prevent oxidative stress-induce senescence in human periodontal ligament cells (Kuang et al. Biogerontology 2020) it can also drive multiple and pleiotropic effects unrelated to senescence.

    (5) Mechanistically, the proposed activation neutrophils by senescent C81+ fibroblasts via the C3/C3aR1 axis would be further supported by using a senolytic approach (e.g. Bcl2 inhibitor) allowing testing of whether eradication of senescent stromal cells results in reduced levels of CD81 and C3 positivity, and prevention of neutrophils infiltration.

  5. eLife

    Reviewer #2 (Public Review):

    Summary:

    The authors report the discovery of a population of gingival fibroblasts displaying the expression of cellular senescence markers P21 and P16 in human periodontitis samples and a murine ligature-induced periodontitis (LIP) model. They support this finding in the murine model through bulk RNA-sequencing and show that differentially expressed genes are significantly enriched in the SenMayo cellular senescence in an aging dataset. They then show that Ligature-Induced Periodontitis (LIP) mice treated with the senomorphic drug metformin display overall diminished bone damage, reduced histomorphic alterations, and a reduction in P21 and P16 immunostaining signal. To explore the cell types expressing cellular senescence markers in periodontitis, the authors make use of a combination of bioinformatic analyses on publicly available scRNA-seq data, immunostainings on patient samples and their LIP model; as well as in vitro culture of healthy human gingival fibroblasts treated with LPS. They found that fibroblasts are a cell population expressing P16 in periodontitis which are also enriched for SenMayo genes, suggesting they have a senescent phenotype. They then point to a subgroup of fibroblasts expressing CD81+ with the highest enrichment for a SASP geneset in periodontitis. They also show that treatment of LIP mice and human LPS-treated gingival fibroblasts with metformin leads to a reduction of P21 and P16-positive cells, as well as the senescence-associated beta-galactosidase (SA-beta-gal) marker. Finally, they show evidence suggesting that CD81+ senescent fibroblasts are the source of C3 complement protein, which they stipulate signals through the C3AR1 receptor present in neutrophils in periodontitis. The authors observed that both CD81+ fibroblast and C3AR1+ neutrophil populations are expanded in periodontitis, that both populations appear to be in close contact, and that treatment with metformin reduced both C3 and the neutrophil marker MPO in their mouse LIP model.

    Strengths:

    The study implements several different techniques and tools on human samples, mouse models, fibroblast cultures, and publicly available data to support their conclusions. In summary, the evidence suggests that in the context of periodontitis, there is an expansion of cells expressing senescence markers P21, and P16, as well as members of the SASP, and that this includes CD81+ fibroblasts.

    Weaknesses:

    The manuscript appears to use as synonyms the terms "senescent cells" and "aging cells", as well as "senescence" and "aging", or "accelerated senescence" and "accelerated aging". This choice of words makes it difficult to understand the objectives of the study and the interpretations the authors are deriving from their results. The current understanding of the role of cellular senescence is that it is only one of the multiple biological aspects that characterize physiological aging. Although deeply intertwined, aging and cellular senescence are widely considered distinct phenomena, but the difference between these concepts seems blurry to me within the manuscript.

    After reading the manuscript, my understanding is that the authors are comparing the process of periodontitis to a form of accelerated aging, in which senescent cells are potential drivers or contributors. I believe this to be an interesting point of view. As the authors mention, periodontitis is more common in the elderly, and senescence is strongly implicated in aging. However, I am not entirely sure if the authors were trying to address such a question, and more importantly, the experiments conducted here cannot address the relationships between cellular senescence in periodontitis and aging as (1) they do not conduct an expanded analysis of molecular and cellular features of aging in the oral epithelium beyond cellular senescence, (2) they do not test this hypothesis in vitro and in vivo using models of accelerated or delayed aging (or publicly available datasets of such models), and (3) interpretations regarding the aging process are hindered by the fact that all human healthy patients were young adults, while all human periodontitis patients were middle-aged, while the mouse model did not include different age groups.

    The authors also refer to metformin as an "anti-aging" drug. Therefore, to me, it is not clear if the authors intended to use metformin as a senotherapeutic agent to show a correlation between senescence markers and the severity of periodontitis, or if they conceived their experiments and interpreted their results as "delaying the aging process". The latter would be more difficult to determine as cellular senescence is only one of the several aspects of the aging process in tissues. As none of the other molecular and cellular hallmarks that characterize the process of aging (epigenetic alterations, telomere shortening, immunosenescence, mitochondrial dysfunction, stem cell depletion, genomic instability, loss of proteostasis, nutrient sensing disruption, etc.) were studied, I believe this might be just a matter of semantics and rephrasing.

