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Revealing the pulmonary surfactant corona on silica nanoparticles by cryo-transmission electron microscopy

Fanny Mousseau *a, Evdokia K. Oikonomou a, Annie Vacher b, Marc Airiau b, Stéphane Mornet c and Jean-François Berret a
aLaboratoire Matière et Systèmes Complexes, 10 Rue Alice Domon et Léonie Duquet, 75205 Paris Cedex, France. E-mail: fanny.mousseau@univ-paris-diderot.fr
bSolvay Research & Innovation Center Paris, 52 Rue de La Haie Coq, 93306 Aubervilliers Cedex, France
cInstitut de Chimie de La Matière Condensée de Bordeaux, UPR CNRS 9048, Université Bordeaux 1, 87 Avenue Du Docteur A. Schweitzer, Pessac Cedex F-33608, France

Received 13th December 2019 , Accepted 6th January 2020

First published on 7th January 2020


When inhaled, nanoparticles (NPs) deposit in alveoli and transit through the pulmonary surfactant (PS), a biofluid made of proteins and phospholipid vesicles. They form a corona reflecting the PS–nanomaterial interaction. Since the corona determines directly the NPs' biological fate, the question of its nature and structure is central. Here, we report on the corona architecture formed after incubation of positive or negative silica particles with Curosurf®, a biomimetic pulmonary surfactant of porcine origin. Using optical, electron and cryo-electron microscopy (cryo-TEM), we determine the pulmonary surfactant corona structure at different scales of observation. Contrary to common belief, the PS corona is not only constituted by phospholipid bilayers surrounding NPs but also by multiple hybrid structures derived from NP–vesicle interaction. Statistical analysis of cryo-TEM images provides interesting highlights about the nature of the corona depending on the particle charge. The influence of Curosurf® pre- or post-treatment is also investigated and demonstrates the need for protocol standardization.


Nanoparticles (NPs) in contact with biological fluids are rapidly covered by selected groups of biomolecules including proteins, lipids, specialized sugars, ions and enzymes, to form a corona that modifies nanomaterial interaction with cells and tissues.1,2 Following the work performed on protein corona in blood, research has started to address the problem of the corona formation in other biofluids, for instance the pulmonary surfactant (PS). When inhaled, nanoparticles may reach the alveolar space and come into contact with a thin layer (<1 μm) of the fluid lining the alveolar epithelium: the pulmonary surfactant.3 This fluid is made of phospholipids (90%) and proteins (10%) and its total concentration is estimated to be 40 g L−1.3 At the air–liquid interface, phospholipids are assembled into mono- and multi-layers while beneath the surface, they form multilamellar vesicles and tubular myelins.3 Upon contact with the PS, a corona of proteins and/or lipids is formed at the particle surface.4 Such a pulmonary surfactant corona (PS corona) is different from the one found with serum proteins in plasma.

The physicochemical characteristics of NPs, i.e. their chemical composition, size and surface charge, have been shown to notably affect NP interactions with lung fluids and to modify their cellular pathway, toxicity and uptake.5–7 Studying the PS corona for different nanomaterials is a major challenge in the fields of nanotoxicology and nanomedicine. Despite their importance in lung physiology, studies dealing with the PS corona are still scarce. They mainly rely on mass spectrometry results and on the determination of the corona chemical composition but provide little information about its structural organization.4,8–12 Recent studies focus on the modification of NP–cell interactions in the presence of the pulmonary surfactant.5,6,13–19 However, both mechanisms by which the PS corona is formed and its biological consequences remain open questions. Solving these issues requires in vitro and in vivo experiments under various conditions.

