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T Lymphocyte Density and Distribution in Human Colorectal Mucosa, and Inefficiency of Current Cell Isolation Protocols
Mucosal tissues are critical immune effector sites containing complex populations of leukocytes in a tissue microenvironment that remains incompletely understood. We identify and quantify in human distal colorectal tissue absolute mucosal CD3(+) lymphocytes, including CD4(+) and CD8(+) subsets, by d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391713/ https://www.ncbi.nlm.nih.gov/pubmed/25856343 http://dx.doi.org/10.1371/journal.pone.0122723 |
Sumario: | Mucosal tissues are critical immune effector sites containing complex populations of leukocytes in a tissue microenvironment that remains incompletely understood. We identify and quantify in human distal colorectal tissue absolute mucosal CD3(+) lymphocytes, including CD4(+) and CD8(+) subsets, by direct visualization using immunohistochemistry (IHC), immunofluorescence (IF), and an automated counting protocol (r(2)=0.90). Sigmoid and rectal mucosal tissues are both densely packed with T lymphocytes in the mucosal compartment. Both compartments had similar densities of CD3(+) T lymphocytes with 37,400 ± 2,801 cells/mm(3) and 33,700 ± 4,324 cell/mm(3), respectively. Sigmoid mucosa contained 57% CD3(+)CD4(+) and 40% CD3(+)CD8(+) T lymphocytes which calculates to 21,300 ± 1,476/mm(3) and 15,000 ± 275/mm(3) T lymphocytes, respectively. Rectal mucosa had 57% CD3(+)CD4(+) and 42% CD3(+)CD8(+) or 21,577 ± 332, and 17,090 ± 1,206 cells/mm(3), respectively. By comparison, sigmoid mucosal biopsies subjected to conventional collagenase digestion, mononuclear cell (MMC) isolation and staining for flow cytometry yielded 4,549 ± 381/mm(3) and 2,708 ± 245/mm(3) CD4+ and CD8+ T lymphocytes. These data suggest only ~20.7% recovery compared to IHC results for these markers. Further studies will determine if this reflects a selective bias in only CD3(+), CD4(+) and CD8(+) T cells or can be generalized to all flow-analyzed cells from mucosal tissues for phenotyping and functional testing. |
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