- Open Access
Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
Malaria Journal volume 13, Article number: 230 (2014)
The mechanisms through which infection with Plasmodium spp. result in lung disease are largely unknown. Recently a number of mouse models have been developed to research malaria-associated lung injury but no detailed ultrastructure studies of the disease in its terminal stages in a murine model have yet been published. The goal was to perform an ultrastructural analysis of the lungs of mice that died with malaria-associated acute lung injury/acute respiratory distress syndrome to better determine the relevancy of the murine models and investigate the mechanism of disease.
DBA/2 mice were infected with Plasmodium berghei strain ANKA. Mice had their lungs removed immediately after death, processed using standard methods and viewed by transmission electron microscopy (TEM).
Infected red blood cell:endothelium contact, swollen endothelium with distended cytoplasmic extensions and thickening of endothelium basement membrane were observed. Septa were thick and filled with congested capillaries and leukocytes and the alveolar spaces contained blood cells, oedema and cell debris.
Results show that the lung ultrastructure of P. berghei ANKA-infected mice has similar features to what has been described in post-mortem TEM studies of lungs from individuals infected with Plasmodium falciparum. These data support the use of murine models to study malaria-associated acute lung injury.
Malaria-associated acute lung injury/acute respiratory distress syndrome (malaria associated ALI/ARDS) is a manifestation of severe malaria which can result from infection with a number of Plasmodium spp. including Plasmodium falciparum, Plasmodium vivax and Plasmodium knowlesi (reviewed in ). It has a high mortality rate , however how and why malaria-associated ALI/ARDS occurs is largely unknown.
Gas exchange in the lungs occurs in the alveoli that are separated by septa in which there is a network of capillaries as well as collagen, muscle cells, leukocytes and other interstitial cells. Gases in the alveoli need to traffic to the blood in the capillaries, through the alveoli epithelial cells and the capillaries’ endothelium. Lung injury generally involves inflammation which can cause damage to the alveolar epithelial and/or capillary endothelial cells causing hypoxemia . Morphological studies can help our understanding of lung disease and malaria and, though light microscopy can provide considerable information, it is limited when it comes to the exploration of fine-structural abnormalities. Ultrastructural analysis by electron microscopy has the potential to provide valuable information about the pathology of malaria-associated ALI/ARDS. Currently there are only a few papers describing lung ultrastructure in malaria [3–5]. These papers, looking at lung injury caused by P. falciparum in humans, describe infected red blood cells (iRBCs) in close contact with the endothelium of alveolar capillaries, interstitial oedema and thickening of the septa as well as swelling of the endothelial cells resulting in a narrowing of the capillaries. The capillaries are described as occluded by iRBCs [3, 4], non-infected red blood cell (niRBCs), monocytes [3–5], and neutrophils and lymphocytes . Leukocytes are visible in the septa  and fibrin in the septa is described as absent, focal or widespread . Taken together these results suggest there might be a role for iRBC: endothelial binding in lung injury, and that the narrowing of the capillaries, oedema and presence of leukocytes are likely the morphological basis for respiratory distress [3, 4].
Recently a number of murine models have been published with a focus on the lung and malaria [6–9] and, to date, models have been able to provide evidence that a number of factors, including vascular endothelial growth factor , neutrophils , platelets , haemozoin , CD36 dependent iRBC sequestration , and sodium transporter activity  play a role in disease. Lungs from mice which die of acute lung injury can have very different lung pathologies compared to other murine models such as cerebral malaria seen with C57BL/6 infected with Plasmodium berghei strain ANKA, including increased oedema and haemorrhages in the lung . However, although the use of murine models to examine malaria-associated ALI/ARDS is a growing area of research there are no ultrastructural descriptions available for the terminal stage of the disease in a murine model.
In mice, only one short description of electron microscopy observations of the lung in malaria has been published . That study describes the pathology seen early in infection (zero to five days) in P. berghei- and Plasmodium yoelii-infected mice (the mouse strain was not specified). Observations included aggregation of platelets in the capillaries at day 2, enlarged neutrophils in capillaries, distended cytoplasmic extensions of endothelial cells and alveolar macrophages in the alveolar space at day 4 and swollen endothelial cells with cytoplasmic sheets together with neutrophils occupying the capillary space at day 5 post infection .