Pertaining to bioreactivity of nanomaterials in alveolar spaces, studies have shown that it is important to characterize their corona at the point of exposure. To this end, pioneering studies investigate the impact of hydroxyapatite and titanium oxide nanoparticles on the PS function and structure using transmission electron microscopy (TEM). NPs are shown to aggregate in solution or to be incorporated between PS bilayers, leading to a vesicular size reduction.20,21 However, the corona architecture could not be determined precisely because artefacts due to conventional staining or drying processes are generally present in TEM studies of assembled structures such as micelles or vesicles.22

The 2017 Nobel Prize in Chemistry was awarded to Jacques Dubochet, Richard Henderson, and Joachim Frank, for “developing cryo-electron microscopy for the high-resolution structure determination of biomolecules in solution”. Hence, cryo-TEM, the first reference method for the structural analysis of specific biological samples,22 was used for imaging the PS corona structure. Kumar et al. showed that silica or polymeric nanoparticles incubated in the PS lead to the spontaneous formation of a supported lipid bilayer (SLB)10 whereas Theodorou et al. demonstrated the formation of multilayers of phospholipids on silver and zinc oxide nanowires after bringing them in contact with the PS.18,23 Finally, Konduru et al. observed that cerium oxide and barium sulfate NPs incubated with the PS form hybrid NP–vesicle agglomerates.24 Thus the few available studies, which by the way display only zoomed images of some nanoparticles, lead to contradictory conclusions about the corona architecture. Concerning simulation, recent reports examine the spatial organization of lipid membranes with respect to the NPs. For instance, Hu et al. considered PS vesicles of complex lipid and protein compositions and showed that their interaction with silver or polystyrene NPs led to mono- or bilayer coating formation where proteins are also present.25

Here, we report the first statistical analysis of the pulmonary surfactant corona structure associated with nanoparticles. The NP/lipid assembly is investigated via optical microscopy, TEM and cryo-TEM for positive and negative silica particles, allowing us to draw the global picture of the PS corona. In addition, we study the impact of the formulation pathway on the corona structure (Materials and methods are detailed in ESI S1).

Curosurf® is the pulmonary surfactant considered in this work. This PS is extracted from minced pork lungs and is used for the surfactant replacement therapy of premature infants. Its lipid and protein compositions are provided in S1 and compared to those of the human surfactant. Fig. 1a displays the Curosurf® ultra-structure. As the human PS, it is composed of uni- and multi-lamellar vesicle ranging from dozens of nanometers to few microns. In our previous work, we provided extensive characterization of Curosurf® physico-chemical properties.26 In particular, we showed that Curosurf® vesicles exhibit a bimodal size distribution centered on 80 and 800 nm, have a zeta potential of −55 mV in MilliQ water and are made of 4.3 nm thick phospholipid bilayers present in the fluid state at 37 °C (S2). Amorphous silica particles have been selected due to their potential cytotoxicity when inhaled as dust.27,28 Indeed, silica inhalation can cause lung-related diseases including inflammation, silicosis and lung cancer. Positive and negative NPs of respectively 40 and 20 nm are used here to investigate the role of the nanoparticle charge in the PS corona structure. In the following, they are abbreviated as Silica (+) and Silica (−). In S1, the physico-chemical properties of these particles are summarized. In particular, their charge densities are determined to be +0.62 and −0.31 e nm−2 respectively.


image file: c9na00779b-f1.tif
Fig. 1 Cryo-TEM pictures of Curosurf® (a), Curosurf® and Silica (+) NPs (b) and Curosurf® and Silica (−) NPs (c). Additional images are provided in S4.

In a previous study, we demonstrated via Job scattering plots29 that the interaction of silica nanoparticles and Curosurf® is mainly driven by electrostatics.30 Here, we aim at disclosing the PS corona structure at the nano- and micrometer scales using a set of different techniques. First, optical microscopy is performed on Silica (+) or Silica (−) incubated with fluorescent Curosurf®31 (S3.1 and S3.2). The images show that pulmonary surfactant and Silica (+) interaction gives rise to large micrometer sized hybrid aggregates. Meanwhile, no such aggregates are found with Silica (−). TEM performed on Silica (+)/Curosurf® systems reveals that the aforementioned aggregates are of two kinds (Schemes 1 and S3.3). On the one hand, the particles act like stickers that bind the vesicles together via a physical link. On the other hand, hybrid aggregates contain pristine vesicles, bare particles and particles covered by a SLB. Our results suggest that the PS corona cannot be described only in terms of supported lipid bilayers and that a refined picture is necessary.


image file: c9na00779b-s1.tif
Scheme 1 Representation of the hybrid colloids present in the PS corona of positive and negative silica nanoparticles. The scales covered by the different techniques of microscopy used in this work are displayed in blue.

