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Human spleen microanatomy: why mice do not suffice.
1Institute of Anatomy and Cell Biology, University of Marburg, Marburg, Germany.
Immunology
|April 2, 2015
Summary
Human spleen structure differs from rodents, lacking a marginal zone and featuring unique sheathed capillaries. Understanding these microanatomical differences is crucial for studying lymphocyte recirculation in human spleens.
Area of Science:
- Immunology
- Anatomy
- Histology
Background:
- Spleen microanatomy is primarily described in rodents, leading to terminological issues for human studies.
- The spleen comprises white pulp (lymphocytes) and red pulp (blood cells) in mice, rats, and humans.
- Rodent spleens have a distinct marginal zone absent in humans.
Purpose of the Study:
- To review and compare the splenic white and red pulp structure in rats, mice, and humans.
- To highlight species-specific microanatomical differences, particularly in humans.
- To encourage further research into lymphocyte recirculation within the human spleen.
Main Methods:
- Comparative review of microanatomical descriptions of rat, mouse, and human spleens.
- Analysis of histological features, including white pulp, red pulp, and associated vascular structures.
- Examination of cellular composition and organization within splenic compartments.
Main Results:
- Human spleens lack the rodent marginal zone; secondary follicles have germinal, mantle, and superficial zones.
- Human red pulp contains sheathed capillaries, distinct from the ellipsoids found in most vertebrates but absent in rats and mice.
- Human spleens likely possess an open circulation system, with no observed capillary-to-sinus connections in the red pulp.
- Three distinct stromal cell types are identified in the human white pulp.
Conclusions:
- Significant microanatomical differences exist between human and rodent spleens, necessitating species-specific terminology.
- Human splenic microarchitecture, including sheathed capillaries and an open circulation, supports unique lymphocyte trafficking.
- Further investigation into human splenic structure is vital for understanding immune responses and lymphocyte recirculation.
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