In this study, the aim was to perform a detailed ultrastructural analysis of the lungs of mice that died with malaria-associated ALI/ARDS. It is hoped that this analysis will aid the comparison of the mouse model with human malaria-associated lung injury in order to better determine the relevancy of murine models when researching lung injury and allow the investigation of the morphological basis of the disease. This study describes the ultrastructure of the lungs of mice that have died with malaria-associated ALI/ARDS using the model of DBA/2 mice infected with P. berghei strain ANKA (clone 1.49L) .
Animals and infection
Six- to eight-week-old male DBA/2 mice were bred under pathogen-free conditions in isogenic mouse facilities in Department of Parasitology, University of São Paulo, Brazil. The mice were housed five animals per cage in standard polycarbonate cages on wood-shaving bedding. They were fed ad libitum and had unrestricted access to water. They were kept under controlled temperature and humidity in a light and dark cycle of 12 hrs each. Mice were intraperitoneally infected with 1×106P. berghei ANKA (clone 1.49L) iRBCs, as previously described . All protocols were approved by the Health Committee of the Biomedical Sciences Institute of the University of São Paulo (CEUA n°003 page 98 book2 and CEUA n°054 page 128 book2) established by the Brazilian College of Animal Experimentation (COBEA).
Transmission electron microscopy
For transmission electron microscopy (TEM) lung tissue was obtained immediately after death from two non-infected (NI) and three ALI/ARDS mice (in ALI/ARDS mice this was at nine days post infection), cut into small pieces (1 mm3) and fixed by immersion in 2% glutaraldehyde at 4°C, rinsed in 0.1 M phosphate buffer (pH 7.4), followed by post fixation in 1% osmium tetroxide, and block staining in 1% aqueous uranyl acetate, dehydrated using alcohol. The tissues were embedded in 100 EPON for 48 hrs at 70°C. Ultra-thin sections of 70 nm were cut and stained 2% uranil acetate and lead citrate, and examined under a Jeol JEM 1010 transmission electron microscope.
Lung tissue was obtained immediately after death (in infected mice this was between seven to 12 days post infection), fixed in formalin (10%) for 24-48 hrs then placed in ethanol until put in paraffin, sectioned (5 μm) and stained with haematoxylin and eosin (HE), Masson’s Trichrome Stain or Picrosirius Red. Quantitative comparison of thickness of alveolar septa of ALI/ARDS and control lungs was done on slides from five NI and five ALI/ARDS lungs by overlaying a 20 um2 grid on a 40-fold objective image of HE-stained tissue and measuring septa width where the grid crossed the tissue in the thinnest direction (50 measurements/image and three images/mouse lung). Masson’s Trichrome-stained slides six NI and five ALI/ARDS lungs were examined under a 20-fold objective for fibrotic changes in the septa. Degrees of fibrosis were from Grade 0, no fibrotic changes and Grade 1 isolated alveolar septa with gentle fibrotic changes to Grade 8 fibrous obliteration as defined by Hubner et al.. Observations were confirmed in consecutive Picrosirius Red tissue sections of select mice.
DBA/2 mice infected with P. berghei ANKA that died of ALI died between seven to 12 days post infection (Figure 1A). An observation of the gross pathology of the lungs revealed pleural effusion and red swollen lungs. Parasitaemia of mice that died of lung injury during this period was typically on average 20% (Figure 1B). HE and TEM images showed that the morphology of ALI/ARDS lungs were completely different when compared with lungs from non-infected mice, with ALI/ARDS lungs showing oedema, haemorrhage and thickened septa filled with congested capillaries, iRBCs and leukocytes (Figure 2).
TEM of ALI/ARDS lungs showed iRBCs in close contact with the endothelium. This close contact was seen in both non-congested (Figure 3A) and congested capillaries (Figure 3D). In some fields, bridges between the iRBCs and the endothelium were observed (Figure 3B, C, E and F). Congested capillaries seen by light microscopy in HE-stained ALI/ARDS lungs (Figure 4B) were filled with iRBCs, niRBCs and leukocytes (Figure 4B, insert); these observations were confirmed by TEM (Figure 2D, C and D). Some of the congested capillaries showed swollen endothelial cells (Figure 4C and D) and/or thickened endothelial (but not epithelial) basement membrane (Figure 5B). The swollen endothelium included distended cytoplasmic extensions cutting across the alveolar space (Figure 4D). In one field, fenestrated endothelium was observed (Figure 5).
