Neuronal Repellent Slit2 Inhibits Dendritic Cell Migration and the Development of Immune Responses

  • Guan H
  • Zu G
  • Xie Y
  • et al.
77Citations
Citations of this article
49Readers
Mendeley users who have this article in their library.

Abstract

One of the essential functions of dendritic cells is to take up Ags in peripheral tissues and migrate into secondary lymphoid organs to present Ags to lymphocytes for the induction of immune responses. Although many studies have demonstrated that the migration of dendritic cells is closely associated with the development of immune responses, little is known about factors that inhibit dendritic cell migration and control the extent of immune responses to Ag stimulation. We show that Slit2, a neuronal repellent factor, is up-regulated in the skin by allergen sensitization and down-regulates the migration of Langerhans cells. The effect is mediated by direct interaction of Slit2 with cells that express a Slit-specific receptor, Robo1. Slit2-mediated inhibition of Langerhans cell migration results in suppression of contact hypersensitivity responses. These findings provide insights into a novel mechanism by which Slit2 functions as an anti-inflammatory factor for the initiation of immune responses.

Figures

  • Table I. Information of primers applied for determination of Slit mRNA expression by RT-PCR and real time RT-PCR
  • FIGURE 1. Recombinant Slit2 inhibits the hapten-induced migration of Langerhans cells in skin explant culture. Mouse ear skin was treated with hapten (DNFB) before explant culture in medium containing Slit2 or conditioned medium from the parental HEK293 cells. A, At 48 h after initiation of culture, the migration of Langerhans cells was inhibited in culture medium containing Slit2 (10 nM) (Column 1) compared with migration in HEK293-conditioned or fresh medium (Columns 2 and 3) (four ear explants per group). B, The number of Langerhans cells in the epidermis of skin explants (6 per group) was detected by immunohistochemical staining with anti-Ia/IE Ab. The difference between two groups is significant (p 0.01). C, Analysis at 48 h after initiation of culture showed that the inhibitory effect of Slit2 on Langerhans cell migration was dose dependent (eight ear explants per group). D, The time course of the effects of Slit2 (10 nM) on Langerhans cell migration showed a peak at 48 h (four ear explants per group). Data represent the total number of migratory cells in each group and are representative of two to three repeated experiments.
  • FIGURE 3. The inhibitory effect of Slit2 on DC is mediated via a direct interaction with the cells. Bone marrow-derived (BM) DC (A) or Langerhans cell line XS106 (B) were pretreated with Slit2 and then injected s.c. into mice. The migration index of Slit2-treated and untreated control (Ctrl) cells in the draining lymph nodes was evaluated 18–20 h after injection. The migration index of Slit2-pretreated XS106 and bone marrow-derived DC was significantly lower than that of the untreated counterparts (p 0.01). Data represent the average of six mice per group. C, The treatment with Slit2 did not affect the proliferation of XS106 cells (p 0.05). The experiments were repeated two to three times.
  • FIGURE 2. The inhibitory effect of Slit2 on hapten-induced Langerhans cell migration is mediated by the receptor, Robos. Skin explant cultures of DNFB-treated mouse ears were prepared as described in Fig. 1, with the addition of the soluble receptor RoboN in the culture medium. A, The neutralization effect of RoboN is dose dependent, and Langerhans cell migration in the presence of Slit2 can be completely rescued by RoboN. The experiment was repeated twice. B, RoboN (5 nM) neutralizes the activity of endogenous Slits and enhances the migration of Langerhans cells. Standard culture medium (Med) and HEK293-conditioned medium (293) served as controls. The experiment was repeated twice. Results represent the average of eight ear explants per group.
  • FIGURE 4. Slit2 inhibits contact hypersensitivity responses. Purified Slit2, RoboN, or PBS were injected into the dorsal site of one ear. Untreated mice served as control (Ctrl). The injected ear was then painted with the hapten, oxazolone. The other ear was challenged with the same hapten 5 days later, and the ear swelling response was measured. Controls include naive mice that were not sensitized to hapten but were challenged. Slit2 significantly reduced the inflammatory response (p 0.01), whereas application of RoboN heightened the response considerably (p 0.05). Data represent the average of four mice in each group. The experiment was repeated four times.
  • FIGURE 5. Slit2 inhibits the hapten-induced migration of Langerhans cells in vivo. Purified Slit2, RoboN, or PBS was injected into the dorsal site of ears. Mice without injection in the ear served as controls (Ctrl). The injected ear was then painted with oxazolone. The skin samples were harvested 18–20 h later, and Langerhans cells in the epidermis were stained with PE-labeled anti-Ia/IE Ab. Naive skin served as a control. A, Representative photomicrographs of the epidermis of naive, untreated control or Slit2-, PBS-, and RoboN-treated samples. B, The number of Langerhans cells in the epidermis of skin samples was counted. A significant difference in the number of Langerhans cells in Slit2-treated skin samples and the numbers in PBS-, control, or RoboN-treated skin samples was observed (p 0.05). The Langerhans cell numbers represent the average of six ears per group. The experiment was repeated three times.
  • FIGURE 6. Expression of Slits in the skin. A, The reported expression of Slit1, -2, and -3 mRNA in the mouse brain was confirmed. Slit2 mRNA was found to be expressed constitutively in the naive skin and up-regulated at 4, 24, and 48 h after hapten sensitization. Slit1 and Slit3 were not detectable in the naive or hapten-treated skin using this assay. Representative figures are shown from four experiments. B, Slit2 mRNA in the skin was quantitatively determined by real time RT-PCR after sensitization with DFNB. C, In situ hybridization indicated that Slit2 was expressed in the epidermis of sensitized mice but undetectable in naive animals. The specific signal of Slit2 was not detected in the dermis. Sense cRNA served as controls.
  • FIGURE 7. Expression of Robo1 by DC. Cells were stained with chicken anti-Robo1 Ab followed by Cy-3-labeled anti-chicken Ab (red). DAPI was used to stain nucleus (blue). A, The Ab stained RoboN-transfected but not wild-type HEK293 cells. The staining of RoboN-transfected cells with the Ab was diminished by preabsorption with soluble RoboN. B, Anti-Robo1 Ab stained XS106 and bone marrow-derived (BM) DC. Preabsorption of the Ab with RoboN diminished the staining. C, The majority of migratory cells from skin explant cultures were stained by the antiRobo1 Ab. Double staining with anti-Ia/IE Ab (green) showed that most of MHC class IIpositive migratory cells expressed Robo1 (arrows). Some Robo1-positive cells were stained by CD11b Ab (green, arrows).