Cryo-TEM images in Fig. 1b–c and S4 show silica particles incubated with Curosurf®. Mixed silica-surfactant dispersions were prepared at concentrations inducing a surface ratio XS = 75, where XS denotes the ratio between the specific surface associated with the vesicles and that associated with the particles. Therefore, as under physiological conditions, the PS is present in large excess and is able to cover all the particles with a SLB. More than 800 NPs are analyzed for each particle type and classified depending on their assembly with phospholipids. Four different hybrid structures are found: NPs are either adsorbed at vesicles' outer membrane, internalized inside vesicles, aggregated with other particles or isolated (Scheme 1, arrows in Fig. 1 and Table 1, part a). As expected, significantly more particles are found internalized in vesicles than adsorbed at their outer surface irrespective of the NP charge. Indeed, particle internalization occurs if the adhesion energy between the particles and the membrane is greater than the bending energy associated with the wrapping process, e.g. above an estimated critical diameter of 20 nm.32 Given the dispersity of the two silica particles studied (Table S1.1), they are larger than this critical size. Moreover, statistics show that after incubation with Curosurf®, 63% of the positive NPs are internalized by vesicles whereas this number decreases to 43% for the negative particles (Table 1, part a). In addition, there are three times more Silica (−) isolated NPs than Silica (+) isolated ones. Close up views of these particles show that they are either bare or coated with a SLB (Fig. 1b-iv and c-iv). All these results are in agreement with our previous findings which indicated that Silica (+) interacts more strongly with Curosurf® than Silica (−) (S3). Table 1 shows that both positive and negative silica particles give similar hybrid structures in contact with the PS, but that the relative proportions of the different structures depend on the NP charge (note that a size effect cannot be completely excluded in the results obtained).

Table 1 Relative amount of sub-micron hybrid colloids present in the different PS coronas
image file: c9na00779b-u1.tif


Be that as it may, coupling cryo-TEM, TEM and optical microscopy enables us to retrieve a complete description of the PS corona (Scheme 1). NP–lipid interaction includes van der Waals and electrostatic interactions, hydration forces and bilayer thermal fluctuations.33 The mechanisms describing these interactions, and consequently the obtained hybrid structures, are thus complex and multifactorial. Hence, the coronas obtained in this work are specific to our experimental conditions, which highlights the general need to carefully characterize the corona formed for each NP/PS studied system.

Special attention is now drawn on internalized nanoparticles. While Silica (+) is found in uni- or multi-lamellar vesicles in equal numbers (45% versus 55%), 68% of Silica (−) are internalized in liposomes (Table 1, part b). Regardless of the particle charge and vesicle lamellarity, internalized particles exhibit a SLB34 (Fig. 1b-iii and c-iii). In the particular case of NPs inside multilamellar vesicles, particles are always found between the outer and inner membranes. This original engulfing process suggests that only the outer membrane initiates the internalization and confirms that SLB-coated NPs cannot enter liposomes.32

Each uni- and multi-lamellar vesicle containing particles is then analyzed based on 3 parameters: the number of internalized NPs, the vesicle lamellarity and the vesicle diameter. The results collected on more than 100 vesicles are summarized via 3D plots to establish cross-correlations between the aforementioned parameters. The patterns herein displayed are representative of the PS corona and differ one from another according to the NP charge (Fig. 2a–d). Then, the lamellarity and the vesicle diameter versus the number of internalized particles are plotted (Fig. 2e and f). The results show that up to 23 nanoparticles can be wrapped by vesicles and that on average, this value is not affected by the particle charge. Interestingly, the diameter of vesicles containing NPs varies linearly with the amount of captured NPs, with a slope 3 times higher for the Silica (+). Thus, as vesicles become larger, their lamellarity increases and they are able to invaginate more positive NPs. In contrast, Silica (−) is mainly internalized by liposomes, as shown in Table 1, part b. Our results are in agreement with those of Konduru et al. where positive cerium oxide NPs interact mainly with multilamellar vesicles of the PS whereas negative barium sulfate NPs interact with liposomes in majority.24 Definitely, our study shows that the PS corona structure is significantly different when formed on positive or negative silica nanoparticles. This outcome is of major importance since the binding of the PS to a variety of nanoparticles has been shown to influence their cellular uptake, intracellular localization, oxidative properties, inflammation potential and their toxicity in the lungs.14,16,18,19