Quantitative examination of HE-stained lungs showed septa of ALI/ARDS lungs were 80% thicker (6.5 μm ± 0.4 μm) compared to septa of the non-infected controls (3.6 μm ± 0.4 μm) (Figure 6). The thickened septa were not associated with fibrosis as examination of ALI/ARDS lungs and non-infected control lungs stained with Masson’s Trichrome (Figure 7A and D) showed Grade 0 fibrosis (no fibrosis). Additionally, examination of Picrosirius Red-stained ALI/ARDS lungs also showed no fibrosis (Figure 7B and E). Also TEM images of ALI/ARDS and non-infected control lungs showed only small isolated areas with collagen (Figure 7C and F) and there was no obvious proliferation of fibroblasts. Instead TEM images revealed that the septa of ALI/ARDS mice were thickened with a marked leukocyte infiltrate (Figures 2D and 6D), which included macrophages and neutrophils (Figures 6D and 8B). A number of these cells in the septa, such as macrophages, appeared to have phagocytozed erythrocytes (both iRBC and niRBC). Some inflammatory cells in the septa also appeared to have swollen mitochondria (Figure 8C). In many fields the epithelium appeared to have marked projections into the alveolar space (Figure 8A). Neither epithelial apoptosis nor proliferation of epithelial cells was observed.
The alveolar space of ALI/ARDS lungs was filled with oedema (Figure 2D) and also contained cells and cellular debris. These were identified by TEM as iRBCs (Figure 9A), degraded surfactant (Figure 9B) and leukocytes (Figure 9A and D), including alveolar macrophages (Figure 9C). The alveolar macrophage contained crystals, possibly haemozoin (Figure 9C).
This study represents the first description of the lung ultrastructure of mice that have died with malaria-associated ALI/ARDS.
Although ALI/ARDS can be caused by exposure of either the alveoli or the capillaries to a large variety of harmful agents, its progression generally follows certain patterns . Damage in the capillaries is often first seen with sub-endothelial and endothelial oedema, followed by necrosis of endothelial cells, which results in nude basement membrane. More serious injuries often involve the presence of high numbers of inflammatory cells in the septa and damage to the epithelium (primarily epithelium type I), which results in alveolar oedema (often along with hyaline membrane formation). Extensive and prolonged injury or severe epithelial damage is also often associated with stimulation of fibroblasts and collagen deposition (reviewed in ).
This study, looking at malaria-associated ALI/ARDS, showed a number of these characteristics. TEM images of infected lungs showed damage to the endothelium, namely endothelial swelling with distended cytoplasmic extensions and thickening of the endothelial basement membrane. The presence of oedema, blood and debris in the alveolar spaces was observed. Although, as in other TEM studies of malaria-associated lung injury, injured epithelium by TEM was not seen [3, 4], it must be remembered that this method only looks at a small section of tissue and so it cannot be concluded that epithelial damage is completely absent. Also the presence of oedema seen in the murine model and in post mortem cases of malaria-associated lung injury (reviewed in ), as well as red blood cells in the alveolar space suggests breakdown of barriers and that epithelial damage is occurring. It is possible that epithelium damage occurs in isolated areas and/or that the oedema is at least partly due to reduced activity of epithelium sodium channels  (as opposed to a physical breakdown of the barrier).
Capillary congestion was one of the most prominent observations by both light microscopy and TEM. It is likely that this congestion results in inefficient blood flow and blood gas exchange in the lungs and TEM images provide evidence as to which factors may be contributing to it. When observing iRBCs in close contact with endothelial cells, and in some fields, bridges were seen between the endothelium and iRBCs. This provides evidence that iRBC:endothelium adherence is occurring in the mouse lung, possibly resulting in the accumulation of parasites in the lungs. This observation complements studies which suggest that CD36-dependent iRBC sequestration is related to disease severity by contributing to parasite levels in the lung  and murine malaria-associated lung injury . Sequestration may also contribute to pathology by preventing parasite removal by the spleen, promoting parasite growth  and activating endothelial cells .
