Encyclopedia
Please note this is a comparison between Version 1 by Patrícia Elaine de Almeida and Version 2 by Lindsay Dong.
Extracellular vesicles (EVs) have a significant impact on the pathophysiological processes associated with various diseases such as tumors, inflammation, and infection. They exhibit molecular, biochemical, and entry control characteristics similar to viral infections. Viruses, on the other hand, depend on host metabolic machineries to fulfill their biosynthetic requirements. Due to potential advantages such as biocompatibility, biodegradation, and efficient immune activation, EVs have emerged as potential therapeutic targets against the SARS-CoV-2 infection.
- extracellular vesicles
- lipid bodies
- COVID-19
1. Introduction
Respiratory viral diseases are a significant threat to human life and have been demonstrated to elevate pandemic risks, which is primarily due to their intricate transmission dynamics and viral evolutionary processes. In this context, the COVID-19 pandemic represented a significant global challenge. The etiological agent was identified as a novel coronavirus, named Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), and the disease it causes was termed coronavirus disease 19 (COVID-19) [1]. It is now known that SARS-CoV-2 primarily spreads through respiratory droplets and aerosols generated by activities such as speaking, coughing, and sneezing [2][3][4][5][2,3,4,5].
Viruses and their hosts have undergone coevolution over an extended period, resulting in selective pressure on both the pathogen and the human immune system. On one hand, the immune system has adapted to counter viruses and infected cells, while viruses have developed intricate mechanisms to evade the immune response [6][7][8][9][10][11][11,12,13,14,15,16]. These pathogens manipulate host lipid metabolism to evade the immune system, promote their replication or trigger pathological responses [12][13][17,18]. Focusing on the interplay between SARS-CoV-2 and host lipid metabolism shows potential for the development of therapeutic strategies [12][17]. Despite the utilization of cellular organelles like lipid droplets (LDs), viral proteins, either independently or in concert with hijacked host proteins, swiftly alter the protein and lipid composition, as well as the structure, of LDs to achieve optimal conditions for replication [14][19]. Moreover, following replication and the assembly of new viral particles, (+) ssRNA viruses can commandeer membranes as carriers for non-lytic cellular exit, facilitating transmission to other susceptible hosts [14][19].
SARS-CoV-2 infection induces the formation of cytoplasmic membrane-bound vacuoles in respiratory epithelial cells, which are able to carry on virus-like particles. Both healthy and virally infected cells release EVs, which indeed serve as potential targets for the mediators of viral infection [15][16][17][20,21,22]. The action of EVs is mostly associated with their content, dependent on the state of homeostasis, as well as the cells of origin [18][23]. EVs are membrane-enclosed structures containing various biomolecules such as proteins, miRNAs, mRNAs, long non-coding RNAs (lncRNAs), DNA strands, lipids, and carbohydrates derived from their parent cells. Thus, they are capable of delivering these biomolecules to target cells, thereby reprogramming their metabolism, function, and morphology [19][20][21][24,25,26].
Increasing evidence underscores the crucial roles of secreted vesicles in the pathogenesis of several human diseases, notably cancer, neurodegenerative disorders and infections. The possible role of the EVs in incorporating pathogen-derived materials and becoming delivery vectors was described by Gould et al. in 2003 as the “Trojan exosome hypothesis” and was adapted in 2014 by Izquierdo-Useros N [22][23][27,28]. Over the past 40 years, scientists have explored the relationship between viral pathogenesis and exosomes [24][25][29,30].
A prominent characteristic of SARS-CoV-2 infection involves the utilization of host cell membranes to generate replication organelles, exhibiting a spectrum of morphologies encompassing double-membrane structures and vesicular compartments. These organelles fulfill the function of safeguarding viral RNA from the host innate immune system sensors, thereby contributing to viral evasion mechanisms [26][27][28][38,39,40] (Figure 1).
Figure 1. The SARS-CoV-2 infection cycle and the production of EVs. There are two distinct SARS-CoV-2 entry pathways. (1) CD9 works with TMPRSS2 to cleave viral fusion glycoproteins, facilitating coronavirus entrance. Alternatively, the virus binds to the ACE2 receptor in the lipid rafts region, where the virus–ACE2 complex is internalized via endocytosis. (2) The infection with a coronavirus causes the creation of new membrane structures of various sizes and forms in the perinuclear area, which are collectively referred to as replication organelles. Viral structural proteins and genomic RNA are produced at the replication site and subsequently translocated to the ER-Golgi intermediate compartment (ERGIC), where virus assembly and budding occur via an unknown mechanism. New viruses from the ERGIC lumen bud into the secretory route and reach the plasma membrane, where they are released into the extracellular environment after virus-containing vesicles fuse with the plasma membrane. In parallel, (3) SARS-CoV-2 arrives at lysosomes via the late endosome and (4) multivesicular bodies (MVBs), forming exosomes containing viral cargo (5), which are released into the extracellular environment. In parallel, EVs can be internalized by clathrin-mediated endocytosis (6). In detail, EVs carry proteins such as MHC, Tetraspanin, ACE2 and flotillin on their membrane while also containing viral and host cell components internally.