    On the other hand, and assuming the authors were only seeking to explore the role of cellular senescence in periodontitis (irrespective of the aging process), I have the following concerns:

    Major concerns:

    (1) A majority of the bioinformatic analyses regarding cellular senescence were conducted using only the SenMayo geneset reported by Dominik Saul et al. That geneset was developed by literature searching for genes associated with cellular senescence that had been studied in the context of human aging (in bone marrow). Thus, my understanding is that it is not an "aging" gene set as the authors describe it (and possibly interpret it) throughout the manuscript but a gene set of cellular senescence-associated genes that are overrepresented in aging tissues.

    The SenMayo geneset specifically excludes important genes like P21, P16, and RELA as they were used for validating that dataset against other datasets. Additionally, most of the genes that comprise SenMayo are cytokines and growth factors. This includes part of the SASP (and the authors also show enrichment for some SASP factors using the Coppé dataset in Figure 5) but excludes many of the core important processes that are known to define cellular senescence, including cell cycle inhibition, lack of cell proliferation, accumulation of DNA damage, activation of the lysosomal compartment and disruption of the nuclear envelope, among others. As the SenMayo geneset was developed for studying senescence in the context of aging, I believe it is important to conduct a more extensive analysis with other published gene sets of cellular senescence. Examples include the cellular senescence and SASP REACTOME pathways, the KEGG cellular senescence pathway, the cellular senescence GO term, the Fridman dataset, SeneQuest, CSGene, CellAge, etc. Most importantly, it will be important to show the enrichment of pathways related to hallmark pathways underlying cellular senescence such as cell cycle inhibition, the DNA damage response and repair pathways, NF-kB signaling, MTOR, and autophagy signaling, etc. Showing the enrichment level of these pathways in the CD81+ fibroblasts in periodontitis would be of utmost importance for backing up the conclusions of this study.

    (2) The most important aspect of the definition of cellular senescence is the absence of cell proliferation. Beyond the expression of the p21, p16, and SASP markers, any evidence showing that CD81+ fibroblasts are not proliferating in vivo in humans and mice, and in vitro in the case of LPS experiments, would be of great importance for defining these cells as senescent. Otherwise, conclusions should be toned down to refer to the expression of senescence markers or cells having a "senescent-like" phenotype.

    (3) The use of a "relative optic density" metric instead of positive cell counts as a measure for quantifying IHC stainings might pose challenges in reproducing these results, especially for the P21 and P16 stainings which are proteins that despite being possibly also being found in the cytoplasm, should be clearly present in the nucleus of positive cells. The quantification of the levels of these markers is of great importance for the conclusions of this study but I am concerned they would be too difficult to reproduce. In my opinion, cell counts and % of positive cells should be used, with a clear description of the total number of cells counted in the methodology. Otherwise, a strong justification for using OD in the methodology is required in addition to considering the following comments:

    a. There is no description in the methodology describing how this relative OD is measured and calculated. It is not clear if the data points shown in the graphs are biological replicates or OD means measured in different histological sections from the same sample.

    b. The images of P16 and P21 stainings in Figures 2E and 2F do not appear to resemble the differences in OD between conditions shown in the graphs of Figures 2Gd and 2Ge.

    c. The stainings shown for p16 in Figure 2E seem considerably different from those shown in Figure 1D. Additionally, the relative OD of P16 at 14D is around 0.08 in Figure 1D, while the mean for the control appears to be around 0.015 at 14D in Figure 2Gd. The use of OD as a measure is again worrying as this could be impacting interpretations: the difference between the ODs of LIP+MET (around 0.08) and LIP+ddH2O (around 0.015) is reported as significant but the difference in OD between LIP14D in Figure 1D (around 0.07) and LIP+ddH2o in Figure 2Gd (around 0.015) should not be significant as they are supposed to similar control conditions.

    d. Irrespective of the measure used, the authors should state exact means and standard deviations, as well as exact P values, the statistical test used, and the number of biological replicates per group in parenthesis in the main text and figure legend.

    (4) The conclusions derived from experiments with metformin in mice and cell cultures are not fully supported by the evidence.

    First, metformin has multiple molecular targets, as well as multiple organ and tissue targets. The experiments presented in mice do not consider/evaluate the systemic effects of metformin nor local effects in other gingival cell types and this should be discussed.

    As mentioned before, these experiments cannot be interpreted as testing metformin in the context of "anti-aging", as this study addresses cellular senescence in periodontitis. However, the results are still relevant as there is considerable evidence showing that metformin has senomorphic activity. In this regard, the authors could make use of a compound that has been more extensively characterized as a senolytic such as ABT-737, ABT-263 (Navitoclax), or the combination of Dasatinib + Quercetin, to show the effect of eliminating senescent cells in their LPS induction fibroblast model.

    They could also show the effect of metformin on the activation of other hallmark senescence pathways such as (the NF-kB pathway or the DNA damage response) and in the expression of SASP factors they identified as overexpressed in CD81+ fibroblasts through their analysis against the SenMayo dataset (e.g., IL6, CXCL1, CXCL12). This could be done in their samples from metformin-treated mouse experiments and in their LPS induction fibroblast model.

