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犬T细胞共刺激分子(CD28)的分子克隆与测序

Molecular cloning and sequencing of canine T-cell costimulatory molecule (CD28).

作者信息

Khatlani T S, Ma Z, Okuda M, Onishi T

机构信息

Laboratory of Veterinary Internal Medicine, Faculty of Agriculture, Yamaguchi University, 1677-1 Yoshida, Yamagughi 753-8515, Japan.

出版信息

Vet Immunol Immunopathol. 2001 Feb 10;78(3-4):341-8. doi: 10.1016/s0165-2427(01)00238-0.

DOI:10.1016/s0165-2427(01)00238-0
PMID:11292534
Abstract

T-cells express CD28 and CTLA-4, and through binding to their shared ligands (CD80/CD86) on antigen presenting cells, provide a potent co-stimulatory signal for T-cell activation and proliferation. To investigate the role of CD28 in canine immune system, we hereby report the molecular cloning and sequencing of the full-length complementary DNA (cDNA) coding for canine CD28, from pokeweed mitogen stimulated canine peripheral blood lymphocytes. The cloned cDNA contains an open reading frame of 663 nucleotides, encoding for a polypeptide of 221 amino acids. The amino acid sequence of the canine CD28 showed 91.9, 80, and 79.6% similarities with those of the cat, cattle, and human counterparts, respectively. Five sequence motifs of TATT or ATTTA involved in the regulation of gene expression by influencing mRNA stability are found in the 3' untranslated region. The hexapeptide motif (MYPPPY), five cysteine residues, a potential N-glycosylation site and a cytoplasmic phosphatidylinositol 3-kinase binding site in canine CD28 molecule are completely conserved in canine CTLA-4. The availability of full length canine CD28 will provide a useful molecule for studying its role in dog immune system.

摘要

T细胞表达CD28和CTLA-4,通过与抗原呈递细胞上它们的共同配体(CD80/CD86)结合,为T细胞活化和增殖提供强大的共刺激信号。为了研究CD28在犬免疫系统中的作用,我们在此报告从商陆丝裂原刺激的犬外周血淋巴细胞中克隆并测序编码犬CD28的全长互补DNA(cDNA)。克隆的cDNA包含一个663个核苷酸的开放阅读框,编码一个221个氨基酸的多肽。犬CD28的氨基酸序列与猫、牛和人类相应序列分别显示出91.9%、80%和79.6%的相似性。在3'非翻译区发现了五个TATT或ATTTA序列基序,它们通过影响mRNA稳定性参与基因表达的调控。犬CD28分子中的六肽基序(MYPPPY)、五个半胱氨酸残基、一个潜在的N-糖基化位点和一个细胞质磷脂酰肌醇3-激酶结合位点在犬CTLA-4中完全保守。全长犬CD28的可得性将为研究其在犬免疫系统中的作用提供一个有用的分子。

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1
Molecular cloning and sequencing of canine T-cell costimulatory molecule (CD28).犬T细胞共刺激分子(CD28)的分子克隆与测序
Vet Immunol Immunopathol. 2001 Feb 10;78(3-4):341-8. doi: 10.1016/s0165-2427(01)00238-0.
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Complementarity determining region 1 (CDR1)- and CDR3-analogous regions in CTLA-4 and CD28 determine the binding to B7-1.细胞毒性T淋巴细胞相关抗原4(CTLA-4)和CD28中互补决定区1(CDR1)及CDR3类似区域决定了与B7-1的结合。
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Cattle CTLA-4, CD28 and chicken CD28 bind CD86: MYPPPY is not conserved in cattle CD28.牛的细胞毒性T淋巴细胞相关抗原4(CTLA-4)、细胞毒性T淋巴细胞相关抗原28(CD28)以及鸡的CD28均可结合CD86:牛CD28中不保守存在“MYPPPY”序列。
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The cytoplasmic domain of CD28 is both necessary and sufficient for costimulation of interleukin-2 secretion and association with phosphatidylinositol 3'-kinase.CD28的胞质结构域对于共刺激白细胞介素-2的分泌以及与磷脂酰肌醇3'-激酶的结合而言,既是必要的也是充分的。
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Cytotoxic T lymphocyte-associated molecule-4, a high-avidity receptor for CD80 and CD86, contains an intracellular localization motif in its cytoplasmic tail.细胞毒性T淋巴细胞相关分子4是一种与CD80和CD86具有高亲和力的受体,其胞质尾部含有一个细胞内定位基序。
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Activation of human peripheral blood dendritic cells induces the CD86 co-stimulatory molecule.人类外周血树突状细胞的激活可诱导共刺激分子CD86的产生。
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Expression of costimulatory molecules CD80 and CD86 and their receptors CD28, CTLA-4 on malignant ascites CD3+ tumour-infiltrating lymphocytes (TIL) from patients with ovarian and other types of peritoneal carcinomatosis.共刺激分子CD80和CD86及其受体CD28、CTLA-4在卵巢癌及其他类型腹膜癌患者恶性腹水中CD3⁺肿瘤浸润淋巴细胞(TIL)上的表达。
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