Belz G T, Heath T J
Department of Anatomical Sciences, University of Queensland, Brisbane, Australia.
Anat Rec. 1996 May;245(1):102-13. doi: 10.1002/(SICI)1097-0185(199605)245:1<102::AID-AR15>3.0.CO;2-T.
Tonsils of the soft palate are especially important in pigs as the major pharyngeal mucosal-associated lymphoid tissue and as a portal of entry for microorganisms. They play a key role in initiating immune responses against antigens entering tonsillar crypts from the oropharynx. The aim of this study was to describe the architecture of the tonsillar crypst and the morphology of their epithelial surface.
Tissue taken from the tonsil of the soft palate of freshly-killed pigs was examined using light microscopy, electron microscopy, and three-dimensional reconstruction techniques.
Tonsils of the soft palate in pigs are penetrated by numerous crypts which extend into, and branch extensively within, the lymphoid tissue. Stratified squamous non-keratinised epithelium covering the oropharyngeal surface is continuous with that lining the neck of crypts. Lymphoepithelium covers the tonsillar lymphoid tissue within the crypts. It consists of non-keratinised epithelial cells, M cells, goblet cells and many intraepithelial lymphoid cells. M cells have a variable surface morphology: some are covered by relatively regular and well-formed microvilli; others possess very long undulant microvilli emanating from broad membranous folds.
Variations in M cell surface morphology occur and these may reflect alterations of the apical plasmalemma in response to antigenic stimuli. Further investigation will be required to determine molecular specializations of the apical membrane of M cells which may facilitate interactions with antigenic material.
软腭扁桃体在猪体内尤为重要,它是主要的咽黏膜相关淋巴组织,也是微生物的侵入门户。它们在启动针对从口咽进入扁桃体隐窝的抗原的免疫反应中起关键作用。本研究的目的是描述扁桃体隐窝的结构及其上皮表面的形态。
使用光学显微镜、电子显微镜和三维重建技术检查从刚宰杀的猪的软腭扁桃体获取的组织。
猪的软腭扁桃体有许多隐窝,这些隐窝延伸至淋巴组织内并在其中广泛分支。覆盖口咽表面的复层鳞状非角化上皮与隐窝颈部的内衬上皮连续。淋巴细胞上皮覆盖隐窝内的扁桃体淋巴组织。它由非角化上皮细胞、M细胞、杯状细胞和许多上皮内淋巴细胞组成。M细胞具有可变的表面形态:一些被相对规则且形态良好的微绒毛覆盖;另一些则具有从宽阔的膜褶发出的非常长的波浪状微绒毛。
M细胞表面形态存在差异,这些差异可能反映顶端质膜对抗抗原刺激的改变。需要进一步研究以确定M细胞顶端膜的分子特化,这可能有助于与抗原物质的相互作用。