    (5) For the data produced on the authors' human samples, the difference in the age of patient groups is a significant confounding factor. This is because all their periodontitis patient samples came from middle-aged individuals (mean age above 50 years), while all healthy samples were obtained from young adults (mean age 25 years). The authors should justify this selection of age groups and justify why differences in the age of each experimental group could impact the validity of their results regarding the accumulation of senescent cells. Showing the level of P21 and P16 positive cell accumulation in samples from healthy patients from a similar age group (middle-aged) is of great importance to support the validity of their results in humans.

  6. eLife

    Reviewer #3 (Public Review):

    Summary:

    This work investigates the role of cellular senescence in the progression of Periodontitis using a combination of in vivo and in vitro mouse modelling experiments, human periodontitis samples, and transcriptomic analyses.

    The authors propose that gum fibroblasts from either patient periodontitis samples or a mouse model of periodontitis can enter a state of cellular senescence (Figure 1). Treatment of their periodontitis mouse model with the compound Metformin attenuated this senescent phenotype and mildly reduced symptom severity. Therefore providing a potential mechanistic link between the senescent state and disease progression (Figure 2).

    Leveraging analysis of published single-cell RNA-sequencing datasets of human healthy and periodontitis gum samples, the authors identify CD81+ gum fibroblasts as the cell type with the greatest enrichment of senescence-associated gene expression (Figures 3 and 4) as well as possessing metabolic alterations (Figure 5). Finally, the authors propose that these senescent gum fibroblasts are able to recruit neutrophils through C3 signalling, generating a sustained inflammatory environment that promotes disease progression (Figure 6).

    The conclusions of this research are mostly well supported by that data. However, the characterisation of the senescent state and its causal involvement in disease progression could be further improved.

    Strengths:

    (1) The authors' use of both human and mouse samples provides important translational relevance to their research by finding analogous populations of putatively senescent fibroblasts in both systems.

    (2) The use of single-cell RNA-sequencing datasets derived from patient control and periodontitis samples provides a powerful system for interrogating specific cell types. Such an analysis allowed for the characterisation of fibroblast heterogeneity revealing the unique CD81-expressing subset as having the greatest senescent characteristics. Importantly, this result was validated by immunofluorescence in both mouse and human periodontitis systems.

    Weaknesses:

    (1) The assessment of cellular senescence induction during periodontitis is rather superficial, relying on p16 and p21 Immunohistochemical staining and geneset enrichment analysis (Figure 1). This could be bolstered by their in vitro human fibroblast culture system utilising LPS stimulation. Specifically, their assessment could be more robust by including further markers of senescence such as (i) expression of DNA-damage markers, (ii) evidence of proliferative arrest, and (iii) assessment of an induced secretory phenotype. While a SASP signature was defined in Figure 5A, this was derived from a published single-cell RNA-sequencing dataset. Finding an analogous SASP signature in their human fibroblast cultures/bulk RNA-sequencing comparison of mouse normal-versus-periodontitis tissue would provide more compelling evidence for senescence induction.

    (2) While Metformin treatment has an existing basis in the literature as a therapeutic strategy for treating periodontitis, the authors of the current study provide novelty by proposing that Metformin acts by reducing the senescent cell burden during periodontitis. While Metformin treatment is able to significantly reduce the severity of bone damage in ligation-induced periodontitis, the effect is quite mild and the evidence presented does not compellingly show an effect on the putatively senescent p16+ and p21+ cell populations in the gum (Figures 2E and F). Moreover, while the authors show that Metformin treatment is able to attenuate senescence by reducing the expression of senescence-associated Beta-galactosidase (Supplementary Figure 2E), this raises several questions. Namely, (i) Does Metformin prevent the acquisition of a senescent state or (ii) is it acting as a senolytic by actively killing the senescent fibroblasts? It would be important to address these questions to better assess whether Metformin treatment is efficacious only prophylactically, or whether it can have an effect during disease progression. Furthermore, experimental testing if other, widely utilised, senolytics strategies (i.e Navitoclax, Dasatinib+Quercetin, Fisetin etc...) or testing if a p16-/- genetic background is able to attenuate senescence and produce similar protective response would provide more compelling evidence to support their conclusion that cellular senescence is having a causal role in disease progression.

    (3) The authors' metabolic profiling of their senescent gum fibroblasts, through interrogation of the transcriptomic datasets, reveals an upregulated synthesis of arachidonic acid. Through this they propose that it can be converted into prostaglandins and leukotrienes, by COXs expressed by the fibroblasts, fuelling tissue inflammation. However, this mechanism promoting inflammation is speculative and lacks experimental demonstration. To support this mechanism it would be important to show (i) increased prostaglandin/leukotrienes expression in periodontitis (relative to healthy control) and (ii) the ability to reduce this by attenuating the senescent phenotype (either by Metformin or other senolytics strategies).

  7. Version published to 10.1101/2024.02.21.581332v1 on bioRxiv