Interactions of dendritic cells with fibronectin and endothelial cells

被引:0
|
作者
Jancic, C [1 ]
Chuluyan, HE [1 ]
Morelli, A [1 ]
Larregina, A [1 ]
Kolkowski, E [1 ]
Saracco, M [1 ]
Barboza, M [1 ]
Leiva, WS [1 ]
机构
[1] Univ Buenos Aires, Lab Inmunogenet, Hosp Clin, Sch Med, RA-1120 Buenos Aires, DF, Argentina
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied the phenotypic characteristics of spontaneously migrated skin dendritic cells (sDC) and monocyte-derived dendritic cells (moDC), generated under different culture conditions, and their interactions with fibronectin (FN) and endothelial cells. Monocyte-derived dendritic cells were obtained after culturing monocytes with granulocyte-macrophage colony-stimulating factor (GM-CSF) (800 U/ml) and interleukin-4 (IL-4) (500 U/ml) with either 10% fetal bovine serum (FBS) or 10% allogeneic human serum (HS). Regardless of the type of serum used: the majority of moDC expressed human leucocyte antigen-DR (HLA-DR) and CD86. On day 5 of incubation, 20-67% of moDC cultured in the presence of HS (HS-moDC) expressed CD1a, b and c versus 94-97% when cultured in the presence of FBS (FBS-moDC). DC showed a differential gradient of adhesion to FN: FBS-moDC > HS-moDC > sDC a monocytes. Both FBS-moDC and HS-moDC were strongly positive for CD49e (alpha 5-integrin) and CD29 (beta 1-integrin) but negative for CD49d (alpha 4-integrin). A monoclonal antibody (mAb) against CD49e blocked the adhesion of both types of moDC to FN. Although both FBS-moDC and HS moDC attached to endothelium (a 76% and 63% increase, respectively), only HS-moDC were able to migrate through non-activated endothelium. Overall, these results suggest that spontaneously migrated sDC are less adherent to FN than moDC, that HS and FBS induce differences in CD1 expression, that HS-moDC are less adhesive to FN and endothelial cells but more motile than FBS-moDC, and that alpha 5 beta 1-integrin is the molecule involved in moDC adhesion to FN.
引用
收藏
页码:283 / 290
页数:8
相关论文
共 50 条
  • [21] Quantitative analysis of fibronectin fibrillogenesis by endothelial cells on biomaterials
    Pompe, T
    Mitdank, C
    Werner, C
    JOURNAL OF PHYSICS-CONDENSED MATTER, 2004, 16 (26) : S2421 - S2426
  • [22] Modulation of cyclooxygenase in endothelial cells by fibronectin: Relevance to angiogenesis
    Viji, R. I.
    Kumar, V. B. Sameer
    Kiran, M. S.
    Sudhakaran, P. R.
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 105 (01) : 158 - 166
  • [23] CHEMOTACTIC RESPONSE OF VASCULAR ENDOTHELIAL-CELLS TO FIBRONECTIN
    BOWERSOX, JC
    SORGENTE, N
    JOURNAL OF CELL BIOLOGY, 1980, 87 (02): : A64 - A64
  • [24] The interactions between human dendritic cells and microbes; possible clinical applications of dendritic cells
    Kis, Z
    Pallinger, E
    Endresz, V
    Burian, K
    Jelinek, I
    Gonczol, E
    Valyi-Nagy, I
    INFLAMMATION RESEARCH, 2004, 53 (09) : 413 - 423
  • [25] The interactions between human dendritic cells and microbes; possible clinical applications of dendritic cells
    Z. Kis
    E. Pallinger
    V. Endresz
    K. Burian
    I. Jelinek
    E. Gonczol
    I. Valyi-Nagy
    Inflammation Research, 2004, 53 : 413 - 423
  • [26] Interactions of tumor cells with dendritic cells: balancing immunity and tolerance
    M V Dhodapkar
    K M Dhodapkar
    A K Palucka
    Cell Death & Differentiation, 2008, 15 : 39 - 50
  • [27] Interactions of tumor cells with dendritic cells: balancing immunity and tolerance
    Dhodapkar, M. V.
    Dhodapkar, K. M.
    Palucka, A. K.
    CELL DEATH AND DIFFERENTIATION, 2008, 15 (01): : 39 - 50
  • [28] Dendritic cells and T cells: Developmental and functional interactions.
    Shortman, K
    Wu, L
    Kronin, V
    Lucas, K
    Vremec, D
    EXPERIMENTAL HEMATOLOGY, 1998, 26 (08) : 799 - 799
  • [29] Studying interactions between dendritic cells and T cells in vivo
    Chudnovskiy, Aleksey
    Pasqual, Giulia
    Victora, Gabriel D.
    CURRENT OPINION IN IMMUNOLOGY, 2019, 58 : 24 - 30
  • [30] Interactions between dendritic cells and epithelial cells in allergic disease
    Roggen, EL
    Lindstedt, M
    Borrebaeck, C
    Verheyen, GR
    TOXICOLOGY LETTERS, 2006, 162 (01) : 71 - 82