2. EVs Origins, Secretion and Communication
EVs are traditionally classified based on their size and mode of release from the cell. These vesicles are referred to by various names including exosomes, microvesicles (ectosomes), microparticles and apoptotic bodies (oncosomes). Exosomes are small EVs (40–100 nm) that bud from multivesicular bodies (MVBs) within cells and are released upon fusion of the MVBs with the cell plasma membrane, releasing their intraluminal vesicles in the extracellular environment in the form of exosomes [29][30][31][32][44,45,46,47].
EVs’ biogenesis is regulated by ceramide synthesis at the plasma membrane and endosomal levels [33][34][48,49]. The inhibition of neutral sphingomyelinase (nSMase) in both human and animal cells suppresses the release of exosomes while significantly boosting the release of microvesicles from the plasma membrane [34][49]. There are several proteins involved in exosome biogenesis such as endosomal sorting complex required for transport (ESCRT), vacuolar ATPase, and Vps4, which segregate and sort ubiquitylated proteins into intraluminal vesicles [19][35][36][37][38][39][8,24,50,51,52,53].
Microvesicles or ectosomes, on the other hand, are larger EVs (200–500 nm) believed to bud directly from the plasma membrane [32][40][41][47,54,55]. Similar to exosomes, the generation of microvesicles involves the active participation of several protein factors. These factors encompass Ca2+-dependent aminophospholipid translocases, namely flippases and floppases, sphingomyelinase 2 (nSMase2), scramblases, and calpain. They collectively orchestrate the rearrangement of phospholipids, membrane curvature, and actin cytoskeleton reorganization, ultimately resulting in the extracellular formation of microvesicles [42][43][44][45][56,57,58,59]. Apoptotic bodies or oncosomes are fragments of cells undergoing programmed cell death, representing the largest EVs with a diameter ranging from 1 to 5 μm [32][41][42][46][47,55,56,60].
EVs from eukaryotic cells play a vital role in both local and systemic cellular communication, serving as intracellular mediators upon release into the extracellular space [21][26]. Since EVs have the same membrane orientation as cells, they expose on their surface the extracellular domains of transmembrane proteins that can bind to nearby or long-distance targets. These EVs transfer their bioactive cargo to target cells, thereby influencing and altering their behaviors [47][61].
The uptake of EVs is influenced by several factors, encompassing their dimensions, surface composition (lipids, glycans, proteins), pH conditions, temperature, and oxidative/hypoxic environment [35][8]. The nature of both the donor and recipient cells can modulate this process [48][63]. EVs are secreted through exocytosis or in multivesicular endosomes (MVEs), and they interact with target cells through ligand/receptor signaling at the plasma membrane [21][26]
The cargo of EVs, which includes lipids, DNA, RNA and proteins, can alter the transcription and signaling activity of recipient cells, thereby regulating their phenotype and function [35][8]. The protein composition of various types of EVs largely reflects that of the parent cells, exhibiting a notable enrichment of specific molecules. These include adhesion molecules, membrane-trafficking proteins, cytoskeleton components, heat-shock proteins, cytoplasmic enzymes, signal transduction molecules, cytokines, chemokines, proteinases, and cell-specific antigens [49][66]. They originate from both immune and non-immune cells, which play a vital role in immune system regulation. EVs also possess the capacity to either facilitate immune stimulation or suppress it, thereby influencing the development of inflammatory, autoimmune, and infectious diseases.