image file: c9na00779b-f2.tif
Fig. 2 (a–d) 3D plot representation of the number of internalized NPs as a function of the vesicle lamellarity and diameter. The bubble size is proportional to the number of wrapped NPs (a and c) or to the lamellarity of the vesicles (b and d). (e and f) Mean diameter and mean lamellarity of vesicles as a function of the number of internalized NPs for positive (dark circles) and negative (bright circles) NPs. In (f), lines are a guide for the eye.

Finally, the influence of the formulation pathway on the PS corona structure is studied for two reasons. First, liposomes made of synthetic phospholipids and obtained by extrusion are often used as a PS substitute in physico-chemical studies on NPs/PS interactions. Second, in in vitro cellular assays NPs are usually incubated in the PS and then sonicated to allow their dispersion before being brought into contact with cells.24,35 In the following, we thus investigate how pre-extrusion of the PS and post-sonication of NP/PS systems affect the corona structure. With this aim, Silica (+) particles are incubated with extruded Curosurf® (vesicle diameter reduced from 800 nm to 130 nm, S5). Cryo-TEM images show that 90% of the NPs are comprised in large micron-sized aggregates (Table 1 and Fig. 3a) and that the hybrid assemblies are indeed made of bare and SLB-coated particles (Fig. 3a-ii). As the latter are negative,19 aggregation probably results from electrostatic interaction of oppositely charged species. In a second assay, Silica (+) and Curosurf® are incubated and then sonicated. 100% of particles are found to be non-aggregated and coated with a SLB (Fig. 3b) as observed on other systems.36,37 Our results demonstrate that pre- or post-treatment of Curosurf® such as extrusion and sonication strongly modifies the PS corona.


image file: c9na00779b-f3.tif
Fig. 3 Cryo-TEM images of Silica (+)/Curosurf ® systems with extruded Curosurf® (a) or after sonication (b). In (a-ii), orange and blue arrows indicate respectively naked and coated NPs.

Conclusions

For the first time to our knowledge, the PS corona structure was investigated with cryo-TEM over more than 2400 NPs, allowing a statistical analysis. Our results show for the first time that the corona is not limited to supported lipid bilayers, as sometimes assumed in the literature, but comprises a wide variety of intermediate structures. We thus provide a new definition of the PS corona: the pulmonary surfactant corona is the pattern constituted by the different hybrid structures formed by NPs and phospholipids and by their relative amounts. Second, we demonstrate that membrane and particle electrostatic charges control the interaction, and consequently the PS corona. These findings have significant implications in pulmonary toxicity studies on nanoparticles, and our results have to be validated in animals now. In addition, pre- or post-pulmonary surfactant treatment is shown to significantly affect the PS corona, which underlines the need for sample preparation protocol harmonization to avoid the physico-chemical or biological studies of unrelevant coronas.

Understanding the PS corona is crucial. First, the formation of this corona may interfere with the physiological function of the endogenous PS. Second, because the PS corona is formed at the initial biological barrier in the lungs, its biophysicochemical properties determine the subsequent biological identity and fate of the inhaled NPs. Thus, knowing the PS corona architecture will shed light on understanding the molecular mechanism of nano-bio interactions in the respiratory system. Third, understanding the PS corona structure and formation is a way to intentionally formulate specific NP/PS colloids effective as drug delivery carriers in lungs.36

Conflicts of interest

There are no conflicts to declare.

Acknowledgements

ANR (Agence Nationale de la Recherche) and Solvay are gratefully acknowledged for their financial support of this work through ANR-12-CHEX-0011 (PULMONANO).

Notes and references

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Footnote

Electronic supplementary information (ESI) available. See DOI: 10.1039/c9na00779b

This journal is © The Royal Society of Chemistry 2020