Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals

Monocytic infiltration in renal interstitium is commonly found surrounding the site of calcium oxalate (CaOx) crystal deposition in the kidney. Monocytes are supposed to eliminate the deposited crystals. However, effects of CaOx crystals on the infiltrating monocytes remain unknown. Therefore, this...

Full description

Saved in:
Bibliographic Details
Main Authors: Nilubon Singhto, Kitisak Sintiprungrat, Supachok Sinchaikul, Shui Tein Chen, Visith Thongboonkerd
Other Authors: Mahidol University
Format: Article
Published: 2018
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/28656
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University
id th-mahidol.28656
record_format dspace
spelling th-mahidol.286562018-09-24T15:53:51Z Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals Nilubon Singhto Kitisak Sintiprungrat Supachok Sinchaikul Shui Tein Chen Visith Thongboonkerd Mahidol University Genomics Research Center, Academia Sinica National Taiwan University Biochemistry, Genetics and Molecular Biology Chemistry Monocytic infiltration in renal interstitium is commonly found surrounding the site of calcium oxalate (CaOx) crystal deposition in the kidney. Monocytes are supposed to eliminate the deposited crystals. However, effects of CaOx crystals on the infiltrating monocytes remain unknown. Therefore, this study investigated the altered cellular proteome of human monocytes in response to interaction with CaOx monohydrate (COM) crystals. After 24-h culture with or without 100 μg/mL COM crystals, U937 cells were harvested and subjected to 2-DE analysis with Deep Purple fluorescence staining (n = 5 gels/group; each was derived from independent culture). Spot matching, quantitative intensity analysis, and statistics revealed 22 differentially expressed proteins (9 up-regulated and 13 down-regulated proteins), which were successfully identified by Q-TOF MS and MS/MS analyses, including those involved in cell cycle, cellular structure, carbohydrate metabolism, lipid metabolism, mRNA processing, and protein synthesis, stabilization, and degradation. Randomly selected changes [up-regulated ALG-2 interacting protein 1 (Alix), elongation factor-2 (EF-2), and down-regulated β-actin] were confirmed by Western blot analysis. Our data may help to understand how monocytes interact with COM crystals. These processes are proposed to cause subsequent inflammatory response in kidney stone disease through oxidative stress pathway(s). © 2010 American Chemical Society. 2018-09-24T08:43:32Z 2018-09-24T08:43:32Z 2010-08-06 Article Journal of Proteome Research. Vol.9, No.8 (2010), 3980-3988 10.1021/pr100174a 15353907 15353893 2-s2.0-77955456260 https://repository.li.mahidol.ac.th/handle/123456789/28656 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955456260&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Nilubon Singhto
Kitisak Sintiprungrat
Supachok Sinchaikul
Shui Tein Chen
Visith Thongboonkerd
Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
description Monocytic infiltration in renal interstitium is commonly found surrounding the site of calcium oxalate (CaOx) crystal deposition in the kidney. Monocytes are supposed to eliminate the deposited crystals. However, effects of CaOx crystals on the infiltrating monocytes remain unknown. Therefore, this study investigated the altered cellular proteome of human monocytes in response to interaction with CaOx monohydrate (COM) crystals. After 24-h culture with or without 100 μg/mL COM crystals, U937 cells were harvested and subjected to 2-DE analysis with Deep Purple fluorescence staining (n = 5 gels/group; each was derived from independent culture). Spot matching, quantitative intensity analysis, and statistics revealed 22 differentially expressed proteins (9 up-regulated and 13 down-regulated proteins), which were successfully identified by Q-TOF MS and MS/MS analyses, including those involved in cell cycle, cellular structure, carbohydrate metabolism, lipid metabolism, mRNA processing, and protein synthesis, stabilization, and degradation. Randomly selected changes [up-regulated ALG-2 interacting protein 1 (Alix), elongation factor-2 (EF-2), and down-regulated β-actin] were confirmed by Western blot analysis. Our data may help to understand how monocytes interact with COM crystals. These processes are proposed to cause subsequent inflammatory response in kidney stone disease through oxidative stress pathway(s). © 2010 American Chemical Society.
author2 Mahidol University
author_facet Mahidol University
Nilubon Singhto
Kitisak Sintiprungrat
Supachok Sinchaikul
Shui Tein Chen
Visith Thongboonkerd
format Article
author Nilubon Singhto
Kitisak Sintiprungrat
Supachok Sinchaikul
Shui Tein Chen
Visith Thongboonkerd
author_sort Nilubon Singhto
title Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
title_short Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
title_full Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
title_fullStr Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
title_full_unstemmed Proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
title_sort proteome changes in human monocytes upon interaction with calcium oxalate monohydrate crystals
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/28656
_version_ 1763492899221143552