1.Nuclear Image Analysis Study of Neuroendocrine Tumors.
Meeja PARK ; Taehwa BAEK ; Jongho BAEK ; Hyunjin SON ; Dongwook KANG ; Jooheon KIM ; Hyekyung LEE
Korean Journal of Pathology 2012;46(1):38-41
BACKGROUND: There is a subjective disagreement about nuclear chromatin in the field of pathology. Objective values of red, green, and blue (RGB) light intensities for nuclear chromatin can be obtained through a quantitative analysis using digital images. METHODS: We examined 10 cases of well differentiated neuroendocrine tumors of the rectum, small cell lung carcinomas, and moderately differentiated squamous cell lung carcinomas respectively. For each case, we selected 30 representative cells and captured typical microscopic findings. Using an image analyzer, we determined the longest nuclear line profiles and obtained graph files and Excel data on RGB light intensities. We assessed the meaningful differences in graph files and Excel data among the three different tumors. RESULTS: The nucleus of hematoxylin and eosin-stained tumor cells was expressed as a combination of RGB light sources. The highest intensity was from blue, whereas the lowest intensity was from green. According to the graph files, green showed the most noticeable change in the light intensity, which is consistent with the difference in standard deviations. CONCLUSIONS: The change in the light intensity for green has an important implication for differentiating between tumors. Specific features of the nucleus can be expressed in specific values of RGB light intensities.
Chromatin
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Hematoxylin
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Image Processing, Computer-Assisted
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Light
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Lung
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Neuroendocrine Tumors
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Rectum
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Small Cell Lung Carcinoma
2.Interactions between NCR + ILC3s and the Microbiome in the Airways Shape Asthma Severity
Jongho HAM ; Jihyun KIM ; Sungmi CHOI ; Jaehyun PARK ; Min-gyung BAEK ; Young-Chan KIM ; Kyoung-Hee SOHN ; Sang-Heon CHO ; Siyoung YANG ; Yong-Soo BAE ; Doo Hyun CHUNG ; Sungho WON ; Hana YI ; Hye Ryun KANG ; Hye Young KIM
Immune Network 2021;21(4):e25-
Asthma is a heterogeneous disease whose development is shaped by a variety of environmental and genetic factors. While several recent studies suggest that microbial dysbiosis in the gut may promote asthma, little is known about the relationship between the recently discovered lung microbiome and asthma. Innate lymphoid cells (ILCs) have also been shown recently to participate in asthma. To investigate the relationship between the lung microbiome, ILCs, and asthma, we recruited 23 healthy controls (HC), 42 patients with non-severe asthma, and 32 patients with severe asthma. Flow cytometry analysis showed severe asthma associated with fewer natural cytotoxicity receptor (NCR) + ILC3s in the lung.Similar changes in other ILC subsets, macrophages, and monocytes were not observed. The asthma patients did not differ from the HC in terms of the alpha and beta-diversity of the lung and gut microbiomes. However, lung function correlated positively with both NCR + ILC3 frequencies and microbial diversity in the lung. Sputum NCR + ILC3 frequencies correlated positively with lung microbiome diversity in the HC, but this relationship was inversed in severe asthma. Together, these data suggest that airway NCR + ILC3s may contribute to a healthy commensal diversity and normal lung function.