Searching the Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

 PMID:19808259  

T-bet-dependent S1P5 expression in NK cells promotes egress from lymph nodes and bone marrow.

Craig N Jenne | Anselm Enders | Richard Rivera | Susan R Watson | Alexander J Bankovich | Joao P Pereira | Ying Xu | Carla M Roots | Joshua N Beilke | Arnob Banerjee | Steven L Reiner | Sara A Miller | Amy S Weinmann | Chris C Goodnow | Lewis L Lanier | Jason G Cyster | Jerold Chun
The Journal of experimental medicine | 2009

During a screen for ethylnitrosourea-induced mutations in mice affecting blood natural killer (NK) cells, we identified a strain, designated Duane, in which NK cells were reduced in blood and spleen but increased in lymph nodes (LNs) and bone marrow (BM). The accumulation of NK cells in LNs reflected a decreased ability to exit into lymph. This strain carries a point mutation within Tbx21 (T-bet), which generates a defective protein. Duane NK cells have a 30-fold deficiency in sphingosine-1-phosphate receptor 5 (S1P5) transcript levels, and S1P5-deficient mice exhibit an egress defect similar to Duane. Chromatin immunoprecipitation confirms binding of T-bet to the S1pr5 locus. S1P-deficient mice exhibit a more severe NK cell egress block, and the FTY720-sensitive S1P1 also plays a role in NK cell egress from LNs. S1P5 is not inhibited by CD69, a property that may facilitate trafficking of activated NK cells to effector sites. Finally, the accumulation of NK cells within BM of S1P-deficient mice was associated with reduced numbers in BM sinusoids, suggesting a role for S1P in BM egress. In summary, these findings identify S1P5 as a T-bet-induced gene that is required for NK cell egress from LNs and BM.

Pubmed ID: 19808259

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: AI52127
  • Agency: NIDA NIH HHS, United States
    Id: DA019674
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI076458-02
  • Agency: PHS HHS, United States
    Id: BAA-NIH-NIAID-DAIT-07-35
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI052127
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI042370-12
  • Agency: PHS HHS, United States
    Id: T3207270
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI042370
  • Agency: NIAID NIH HHS, United States
    Id: AI74847
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA019674
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI076458
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI061061
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI074847
  • Agency: NIAID NIH HHS, United States
    Id: R56 AI061061
  • Agency: NIAID NIH HHS, United States
    Id: AI061061

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


GENO3D (tool)

RRID:SCR_003183

An automatic web server for protein molecular modelling. Starting with a query protein sequence, the server performs the homology modelling in six successive steps: (i) identify homologous proteins with known 3D structures by using PSI-BLAST; (ii) provide the user all potential templates through a very convenient user interface for target selection; (iii) perform the alignment of both query and subject sequences; (iv) extract geometrical restraints (dihedral angles and distances) for corresponding atoms between the query and the template; (v) perform the 3D construction of the protein by using a distance geometry approach and (vi) finally send the results by e-mail to the user. The strategy used in Geno3D is comparative protein structure modelling by spatial restraints (distances and dihedral) satisfaction.

View all literature mentions

C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

View all literature mentions

CBA/J (tool)

RRID:IMSR_JAX:000656

Mus musculus with name CBA/J from IMSR.

View all literature mentions

C57BL/10 (tool)

RRID:MGI:2159788

laboratory mouse with name C57BL/10 from MGI.

View all literature mentions