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Isolation and characterization of mouse nasal-associated lymphoid tissue
H Asanuma1, A H Thompson, T Iwasaki
1Department of Pathology, National Institute of Health, Tokyo, Japan.
Journal of Immunological Methods
|March 28, 1997
Summary
Researchers developed a new method to isolate mouse nasal-associated lymphoid tissue (NALT). This technique allows for the study of immune responses in the respiratory tract, revealing increased T- and B-cells after influenza infection.
Area of Science:
- Immunology
- Respiratory Tract Research
- Mucosal Immunity
Background:
- Nasal-associated lymphoid tissue (NALT) is a key component of the respiratory tract's mucosal immune system in rodents.
- Understanding NALT's cellular dynamics is crucial for studying upper respiratory tract infections and immune responses.
Purpose of the Study:
- To develop and validate a method for isolating mouse NALT.
- To characterize the cellular composition of NALT in normal and influenza-infected mice.
- To assess the utility of isolated NALT for immunological investigations.
Main Methods:
- Surgical isolation of paired NALT from the palate of mouse upper jaws.
- Flow cytometry (FACScan) analysis of lymphocyte populations (T-cells, B-cells, CD4+, CD8+).
- Culture of NALT lymphocytes to assess cytokine production (IFN-gamma) and antibody secretion (IgA, IgG) post-influenza infection.
Main Results:
- A reproducible method for NALT isolation yielding approximately 3 x 10^5 lymphocytes per fragment.
- NALT lymphocytes in normal mice comprise roughly equal numbers of T- and B-cells, with a CD4+ to CD8+ ratio of 4:1.
- Influenza infection led to a 2-3 fold increase in NALT T- and B-cells, accompanied by increased IFN-gamma production and influenza-specific IgA/IgG antibody secretion.
Conclusions:
- The developed NALT isolation method is effective for immunological studies.
- NALT plays a significant role in the adaptive immune response to respiratory viral infections.
- This method facilitates research into the cellular dynamics of mucosal immunology in the upper respiratory tract.