4.5 Article

Proteomic analyses reveal that immune integrins are major targets for regulation by Membrane-Associated Ring-CH (MARCH) proteins MARCH2, 3, 4 and 9

期刊

PROTEOMICS
卷 21, 期 11-12, 页码 -

出版社

WILEY
DOI: 10.1002/pmic.202000244

关键词

B‐ cells; cell surface; Integrins; MARCH

资金

  1. National Health and Medical Research Council of Australia [1113577, 1099752, 1078737, 1058344, 1121755]
  2. NHMRC IRISS scheme grant [9000220]
  3. Victorian State Government Operational Infrastructure Scheme grant
  4. National Health and Medical Research Council of Australia [1121755, 1099752, 9000220, 1078737] Funding Source: NHMRC

向作者/读者索取更多资源

Research showed that MARCH proteins regulate the expression of immune response-related receptors and affect various cell surface proteins, including integrin complexes crucial for immune cell homing, adhesion, and migration.
MARCH proteins are membrane-associated Ring-CH E3 ubiquitin ligases that dampen immune responses by downregulating cell surface expression of major histocompatibility complexes I and II as well as immune co-stimulatory receptors. We recently showed that MARCH2,3,4 and 9 also downregulate cell surface expression of the inflammatory cytokine receptor for interleukin-6 (IL6R alpha). Here we use over-expression of these MARCH proteins in the M1 myeloid leukaemia cell line and cell surface proteomic analyses to globally analyse other potential targets of these proteins. A large range of cell surface proteins regulated by more than one MARCH protein in addition to several MARCH protein-specific cell surface targets were identified most of which were downregulated by MARCH expression. Prominent among these were several integrin complexes associated with immune cell homing, adhesion and migration. Integrin alpha 4 beta 1 (VLA4 or VCAM-1 receptor) was downregulated only by MARCH2 and we showed that in MARCH2 knockout mice, Integrin alpha 4 was upregulated specifically in mature B-lymphocytes and this was accompanied by decreased numbers of B-cells in the spleen.

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