4.5 Article

CHRFAM7A reduces monocyte/macrophage migration and colony formation in vitro

期刊

INFLAMMATION RESEARCH
卷 69, 期 7, 页码 631-633

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00011-020-01349-7

关键词

Monocyte migration; Myeloid cell self-renewal; Human-specific genes; alpha 7-nicotinic acetylcholine receptor; Dup alpha 7-nicotinic acetylcholine receptor

资金

  1. NIDCD NIH HHS [5T32DC000028-27] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM121530, 5R01GM121530-03] Funding Source: Medline

向作者/读者索取更多资源

Objective and design CHRFAM7A is a unique human gene that encodes a dominant negative inhibitor of the alpha 7 nicotinic acetylcholine receptor. We have recently shown that CHRFAM7A is expressed in human leukocytes, increases cel-cell adhesion, and regulates the expression of genes associated with leukocyte migration. Material Human THP-1, RAW264.7 and HEK293 cells. Methods Cell migration, cell proliferation and colony formation in soft agar to compare the biological activity of vector vs. CHRFAM7A-transduced cells. Results We show that gene delivery of CHRFAM7A into the THP-1 human monocytic cell line reduces cell migration, reduces chemotaxis to monocyte chemoattractant protein, and reduces colony formation in soft agar. Conclusion Taken together, the findings demonstrate that CHRFAM7A regulates the biological activity of monocytes/macrophages to migrate and undergo anchorage-independent growth in vitro.

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