In addition to iRBC:endothelium binding, another factor that may contribute to capillary congestion is the endothelium swelling, especially with the endothelium extensions cutting through the capillary lumen. It is hypothesized that the swelling and extensions are an indication of activated endothelium and/or microthrombi organization. In vitro studies could provide more information regarding the role of iRBC:endothelium interactions.
The presence of various leukocytes in the lung’s capillaries, septa and alveolar spaces suggests that inflammation plays an important part in the pathogenesis of malaria-associated lung injury in this model. Monocyte/macrophages and neutrophils have been identified previously by electron microscopy in both human [3–5, 20] and murine [10, 13] malaria-associated lung injury. Monocytes/macrophages are consistently observed in human studies and often contain haemozoin indicating phagocytosis of infected cells [1, 3, 4, 21], and their presence could result in the production of pro-inflammatory products that could also contribute to endothelial injury . The observation of an alveolar macrophage with vesicles filled with crystals (likely haemozoin) suggests that alveolar macrophages play a role in clearing parasites from the alveolar space. Neutrophils have been highlighted as playing a role in severe disease caused by P. berghei ANKA, possibly by contributing to pulmonary lesions . In humans however, the role of neutrophils in lung injury during P. falciparum malaria still needs to be clarified, as ultrastructural studies of human lungs in severe malaria noted the presence of monocytes [3, 4, 20] and only one study noted the presence of neutrophils . As lung injury due to other causes is often associated with high numbers of neutrophils in the lungs, the role of neutrophils in Plasmodium-induced lung injury in humans should be a research priority in order to clarify whether the mechanisms of disease in non-malaria associated ALI/ARDS can be extrapolated to those of malaria-associated ALI/ARDS.
In humans, lung fibrosis occurs in some but not all individuals suffering from malaria-associated lung injury ; no evidence of fibrosis was observed suggesting that this murine model is not suited for investigating the role of fibrosis (if there is any) in malaria-associated lung injury. This may be due to the fact that the mice die before 12 days post infection and instead, mouse models of severe disease that rely on a longer time-frame of infection may be more suitable for looking at fibrosis. Curiously, a fenestrated endothelial cell was observed by TEM, possibly indicating the very beginning of fibrosis in the lungs , however it is best not to over-interpret this.
This is the first detailed ultrastructural analysis of lungs of mice that have died with malaria-associated ALI/ARDS. These results show that iRBC:endothelium binding and endothelium swelling with cytoplasmic extensions are present and likely contribute to the occlusion of the capillaries. Damage to the endothelium was clear with the swelling and thickening of the endothelium basement membrane. In contrast, damage to the epithelium was less obvious and it was not possible to confirm if the alveolar oedema that was observed was due to damage of the epithelial layer. Thickening of septa occurred and was attributed to extensive leukocyte infiltrate, occluded capillaries and cellular oedema, while there seemed not to exist any significant fibrosis. The excessive numbers of leukocytes in the capillaries and septa highlight the role of inflammation in lung injury. A summary of the changes seen by electron microscopy is represented in diagram in Figure 10.
It is shown here for the first time that the lung ultrastructure in mice that died with malaria-associated ALI/ARDS, after infection with P. berghei ANKA, has many similar features to what has been described in post-mortem TEM studies of lungs from individuals infected with P. falciparum. Some of these similarities are the presence of inflammatory cells, oedema, occluded capillaries, swollen endothelium, and iRBC:endothelium contact. Although human malaria-associated lung injury still needs to be further investigated in order to clarify some morphological characteristics of the disease, overall these data support the use of murine models to study malaria-associated lung injury.
Acute lung injury
Acute respiratory distress syndrome
Haematoxylin and eosin
Infected red blood cell
Non-infected red blood cell
Transmission electron microscopy.
Taylor WRJ, Hanson J, Turner GDH, White NJ, Dondorp AM: Respiratory manifestations of malaria. Chest. 2012, 142: 492-505. 10.1378/chest.11-2655.
Thompson BT, Moss M: A new definition for the acute respiratory distress syndrome. Semin Respir Crit Care Med. 2013, 34: 441-447. 10.1055/s-0033-1351162.
Duarte MI, Corbett CE, Boulos M, Amato Neto V: Ultrastructure of the lung in falciparum malaria. Am J Trop Med Hyg. 1985, 34: 31-35.