References Powered by Scopus

Dendritic cells and the control of immunity

12707Citations
N/AReaders
Get full text

Immunobiology of dendritic cells

5835Citations
N/AReaders
Get full text

A novel method for real time quantitative RT-PCR

1824Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Human mesenchymal stem cell subpopulations express a variety of neuro-regulatory molecules and promote neuronal cell survival and neuritogenesis

586Citations
N/AReaders
Get full text

MiR-218 inhibits invasion and metastasis of gastric cancer by targeting the robo1 receptor

411Citations
N/AReaders
Get full text

Netrin-1 inhibits leukocyte migration in vitro and in vivo

238Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Guan, H., Zu, G., Xie, Y., Tang, H., Johnson, M., Xu, X., … Xu, H. (2003). Neuronal Repellent Slit2 Inhibits Dendritic Cell Migration and the Development of Immune Responses. The Journal of Immunology, 171(12), 6519–6526. https://doi.org/10.4049/jimmunol.171.12.6519

Readers over time

‘09‘10‘11‘12‘13‘14‘15‘16‘17‘18‘19‘20‘21‘2402468

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 22

55%

Researcher 12

30%

Professor / Associate Prof. 5

13%

Lecturer / Post doc 1

3%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 17

53%

Medicine and Dentistry 7

22%

Biochemistry, Genetics and Molecular Bi... 4

13%

Immunology and Microbiology 4

13%

Save time finding and organizing research with Mendeley

Sign up for free
0