Cutting edge: A novel chemokine ligand for CCR10 and CCR3 expressed by epithelial cells in mucosal tissues

被引:242
作者
Pan, JL
Kunkel, EJ
Gosslar, U
Lazarus, N
Langdon, P
Broadwell, K
Vierra, MA
Genovese, MC
Butcher, EC [1 ]
Soler, D
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Lab Immunol & Vasc Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
[4] Vet Affairs Palo Alto Hlth Care Syst, Ctr Mol Biol & Med, Palo Alto, CA 94304 USA
[5] Millenium Pharmaceut, Cambridge, MA 02142 USA
关键词
D O I
10.4049/jimmunol.165.6.2943
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucosae-associated epithelial chemokine (MEC) is a novel chemokine whose mRNA is most abundant in salivary gland, with strong expression in other mucosal sites, including colon, trachea, and mammary gland. MEC is constitutively expressed by epithelial cells; MEC mRNA is detected in cultured bronchial and mammary gland epithelial cell lines and in epithelia isolated from salivary gland and colon using laser capture microdissection, but not in the endothelial, hemolymphoid, or fibroblastic cell lines tested. Although MEC is poorly expressed in skin, its closest homologue is the keratinocyte-expressed cutaneous T cell-attracting chemokine (CTACK; CCL27), and MEC supports chemotaxis of transfected lymphoid cells expressing CCR10, a known CTACK receptor. In contrast to CTACK, however, MEC also supports migration through CCR3, Consistent with this, MEC attracts eosinophils in addition to memory lymphocyte subsets. These results suggest an important role for MEC in the physiology of extracutaneous epithelial tissues, including diverse mucosal organs.
引用
收藏
页码:2943 / 2949
页数:7
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