3. EVs as Potential Role for Immune System Evasion during SARS-CoV-2 Infection
Viruses have developed intricate strategies to counteract the innate immune response, including interfering with antigen presentation, disrupting interferon signaling, and producing “decoy” sub-viral particles that bind to neutralizing antibodies (nAbs), thereby reducing their effective concentration available for neutralizing infectious virions [6][7][8][9][10][11][11,12,13,14,15,16]. The virions consist of a structural spike glycoprotein, an M-membrane protein (a type III transmembrane glycoprotein), an N-nucleocapsid protein (present within the phospholipid bilayer), and non-structural proteins [50][51][76,77]. Approximately one-third of the RNA sequence encodes four fundamental structural proteins: spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins. The remaining two-thirds of the viral genome consists of ORF1a and ORF1b, which encode non-structural replicase/transcriptase proteins [52][78]. SARS-CoV-2 enters the host through the respiratory tract and infects the cell mainly via the angiotensin-converting enzyme 2 (ACE2) receptor. ACE2 is a type I integral membrane protein involved in the renin–angiotensin system, which is found in the kidney, testis, intestine, lung, retina, cardiovascular system, adipose tissue, and central nervous system [53][80]. Once SARS-CoV-2 is internalized into the cell cytoplasm, its lipid bilayers are dismantled by lysosomal enzymes. Subsequently, SARS-CoV-2 utilizes the host cell’s RNA polymerase to replicate its viral single-stranded RNA, thereby increasing the viral load within the host cell [54][81] (Figure 1). The SARS-CoV-2 pathogenicity is highlighted by the entry of the virus through ACE2 receptors, cleavage of the complex, and activation of the S-protein by TMPRSS 2 [55][82]. According to structural analyses, the spike protein of SARS-CoV (SARS-S) contacts the apex of subunit I of the ACE2 catalytic domain. Once attached to ACE2 by SARS-CoV, the ectodomain of ACE2 is cleaved, which is accompanied by endocytosis of the transmembrane domain into the cell and sometimes internalized as an intact molecule [56][83]. The internalization and virus particle–host cell fusion is essential for virus entry [57][84] (Figure 1). In the pathogenesis of COVID-19, cells that express ACE2 and CD9 can transfer these viral receptors to other cells via EVs, making recipient cells more susceptible for SARS-CoV-2 infection. Recent investigations have shed light not only on the presence of ACE2 within EVs but also on the capacity of the EVs to transfer ACE2 across various cell types [58][85]. In this context, SARS-CoV-2 gains access to target cells through binding to exosomal ACE2. However, recent studies have underscored the virus’s strong dependence on endocytic mechanisms with the ability to undergo swift endocytosis in cells that express high levels of ACE2 [59][86] (Figure 1). Hence, an alternative mechanism for EV-mediated viral entry involves one of the most highly expressed surface proteins on EVs, tetraspanin CD9 [60][75]. Research has indicated that CD9 collaborates with TMPRSS2 in cleaving viral fusion glycoproteins, expediting the entry of coronaviruses [61][74], such as MERS-CoV [62][87], into lung cells. These findings suggest that CD9 and other tetraspanins on the exosomal surface may serve as mediators in SARS-CoV-2 infection [61][74] (Figure 1). Many factors have been associated with both altered ACE2 expression and COVID-19 severity and progression, including age, sex, ethnicity, medication, and several comorbidities, such as cardiovascular disease and metabolic syndrome. Although ACE2 is widely distributed in various human tissues and many of its determinants have been well recognized, ACE2-expressing organs do not equally participate in COVID-19 pathophysiology, implying that other mechanisms are involved in orchestrating cellular infection, resulting in tissue damage [61][74]. Thus, one of the immune evasion strategies employed by SARS-CoV-2 involves the release of exosomes [63][88], which can carry viruses, viral proteins, and genetic material. Many studies have suggested the role of released SARS-CoV-2-loaded exosomes and other EVs as potential mechanisms for COVID-19 infection relapse [25][64][30,89]. The composition of plasma exosomes varies with the severity of the disease, with mild disease-associated vesicles modulating antigen-specific CD4 T cell responses and severe disease-associated vesicles linked to chronic inflammation [65][90]. Therefore, analyzing exosome components provides valuable insights into different disease states. The virus co-opts the host’s lipid metabolism to optimize its replication dynamics. By targeting the host cells’ LDs, the principal reservoir of neutral lipids, the SARS-CoV-2 acquires energy substrates crucial for supporting its replication cycles [12][17] (Figure 2).Figure 2. SARS-CoV-2 infection induces lipid droplet formation. (1) SARS-CoV-2 infection, via ACE2 receptor, can increase the activation of important transcription factors, such as SREBP1 and PPAR-gamma, leading to an increased induction of LDs biogenesis and the production of eicosanoids which modulate the host’s immune response. (2) EVs containing viral cargo are released into the extracellular environment. (3) Virus utilie the ER machinery for replication. (4) LDs interact with virus and support SARS-CoV-2 replication (box). Pharmacological inhibition and the genetic knockdown of SREBPs and DGAT1 inhibitor (A922500) can reduce SARS-CoV-2 replication and LD biogenesis. In detail, viral particles interact with LD, which is exhibiting structural proteins, such as PLIN-1, PLIN-2 and PLIN-3, and viral RNA. AA, arachidonic acid; COX-2, cyclooxygenase; DAG, diacylglycerol; PGE2, prostaglandin E2; TAG, triacylglycerol.
