Science子刊:CD47或可阻止Ptpn6缺陷小鼠的致死性炎症疾病
创作:阿童木 审核:章台柳 01月17日
  • Ptpn6spin小鼠(其SHP1蛋白的208位酪氨酸残基被单一取代成天冬酰胺)会出现炎症脚垫特征的自身炎症性疾病;
  • Ptpn6spin与Cd47-/-小鼠繁殖,后代出生不符合孟德尔比例;
  • Ptpn6spin骨髓细胞移植到Cd47-/-小鼠,导致体重明显下降,随后死亡;
  • Ptpn6缺陷的中性粒细胞促进了Cd47-/-受体小鼠的体重下降和死亡;
  • 此外在患病Cd47-/-小鼠中发现其结肠细胞死亡和肠道渗漏显著增加,使用阿那白滞素阻断IL-1可缓解Cd47-/-小鼠的发病率和死亡率。
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Science Advances近期发表的文章,发现CD47或可改善Ptpn6spin小鼠的致死性炎症疾病,具有保护作用。
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Science Advances [IF:14.957]

CD47 halts Ptpn6-deficient neutrophils from provoking lethal inflammation

CD47阻止Ptpn6缺陷的中性粒细胞引起致命的炎症

10.1126/sciadv.ade3942

01-06, Article

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Mice with SHP1 proteins, which have a single amino acid substitution from tyrosine-208 residue to asparagine (hereafter Ptpn6spin mice), develop an autoinflammatory disease with inflamed footpads. Genetic crosses to study CD47 function in Ptpn6spin mice bred Ptpn6spin × Cd47−/− mice that were not born at the expected Mendelian ratio. Ptpn6spin bone marrow cells, when transferred into lethally irradiated Cd47-deficient mice, caused marked weight loss and subsequent death. At a cellular level, Ptpn6-deficient neutrophils promoted weight loss and death of the lethally irradiated Cd47−/− recipients. We posited that leakage of gut microbiota promotes morbidity and mortality in Cd47−/− mice receiving Ptpn6spin cells. Colonic cell death and gut leakage were substantially increased in the diseased Cd47−/− mice. Last, IL-1 blockade using anakinra rescued the morbidity and mortality observed in the diseased Cd47−/− mice. These data together demonstrate a protective role for CD47 in tempering pathogenic neutrophils in the Ptpn6spin mice.

First Authors:
Lalita Mazgaeen

Correspondence Authors:
Prajwal Gurung

All Authors:
Lalita Mazgaeen,Matthew Yorek,Saurabh Saini,Peter Vogel,David K Meyerholz,Thirumala-Devi Kanneganti,Prajwal Gurung

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