Quantitative change of IgA hinge O-glycan composition is a novel marker of therapeutic responses of IgA nephropathy

肾病 糖基化 粘蛋白 聚糖 肾小球肾炎 免疫学 发病机制 医学 内科学 生物 内分泌学 糖蛋白 生物化学 病理 糖尿病
作者
Hirotsugu Iwatani,Takahiro Inoue,Yoshinao Wada,Yasuyuki Nagasawa,Ryohei Yamamoto,Hideki Iijima,Tetsuo Takehara,Enyu Imai,Hiromi Rakugi,Yoshitaka Isaka
出处
期刊:Biochemical and Biophysical Research Communications [Elsevier]
卷期号:428 (3): 339-342 被引量:20
标识
DOI:10.1016/j.bbrc.2012.10.049
摘要

Aberrant O-glycosylation in the hinge region of serum IgA is suggested to be involved in the pathogenesis of IgA nephropathy (IgAN), because the hypoglycosylation including N-acetylneuraminic acid or galactose has been reported in the mucin-type O-glycan of the hinge portion (HP) of IgA deposited in the IgAN patients' kidney. These aberrant glycosylation has been assessed in most of the previous reports by qualitative but not quantitative methods. In the present study, the molar ratios of GalNAc or Gal to HP were analyzed for serum IgA from IgAN patients. The GalNAc/HP ratio was increased in the patients who achieved remission after a combination therapy of tonsillectomy and intravenous corticosteroid, suggesting any non-innate factors to affect the IgA O-glycosylation in IgAN that is thought to be inherently determined. Furthermore, the O-glycosylation status was different among three groups: IgAN patients in the pretreatment stage, IgAN patients in the remission stage after treatment and healthy controls. These results indicated that aberrant O-glycosylation of serum IgA in the IgAN patients would be inherently present and, to some extent, affected by therapeutic intervention. Finally, the quantitative change of O-glycan composition is a novel marker of therapeutic response of IgAN.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
sshah完成签到,获得积分20
1秒前
孙希熳完成签到,获得积分20
1秒前
normankasimodo完成签到,获得积分10
1秒前
2秒前
星河长明完成签到,获得积分10
3秒前
4秒前
wang发布了新的文献求助10
5秒前
6秒前
田12发布了新的文献求助10
6秒前
共享精神应助学术小牛采纳,获得10
6秒前
哒哒哒完成签到,获得积分20
6秒前
7秒前
7秒前
7秒前
8秒前
852应助才浅采纳,获得10
8秒前
宋木完成签到,获得积分10
8秒前
9秒前
思源应助HOOW采纳,获得10
9秒前
10秒前
10秒前
齐映雁发布了新的文献求助10
10秒前
11秒前
英吉利25发布了新的文献求助10
11秒前
余雨发布了新的文献求助10
11秒前
11秒前
lu发布了新的文献求助10
12秒前
13秒前
清脆画板发布了新的文献求助10
14秒前
14秒前
mookie发布了新的文献求助10
15秒前
杨宇发布了新的文献求助10
15秒前
16秒前
打打应助liu采纳,获得10
16秒前
丘比特应助蘑菇采纳,获得30
17秒前
简单的易云完成签到,获得积分10
17秒前
缥缈青丝发布了新的文献求助10
17秒前
干净羊青发布了新的文献求助10
18秒前
小马甲应助林间月采纳,获得100
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 3000
Les Mantodea de guyane 2500
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 2000
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
Brittle Fracture in Welded Ships 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5945168
求助须知:如何正确求助?哪些是违规求助? 7097505
关于积分的说明 15898544
捐赠科研通 5077181
什么是DOI,文献DOI怎么找? 2730290
邀请新用户注册赠送积分活动 1690245
关于科研通互助平台的介绍 1614551