Lueschow Shiloh R, McElroy Steven J
Department of Microbiology and Immunology, University of Iowa, Iowa City, IA, United States.
Stead Family Department of Pediatrics, University of Iowa, Iowa City, IA, United States.
Front Immunol. 2020 Apr 3;11:587. doi: 10.3389/fimmu.2020.00587. eCollection 2020.
Paneth cells were first described in the late 19th century by Gustav Schwalbe and Josef Paneth as columnar epithelial cells possessing prominent eosinophilic granules in their cytoplasm. Decades later there is continued interest in Paneth cells as they play an integral role in maintaining intestinal homeostasis and modulating the physiology of the small intestine and its associated microbial flora. Paneth cells are highly specialized secretory epithelial cells located in the small intestinal crypts of Lieberkühn. The dense granules produced by Paneth cells contain an abundance of antimicrobial peptides and immunomodulating proteins that function to regulate the composition of the intestinal flora. This in turn plays a significant role in secondary regulation of the host microvasculature, the normal injury and repair mechanisms of the intestinal epithelial layer, and the levels of intestinal inflammation. These critical functions may have even more importance in the immature intestine of premature infants. While Paneth cells begin to develop in the middle of human gestation, they do not become immune competent or reach their adult density until closer to term gestation. This leaves preterm infants deficient in normal Paneth cell biology during the greatest window of susceptibility to develop intestinal pathology such as necrotizing enterocolitis (NEC). As 10% of infants worldwide are currently born prematurely, there is a significant population of infants contending with an inadequate cohort of Paneth cells. Infants who have developed NEC have decreased Paneth cell numbers compared to age-matched controls, and ablation of murine Paneth cells results in a NEC-like phenotype suggesting again that Paneth cell function is critical to homeostasis to the immature intestine. This review will provide an up to date and comprehensive look at Paneth cell ontogeny, the impact Paneth cells have on the host-microbial axis in the immature intestine, and the repercussions of Paneth cell dysfunction or loss on injury and repair mechanisms in the immature gut.
19世纪末,古斯塔夫·施瓦尔贝(Gustav Schwalbe)和约瑟夫·帕内特(Josef Paneth)首次将潘氏细胞描述为柱状上皮细胞,其细胞质中含有突出的嗜酸性颗粒。几十年后,人们对潘氏细胞的兴趣持续存在,因为它们在维持肠道内环境稳定以及调节小肠及其相关微生物群落的生理功能中发挥着不可或缺的作用。潘氏细胞是位于小肠利伯kühn隐窝中的高度特化的分泌上皮细胞。潘氏细胞产生的致密颗粒含有大量抗菌肽和免疫调节蛋白,其功能是调节肠道菌群的组成。这反过来又在宿主微血管系统的二次调节、肠上皮层的正常损伤和修复机制以及肠道炎症水平中发挥重要作用。这些关键功能在早产儿未成熟的肠道中可能更为重要。虽然潘氏细胞在人类妊娠中期开始发育,但它们直到接近足月妊娠时才具有免疫能力或达到成年密度。这使得早产儿在最易发生肠道病理(如坏死性小肠结肠炎(NEC))的时期缺乏正常的潘氏细胞生物学功能。由于目前全球10%的婴儿为早产儿,有相当数量的婴儿面临潘氏细胞数量不足的问题。与年龄匹配的对照组相比,患NEC的婴儿潘氏细胞数量减少,而对小鼠潘氏细胞的消融会导致类似NEC的表型,这再次表明潘氏细胞功能对未成熟肠道的内环境稳定至关重要。本综述将全面且最新地探讨潘氏细胞的个体发生、潘氏细胞对未成熟肠道中宿主-微生物轴的影响,以及潘氏细胞功能障碍或缺失对未成熟肠道损伤和修复机制的影响。