Elemental analysis of lung tissue particles and intracellular iron content of alveolar macrophages in pulmonary alveolar proteinosis
© Shimizu et al; licensee BioMed Central Ltd. 2011
Received: 31 March 2011
Accepted: 30 June 2011
Published: 1 December 2011
Pulmonary alveolar proteinosis (PAP) is a rare disease occurred by idiopathic (autoimmune) or secondary to particle inhalation. The in-air microparticle induced X-ray emission (in-air micro-PIXE) system performs elemental analysis of materials by irradiation with a proton microbeam, and allows visualization of the spatial distribution and quantitation of various elements with very low background noise. The aim of this study was to assess the secondary PAP due to inhalation of harmful particles by employing in-air micro-PIXE analysis for particles and intracellular iron in parafin-embedded lung tissue specimens obtained from a PAP patient comparing with normal lung tissue from a non-PAP patient. The iron inside alveolar macrophages was stained with Berlin blue, and its distribution was compared with that on micro-PIXE images.
The elements composing particles and their locations in the PAP specimens could be identified by in-air micro-PIXE analysis, with magnesium (Mg), aluminum (Al), silicon (Si), phosphorus (P), sulfur (S), scandium (Sc), potassium (K), calcium (Ca), titanium (Ti), chromium (Cr), copper (Cu), manganase (Mn), iron (Fe), and zinc (Zn) being detected. Si was the major component of the particles. Serial sections stained by Berlin blue revealed accumulation of sideromacrophages that had phagocytosed the particles. The intracellular iron content of alveolar macrophage from the surfactant-rich area in PAP was higher than normal lung tissue in control lung by both in-air micro-PIXE analysis and Berlin blue staining.
The present study demonstrated the efficacy of in-air micro-PIXE for analyzing the distribution and composition of lung particles. The intracellular iron content of single cells was determined by simultaneous two-dimensional and elemental analysis of paraffin-embedded lung tissue sections. The results suggest that secondary PAP is associated with exposure to inhaled particles and accumulation of iron in alveolar macrophages.
Pulmonary alveolar proteinosis is a rare disease characterized by dense accumulation of surfactant and phospholipids in the alveoli and distal airways . Progression of this disease leads to respiratory failure . Auto anti-granulocyte-macrophage colony-stimulating factor (anti-GM-CSF) antibody is involved in the development of the idiopathic (autoimmune) form of PAP . PAP may also associate with malignancies and secondary to particle exposures [4–8]. Considering the latter, a recent report from Japan revealed exposure to dust in 23% of 223 cases of PAP . Thus, particles are considered to be one of the causative agents of secondary PAP. Disturbance of iron (Fe) homeostasis has been reported in idiopathic PAP patients. Present knowledge provides little information about the mechanisms behind the observed accumulation of iron in lung tissues and alveolar macrophages. However, in cases of secondary PAP, Fe bound to the inhaled particles may be a potential source of iron [10, 11]. Also, Fe-catalyzed oxidant-induced rupture of lysosomes and consequent apoptosis of alveolar macrophages has been proposed to be involved in idiopathic PAP. To follow disease progression, routine examination for haemosiderin (Fe) in the macrophages of idiopathic PAP patients has been proposed .
The aim of this study was to assess the secondary PAP due to inhalation of harmful particles by employing in-air microparticle induced X-ray emission (in-air micro-PIXE) analysis for particles and intracellular iron in lung tissue specimens combined with Berlin blue staining for iron.
Patient and sample preparation
PAP lung tissue was obtained from a 64-year-old woman at video-assisted thoracoscopic surgery (VATS). She was a hairdresser, and a current smoker (10 pack-years). Serum anti-GM-CSF antibody was negative analysis. Pathological examination revealed interstitial pneumonia with interstitial fibrosis and periodic acid-Schiff (PAS)-positive material in the alveolar spaces. The pathological diagnosis was pulmonary alveolar proteinosis. As a control, normal lung tissue was obtained from a 72-years-old woman with lung cancer of adenocarcinoma. She was a housewife, and a never smoker without history of occupational exposure of particles. She received a lobectomy at surgical resection, and the normal lung of the margin of tumor was used for the analysis. Tissues were subjected to in-air micro-PIXE analysis and Berlin blue staining for iron.
