Superior isolation of antigen-specific brain infiltrating T cells using manual homogenization technique.
J Immunol Methods
; 439: 23-28, 2016 12.
Article
in En
| MEDLINE
| ID: mdl-27623324
ABSTRACT
Effective recovery of activated brain infiltrating lymphocytes is critical for investigations involving murine neurological disease models. To optimize lymphocyte recovery, we compared two isolation methods using brains harvested from seven-day Theiler's murine encephalomyelitis virus (TMEV) and TMEV-OVA infected mice. Brains were processed using either a manual dounce based approach or enzymatic digestion using type IV collagenase. The resulting cell suspensions from these two techniques were transferred to a percoll gradient, centrifuged, and lymphocytes were recovered. Flow cytometric analysis of CD45hi cells showed greater percentage of CD44hiCD62lo activated lymphocytes and CD19+ B cells using the dounce method. In addition, we achieved a 3-fold greater recovery of activated virus-specific CD8 T cells specific for the immunodominant DbVP2121-130 and engineered KbOVA257-264 epitopes through manual dounce homogenization approach as compared to collagenase digest. A greater percentage of viable cells was also achieved through dounce homogenization. Therefore, we conclude that manual homogenization is a superior approach to isolate activated T cells from the mouse brain.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Brain
/
Lymphocyte Activation
/
Cell Separation
/
Ovalbumin
/
Theilovirus
/
Cardiovirus Infections
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CD8-Positive T-Lymphocytes
/
Antigens
Limits:
Animals
Language:
En
Journal:
J Immunol Methods
Year:
2016
Document type:
Article
Affiliation country:
United States