Human eosinophil cationic protein. Molecular cloning of a cytotoxin and helminthotoxin with ribonuclease activity.
Human eosinophil cationic protein. Molecular cloning of a cytotoxin and helminthotoxin with ribonuclease activity.
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人嗜酸性粒细胞阳离子蛋白。具有核糖核酸酶活性的细胞毒素和螺旋毒素的分子克隆。
DOI:
10.1084/jem.170.1.163
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发表时间:
1989-07-01
影响因子:
15.3
通讯作者:
TENEN, DG
中科院分区:
文献类型:
--
作者:
ROSENBERG, HF;ACKERMAN, SJ;TENEN, DG
We have isolated a 725-bp full-length cDNA clone for the human eosinophil cationic protein (ECP). ECP is a small, basic protein found in the matrix of the eosinophil's large specific granule that has cytotoxic, helminthotoxic, and ribonuclease activity, and is a member of the ribonuclease multigene family. The cDNA sequence shows 89% sequence identity with that reported for the related granule protein, eosinophil-derived neurotoxin (EDN). The open reading frame encodes a previously unidentified 27-amino acid leader sequence preceding a 133- residue mature ECP polypeptide with a molecular mass of 15.6 kD. The encoded amino acid sequence of ECP shows 66% identity to that of EDN and 31% identity to that of human pancreatic ribonuclease, including conservation of the essential structural cysteine and cataytic lysine and histidine residues. mRNA for ECP was detected in eosinophil- enriched peripheral granulocytes and in a subclone of the promyelocytic leukemia line, HL-60, induced toward eosinophilic differentiation with IL-5. No ECP mRNA was detected in uninduced HL-60 cells, or in HL-60 cells induced toward monocytic differentiation with vitamin D3 or toward neutrophilic differentiation with DMSO. In contrast, mRNA for EDN was detected in uninduced HL-60 cells and was upregulated in HL-60 cells induced with DMSO. Despite similarities in sequence and cellular localization, these results suggest that ECP and EDN are subject to different regulatory mechanisms.
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DOI:
10.1073/pnas.83.10.3146
发表时间:
1986-05-01
影响因子:
11.1
作者:
GLEICH, GJ;LOEGERING, DA;MCKEAN, DJ
通讯作者:
MCKEAN, DJ
DOI:
10.1016/s0006-291x(86)80310-2
发表时间:
1986-09-30
影响因子:
3.1
作者:
GULLBERG, U;WIDEGREN, B;OLSSON, I
通讯作者:
OLSSON, I
影响因子:
56.9
作者:
HABERMAN.E
通讯作者:
HABERMAN.E
影响因子:
2.9
作者:
FETT, JW;STRYDOM, DJ;VALLEE, BL
通讯作者:
VALLEE, BL
影响因子:
3.4
作者:
DEGRADO, WF;MUSSO, GF;KEZDY, FJ
通讯作者:
KEZDY, FJ