Corbett CE, Duarte MI, Lancellotti CL, Silva MA, Andrade Júnior HF: Cytoadherence in human falciparum malaria as a cause of respiratory distress. J Trop Med Hyg. 1989, 92: 112-120.
Mackenzie C, Carr R, Das A, Lucas S, Liomba N, Grau G, Molyneux M, Taylor T: Electron microscopy of the lung in fatal pediatric cerebral malaria. Am J Trop Med Hyg. 1999, 61 (Supplement 1): 269-
Epiphanio S, Campos MG, Pamplona A, Carapau D, Pena AC, Ataíde R, Monteiro CAA, Félix N, Costa Silva A, Marinho CRF, Dias S, Mota MM: VEGF promotes malaria-associated acute lung injury in mice. PLoS Pathog. 2010, 6: e1000916-10.1371/journal.ppat.1000916.
Hee L, Dinudom A, Mitchell AJ, Grau GE, Cook DI, Hunt NH, Ball HJ: Reduced activity of the epithelial sodium channel in malaria-induced pulmonary oedema in mice. Int J Parasitol. 2011, 41: 81-88. 10.1016/j.ijpara.2010.07.013.
Van den Steen PE, Geurts N, Deroost K, Van Aelst I, Verhenne S, Heremans H, Van Damme J, Opdenakker G: Immunopathology and dexamethasone therapy in a new model for malaria-associated acute respiratory distress syndrome. Am J Respir Crit Care Med. 2010, 181: 957-968. 10.1164/rccm.200905-0786OC.
Lovegrove FE, Gharib SA, Peña Castillo L, Patel SN, Ruzinski JT, Hughes TR, Liles WC, Kain KC: Parasite burden and CD36-mediated sequestration are determinants of acute lung injury in an experimental malaria model. PLoS Pathog. 2008, 4: e1000068-10.1371/journal.ppat.1000068.
Senaldi G, Vesin C, Chang R, Grau GE, Piguet PF: Role of polymorphonuclear neutrophil leukocytes and their integrin CD11a (LFA-1) in the pathogenesis of severe murine malaria. Infect Immun. 1994, 62: 1144-1149.
Lacerda Queiroz N, Rachid MA, Teixeira MM, Teixeira AL: The role of platelet-activating factor receptor (PAFR) in lung pathology during experimental malaria. Int J Parasitol. 2013, 43: 11-15. 10.1016/j.ijpara.2012.11.008.
Deroost K, Tyberghein A, Lays N, Noppen S, Schwarzer E, Vanstreels E, Komuta M, Prato M, Lin J-W, Pamplona A, Janse CJ, Arese P, Roskams T, Daelemans D, Opdenakker G, Van den Steen PE: Hemozoin induces lung inflammation and correlates with malaria-associated acute respiratory distress syndrome. Am J Respir Cell Mol Biol. 2013, 48: 589-600. 10.1165/rcmb.2012-0450OC.
Suzuki S: Lung events in mice infected with rodent plasmodia. Trans R Soc Trop Med Hyg. 1975, 69: 20-
Hübner RH, Gitter W, El Mokhtari NE, Mathiak M, Both M, Bolte H, Freitag Wolf S, Bewig B: Standardized quantification of pulmonary fibrosis in histological samples. Biotechniques. 2008, 44: 507-511. 10.2144/000112729. 514–517
Adamson IYR: Alveolar Injury and Repair. Electron Microscopy of the Lung. Volume 48. Edited by: Schraufnagel D, Dekker SD. 1990, New York: Marcel Dekker; Lenfant C (Series Editor): Lung Biology in Health and disease, 165-172.
VanDen Steen PE, Deroost K, Deckers J, Van Herck E, Struyf S, Opdenakker G: Pathogenesis of malaria-associated acute respiratory distress syndrome. Trends Parasitol. 2013, 29: 346-358. 10.1016/j.pt.2013.04.006.
Franke Fayard B, Trueman H, Ramesar J, Mendoza J, Keur M, Van Der Linden R, Van Der Sinden RE, Waters AP, Janse CJ: A Plasmodium berghei reference line that constitutively expresses GFP at a high level throughout the complete life cycle. Mol Biochem Parasitol. 2004, 137: 23-33. 10.1016/j.molbiopara.2004.04.007.