In-air micro-PIXE analysis
In-air micro-PIXE analysis of dense particles area in PAP tissue
In-air micro-PIXE analysis of alveolar macrophages in surfactant-rich area
Quantitative analysis for iron in tissue section
The Fe/P ratios calculated by in-air PIXE analysis were 0.28, 0.36 and 0.0036 for a dense particles phagocytosed by macrophages in PAP, an alveolar macrophage in surfactant-rich area of PAP and an alveolar macrophage of control, respectively.
Disturbance of iron homeostasis has been reported in PAP , and alveolar macrophages from BAL have a high Fe content . In that study, the cellular distribution of iron was evaluated by Berlin blue staining, and measurement of the cellular Fe content was done by atomic absorption spectrometry after lysis of the cells. In the present study, there are two morphologic characteristics of this PAP-case needed to study, the first in the lung tissue cells (mainly siderophages) with dense particles containing large amounts of Si and Fe, and the second in alveolar macrophages in the alveoli containing large amounts of iron in intracellulary digesting deposits of surfactant. In-air micro-PIXE system was used to assess the distribution of intracellular Fe in macrophages. The Fe/P ratio has been used for evaluation of iron overload to the cells . Present study revealed that the Fe/P ratio in a single macrophage in PAP was very high compared to control lung. Silica particles were detected in control lung. Silica deposition is frequently observed in normal lung without history of occupational exposure . In control lung, it seemed that silica particles did not increase intracellular iron of macrophages by analysis of in-air micro PIXE and Berlin blue staining. Elemental analysis showed the Kβ peak of Fe appeared separately from Kα peak, and near the peak of cobalt (Co). The Kα peak appears when an electron transits from L to K electron shell by irradiation for sample, and the Kβ peak appears when an electron transits from M to K electron shell by irradiation for sample. In our micro-PIXE system, the peaks of Kα and Kβ for light element appear close to each other because of nearly energy levels. However, the peaks of Kα and Kβ for heavy elements, in present case Fe, appear separately. In present case, the calculation of Fe/P ratio was performed using the formula taking account Kα for heavy elements, as previously [12, 16].
Cases of PAP had been reported in association with occupational and environmental exposure to substances such as indium oxide, indium-tin oxide, silica, titanium, aluminum, cotton, and fibrous material [4–8]. A recent study from Japan showed that exposure to dust was associated with PAP . In the present study, in-air-micro-PIXE analysis revealed the existence of particles with a high Si contents with Fe in lung tissue from a PAP patient. There has already been a report about a PAP patient who was a hairdresser , but the association between particles and the materials used by hairdressers could not be assessed in present case. Although the association of cigarette smoking and PAP has not been determined , tobacco smoke could not be excluded as the source of the iron. However, it is necessary to examine lung particles derived from smoking by in-air micro-PIXE in a setting with few environmental factors such as an animal model.
As a factor in the onset of PAP, iron-induced oxidative stress and lysosomal rupture following the disturbance of iron homeostasis may play a role [10, 11]. In this study, the Fe/P ratio was measured in an alveolar macrophage from PAP lung tissue sections, while Berlin blue staining revealed an abundance of haemosiderin inside alveolar macrophages. In a previous study, a high Fe concentration was detected in alveolar macrophages isolated from the broncho-alveolar lavage fluid of PAP patients , and it was suggested that assessment of lysosomal iron (reflected by the number of haemosiderin-laden alveolar macrophages in bronchoalveolar lavage fluid) might serve as a marker of the progression and prognosis of PAP.
Application of in-air micro-PIXE is possibly useful for evaluation of iron as a disease marker of PAP, assessing the distribution of iron in particles and alveolar macrophages, and for determining the intracellular iron content in alveolar macrophages. Secondary PAP is associated with exposure to inhaled particles and accumulation of iron in alveolar macrophages.
We thank Norio Horiguchi M.D, Gunma University and Hideaki Itoh M.D., Meabashi Red Cross Hospital for facilitation of microscopic analysis. This work was not supported by any grant. None of the authors declare competing financial interests.
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