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Glycosylation on Urinary Exosome for Biomarker Discovery

첫 페이지 보기
  • 발행기관
    한국당과학회 바로가기
  • 간행물
    한국당과학회 학술대회 바로가기
  • 통권
    2013 한국당과학회 동계학술대회 (2013.02)바로가기
  • 페이지
    pp.52-52
  • 저자
    Nayoung Yun, Seunghyup Jeong, Pyong-Gon Moon, Moon Chang Baek, Hyun Joo An
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A212714

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원문정보

초록

영어
IgA Nephropathy (IgAN) and thin basement membrane nephropathy (TBMN) have identical hematuria symptom but different seriousness in renal function. In case of TBMN, renal function is usually normal but IgAN is the most common cause of end-stage renal failure. In general, the biopsy of the kidney is performed to distinguish between IgAN and TBMN. There are a lot of needs for clinicians to have a sensitive and specific biomarker for differentiation IgAN and TBMN. Exosomes which are small cell-derived vesicles have been suggested as potential biomarkers in diagnosis of disease because these are secreted from original cell with intracellular fluids and apical membrane. Urinary exosomes, 40-100nm vesicles secreted to urine by renal cells, may provide non-invasive diagnosis manner of kidney disease. Glycosylation is highly sensitive to the biological environment changes and considerably affected by disease states. Glycan is known as playing key roles in cancer metastasis and intracellular recognition. Therefore, the examination of glycosylation change in urinary exosome may be a new way for potential biomarkers to differentiate TBMN and IgAN. In this study, we have analyzed 18 individuals exosomes secreted into urine from renal epithelial cells. Samples were composed of three different groups, mainly TBMN, IgAN patients, and healthy volunteers. Briefly, N-glycans from urinary exosomes were released by PNGase F digestion and then enriched by solid phase extraction using a porous graphitized carbon cartridge. N-glycans were eluted with three different solution (10% ACN, 20% ACN, and 40% ACN with 0.05% TFA in H2O) based on the glycan size and polarity. Enriched glycans were analyzed for qualitative and quantitative profiling using high resolution MALDI-TOF/TOF mass spectrometry and performed tandem MS to obtain extensive structure information. We also separated isomer-specific glycans by nano-LC chip/Q-TOF mass spectrometry. We found that high mannose glycans are high in abundance in normal group. Complex, non-sialylated fucosylated tri-, and tetraantennary glycans are significantly different between normal and patients, which suggest the potential biomarker.

저자

  • Nayoung Yun [ Graduate School of Analytical Science Technology, Chungnam National University, Daejeon, Korea ]
  • Seunghyup Jeong [ Graduate School of Analytical Science Technology, Chungnam National University, Daejeon, Korea ]
  • Pyong-Gon Moon [ Department of Molecular Medicine, School of Medicine, Kyungpook National University, Daegu, Korea ]
  • Moon Chang Baek [ Department of Molecular Medicine, School of Medicine, Kyungpook National University, Daegu, Korea ]
  • Hyun Joo An [ Graduate School of Analytical Science Technology, Chungnam National University, Daejeon, Korea ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국당과학회 [Korean Society for Glycoscience]
  • 설립연도
    2006
  • 분야
    의약학>약학
  • 소개
    본 학회는 화학, 생화학, 분자생물학, 미생물학, 식품공학, 의학, 약학, 유전공학 및 생물공학, 환경 및 기타 공업 등 전 분야의 탄수화물관련 이론과 기술을 연구 발전시키고 산학협동을 통해 이를 보급하여 국내 관련 산업의 발전 및 국민생활의 과학화에 기여하고자 하며, 이러한 목표와 비젼의 실현을 위해 회원들이 적극적인 참여와 활동을 전개하고자 한다.

간행물

  • 간행물명
    한국당과학회 학술대회
  • 간기
    연간
  • 수록기간
    2006~2022
  • 십진분류
    KDC 517 DDC 614

이 권호 내 다른 논문 / 한국당과학회 학술대회 2013 한국당과학회 동계학술대회

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