Fonager J, Pasini EM, Braks JAM, Klop O, Ramesar J, Remarque EJ, Vroegrijk IOCM, van Duinen SG, Thomas AW, Khan SM, Mann M, Kocken CHM, Janse CJ, Franke-Fayard BMD: Reduced CD36-dependent tissue sequestration of Plasmodium-infected erythrocytes is detrimental to malaria parasite growth in vivo. J Exp Med. 2012, 209: 93-107. 10.1084/jem.20110762.
Viebig NK, Wulbrand U, Förster R, Andrews KT, Lanzer M, Knolle PA: Direct activation of human endothelial cells by Plasmodium falciparum-infected erythrocytes. Infect Immun. 2005, 73: 3271-3277. 10.1128/IAI.73.6.3271-3277.2005.
MacPherson GG, Warrell MJ, White NJ, Looareesuwan S, Warrell DA: Human cerebral malaria. A quantitative ultrastructural analysis of parasitized erythrocyte sequestration. Am J Pathol. 1985, 119: 385-401.
Punyagupta S, Srichaikul T, Nitiyanant P, Petchclai B: Acute pulmonary insufficiency in falciparum malaria: summary of 12 cases with evidence of disseminated intravascular coagulation. Am J Trop Med Hyg. 1974, 23: 551-559.
Chua CLL, Brown G, Hamilton JA, Rogerson S, Boeuf P: Monocytes and macrophages in malaria: protection or pathology?. Trends Parasitol. 2013, 29: 26-34. 10.1016/j.pt.2012.10.002.
Carr R, Lucas S, Liomba N, Whitten R, Grau G, Mackenzie C, Molyneux M, Taylor T, Das A: Lung pathology in fatal pediatric malaria. Am J Trop Med Hyg. 1999, 61 (Supplement 1): 260-270.
Kawanami O, Matsuda K, Yoneyama H, Ferrans VJ, Crystal RG: Endothelial fenestration of the alveolar capillaries in interstitial fibrotic lung diseases. Acta Pathol Jpn. 1992, 42: 177-184.
Baron R, Perrella M: Pathogenesis of Acute Lung Injury: Experimental Studies. Acute Respiratory Distress Syndrome, Volume 233. Edited by: Choi AMK. 2010, New York: Informa Healthcare; Lenfant C (Series Editor): Lung Biology in Health and disease, 59-71.
Diep BA, Chan L, Tattevin P, Kajikawa O, Martin TR, Basuino L, Mai TT, Marbach H, Braughton KR, Whitney AR, Gardner DJ, Fan X, Tseng CW, Liu GY, Badiou C, Etienne J, Lina G, Matthay MA, DeLeo FR, Chambers HF: Polymorphonuclear leukocytes mediate Staphylococcus aureus Panton-Valentine leukocidin-induced lung inflammation and injury. Proc Natl Acad Sci U S A. 2010, 107: 5587-5592. 10.1073/pnas.0912403107.
Fauci A, Kasper D, Braunwald E, Hauser S, Londo D, Jameson J, Loscalzo J: Acute Respiratory Distress Syndrome. Harrison’s Princ Intern Med. 2008, New York: Mcgraw-hill, 17
We thank Bernardo Paulo Albe for technical support.
Financial support was provided by grants 2009/53256-7 (SE) and 2009/53889-0 (CRFM) from the São Paulo Research Foundation (FAPESP) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 306668/2012-2. EHA was supported by a FAPESP fellowship (2011/195252-0).
The authors declare no commercial or other associations that might pose competing interests.
EHA designed and performed the experiments, discussed the results, analysed the data and wrote the manuscript. RB, SE and EMN designed and performed the experiments, discussed the results and analysed the data. JMA, CRFM, EGC, and SE conceived and designed the study, discussed the results and wrote the manuscript. MRIL reviewed the manuscript. CRFM and SE funded this work. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Aitken, E.H., Negri, E.M., Barboza, R. et al. Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome. Malar J 13, 230 (2014). https://doi.org/10.1186/1475-2875-13-230
- Acute lung injury (ALI)
- Acute respiratory distress syndrome (ARDS)
- Transmission electron microscopy
- Murine model