Syndecan-4 deficiency leads to high mortality of lipopolysaccharide-injected mice

被引:109
作者
Ishiguro, K
Kadomatsu, K
Kojima, T
Muramatsu, H
Iwase, M
Yoshikai, Y
Yanada, M
Yamamoto, K
Matsushita, T
Nishimura, M
Kusugami, K
Saito, H
Muramatsu, T
机构
[1] Nagoya Univ, Sch Med, Dept Biochem, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Sch Med, Dept Internal Med 1, Showa Ku, Nagoya, Aichi 4668550, Japan
[3] Nagoya Univ, Sch Med,Res Inst Dis Mechanism & Control, Lab Host Def & Germfree Life, Showa Ku, Nagoya, Aichi 4668550, Japan
[4] Nagoya Univ, Sch Med, Inst Lab Anim Res, Showa Ku, Nagoya, Aichi 4668550, Japan
[5] Nagoya Univ, Sch Hlth Sci, Dept Med Technol, Higashi Ku, Nagoya, Aichi 4618673, Japan
[6] Nagoya Natl Hosp, Naka Ku, Nagoya, Aichi 4600001, Japan
关键词
D O I
10.1074/jbc.M106268200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Syndecan-4 is a transmembrane heparan sulfate proteoglycan belonging to the syndecan family. Following intraperitoneal injection of lipopolysaccharide (LPS), syndecan-4-deficient mice exhibited high mortality compared with wild-type controls. Severe endotoxin shock was observed in the deficient mice: systolic blood pressure and left ventricular fractional shortening were lower in the deficient mice than in the wild-type controls 9 h after LPS injection. Although histological examinations revealed no apparent differences between two groups, the plasma level of interleukin (IL)-1 beta was higher in the deficient mice than in the wild-type controls 9 h after LPS injection. Consistent with the regulatory roles of syndecan-4, its expression in monocytes and endothelial cells of microvasculature increased in the wild-type mice after LPS administration. Although IL-1 beta was produced to the same extent by macrophages from syndecan-4-deficient and wild-type mice after LPS stimulation, inhibition of its production by transforming growth factor-beta1 was impaired in the syndecan-4-deficient macropbages. These results indicate that syndecan-4 could be involved in prevention of endotoxin shock, at least partly through the inhibitory action of transforming growth factor-beta1 on IL-1 beta production.
引用
收藏
页码:47483 / 47488
页数:6
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