CXCL1
CXCL1(英語:)是一小分子的细胞因子属于CXC趋化因子家族[1]。又被称作生长调节致癌基因α (Growth-regulated oncogene alpha, GROα)[1][2][3]。 趋化因子CXCL1是由巨噬细胞,中性粒细胞和上皮细胞表达的[4][5]。趋化因子CXCL1对中性粒细胞有细胞趋化作用[1]。CXCL1结合到趋化因子受体CXCR2上而起细胞趋化作用[6]。人类的CXCL1与许多CXC类的趋化因子基因相邻聚集在第四染色体上[7] 。CXCL1的主要作用包括新血管形成、炎症反应、伤口愈合[6]和肿瘤形成[2][3]。
Chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha) | |||||||||||||
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PDB rendering based on 1mgs. | |||||||||||||
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标识 | |||||||||||||
代号 | CXCL1; FSP; GRO1; GROa; MGSA; MGSA-a; NAP-3; SCYB1 | ||||||||||||
扩展标识 | 遗传学:155730 鼠基因:3037818 同源基因:117693 GeneCards: CXCL1 Gene | ||||||||||||
直系同源体 | |||||||||||||
物种 | 人类 | 小鼠 | |||||||||||
Entrez | 2919 | 330122 | |||||||||||
Ensembl | ENSG00000163739 | ENSMUSG00000029379 | |||||||||||
UniProt | P09341 | Q6W5C0 | |||||||||||
mRNA序列 | NM_001511 | NM_203320 | |||||||||||
蛋白序列 | NP_001502 | NP_976065 | |||||||||||
基因位置 |
Chr 4: 74.74 – 74.74 Mb |
Chr 5: 90.79 – 90.79 Mb | |||||||||||
PubMed查询 | |||||||||||||
参见
- CXCR2
- 趋化因子
参考文献
- Moser B, Clark-Lewis I, Zwahlen R, Baggiolini M. Neutrophil-activating properties of the melanoma growth-stimulatory activity. J Exp Med. 1990 May 1;171(5):1797-802.
- Anisowicz, A., Bardwell, L., Sager, R. Constitutive overexpression of a growth-regulated gene in transformed Chinese hamster and human cells. Proc. Nat. Acad. Sci. 84: 7188-7192, 1987.
- Richmond, A., Thomas, H. G. (1988) Melanoma growth stimulatory activity: isolation from human melanoma tumors and characterization of tissue distribution J. Cell. Biochem. 36,185-198
- Iida N, Grotendorst GR. Cloning and sequencing of a new gro transcript from activated human monocytes: expression in leukocytes and wound tissue. Mol Cell Biol. 1990 Oct;10(10):5596-9.
- Becker S, Quay J, Koren HS, Haskill JS. Constitutive and stimulated MCP-1, GRO alpha, beta, and gamma expression in human airway epithelium and bronchoalveolar macrophages. Am J Physiol. 1994 Mar;266(3 Pt 1):L278-86.
- Devalaraja, R. M., Nanney, L. B., Du, J., Qian, Q., Yu, Y., Devalaraja, M. N., Richmond, A. (2000) Delayed wound healing in CXCR2 knockout mice J. Investig. Dermatol. 115,234-244
- Richmond A, Balentien E, Thomas HG, Flaggs G, Barton DE, Spiess J, Bordoni R, Francke U, Derynck R. Molecular characterization and chromosomal mapping of melanoma growth stimulatory activity, a growth factor structurally related to beta-thromboglobulin. EMBO J. 1988 Jul;7(7):2025-33.
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