4. Impact of SARS-CoV-2 Infection in the Cellular Lipid Metabolism
Recent data suggest that lipid domains, known as lipid droplets, play an important role in SARS-CoV-2 replication and the synthesis of inflammatory mediators during the disease as well as in other viral infections such as dengue HCV, DENV, and rotavirus.
The virus’s cellular tropism for lipid metabolism cell machinery suggests that the virus may exploit endogenous lipid materials of different forms, such as lipoproteins and exosomes, as “Trojan horses” to facilitate immune evasion in their systemic spreading [28][40].
LDs are intracellular structures that contain triglycerides, cholesterol esters, and enzymes involved in lipid synthesis and storage (Figure 2, box). The expression of proteins linked with lipid metabolism and de novo lipid synthesis is modified during SARS-CoV-2 infection, as well as the pathways involved in lipid uptake, such as CD36 and the primary transcriptional factors involved in lipogenesis, including (peroxisome proliferator-activated receptor) PPARγ and SREBP-1 (Figure 2) [12][66][17,102].
SREBP is a transcription factor family that regulates lipid homeostasis by directing the expression of a wide range of fatty acid (SREBP1) and cholesterol (SREBP2) metabolic enzymes [66][102]. SREBP isoforms have been shown to increase during SARS-CoV-2 infection. Their activation is linked to the immunological response via the increased assembly of the inflammasome complex, which results in the production of IL-1 [67][103].
Beyond their direct role in viral replication, LDs have also been associated with the establishment of a pro-inflammatory state in COVID-19. In human monocytes infected in vitro with SARS-CoV-2, the accumulation of LDs leads to the upregulation of lipid metabolism-related genes and the release of pro-inflammatory mediators such as leukotrienes (LTB4 and cysLT), chemokines (IL-8 and CXCL10), and inflammatory cytokines (IL-6, TNF, and IL-10). These inflammatory mediators amplify the immune response, leading to the recruitment and activation of immune cells at the site of infection and thereby contributing to COVID-19 development [68][69][104,105].
In fact, LDs are also sites of compartmentalized synthesis of eicosanoids during inflammatory conditions. Eicosanoids are inflammatory mediators that are derived from the breakdown of arachidonic acid (AA). Phospholipase A2 (PLA2) cleaves LDs and membrane phospholipids to produce AA. AA can be converted into prostaglandins (PGs), thromboxanes (TXs), or leukotrienes (LTs) by cyclooxygenases (COX) or lipoxygenases (LPX), which have regulatory roles in immunological homeostasis. PGE2, TXB2 and leukotriene B4 (LTB4) levels were higher in COVID-19 patients’ bronchoalveolar lavage fluid than in healthy controls. Also, eicosanoid levels were positively correlated with cytokines (IL-1, IL-6, TNF-, IL-12p70, IL-22, and IFN-2) and chemokines (CCL2, CCL11, CXCL9) [13][18]. PGE2, the most prevalent PG, is a key mediator in a variety of physiological processes, particularly the development and regulation of inflammation [70][106].
Leukotrienes are thought to be implicated in COVID-19 patients’ tissues because of increased neutrophil infiltration and neutrophil/lymphocyte ratios [71][108]. In addition, single-cell examination of COVID-19 patients’ bronchoalveolar immune cells and PBMCs reveals enhanced 5-lipoxygenase expression [72][73][109,110].
Furthermore, some viruses can employ LDs as a crucial site for viral component accumulation, assisting in the production of viral replication complexes [74][75][76][77][113,114,115,116]. It has been discovered that LDs can be used as platforms for the assembly and maturation of new virus particles just before release. SARS-CoV-2 proteins and ds-RNA are currently tightly connected with the LDs and, in some circumstances, colocalizing with LDs in an in vitro infection model, indicating a probable function for LDs in the SARS-CoV-2 replication cycle [12][17].
During COVID-19, the role of extracellular vesicles (EVs) in lipid metabolism remained limited. The transmission of viral components, including RNA, from infected to uninfected cells has been related to EVs. This could potentially facilitate the spread of the virus within the host, assisting viral replication and disease progression.
In parallel, there is evidence that cells can release LDs into the extracellular space, such as LDs being secreted from milk duct cells into milk [78][119] and LDs moving between epithelial cells in vitro (KB HeLa cells) [79][120]. It was also recently proposed that LDs could be bundled within adipocyte-derived EVs, activating macrophages in surrounding adipose tissue [80][121]. There is a strong synergy between these cellular particles based on their similarities and the increasing role of LDs in intercellular communication. Some data suggest a previously unknown overlap and potential interaction between EV and LDs [81][122].
