Development, alteration and real time dynamics of conjunctiva-associated lymphoid tissue

PLoS One. 2013 Dec 20;8(12):e82355. doi: 10.1371/journal.pone.0082355. eCollection 2013.

Abstract

Purpose: Conjunctiva-associated lymphoid tissue (CALT) is thought to play a key role in initiating ocular surface related immune responses. This study was planned to get first profound insights into the function of CALT related to development, cellular dynamics and morphological alteration using a novel mouse model.

Methods: Expression and morphology of CALT were investigated using BALB/c mice kept under different housing conditions, after topical antigen-stimulation and following lymphadenectomy and splenectomy. Particles and bacteria were applied topically to study antigen-transport. Intravital visualization was performed using two-photon microscopy.

Results: Postnatal development and ultrastructure of CALT in the mouse is similar to humans. Topical antigen-challenge significantly alters CALT expression. Bacterial translocation is demonstrated via lymphoepithelium whereas cellular velocities within follicles were approximately 8 µm/min.

Conclusions: CALT in the mouse is an immunological interface of the ocular surface, featuring dynamic processes such as morphological plasticity, particle/bacteria transport and cellular migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / metabolism
  • Cell Compartmentation
  • Cell Movement
  • Cervical Vertebrae / surgery
  • Computer Systems*
  • Conjunctiva / cytology*
  • Conjunctiva / growth & development*
  • Conjunctiva / ultrastructure
  • Endocytosis
  • Female
  • Housing, Animal
  • Humans
  • Lymph Node Excision
  • Lymphocyte Activation / immunology
  • Lymphoid Tissue / cytology*
  • Lymphoid Tissue / growth & development*
  • Lymphoid Tissue / ultrastructure
  • Mice, Inbred BALB C
  • Receptors, Cell Surface / metabolism
  • Specific Pathogen-Free Organisms
  • T-Lymphocytes / immunology

Substances

  • Antigens
  • Receptors, Cell Surface

Grants and funding

University of Luebeck, Medical faculty grants to PS and GH, GlaxoSmithKline to PS, BVA Sicca Research Grant to SS, UG and PS, Helmut und Ruth Lingen-Stiftung to PS, Koeln Fortune Program/Faculty of Medicine, University of Cologne and Deutsche Forschungsgemeinschaft (DFG) STE1928/2-1 to PS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.