Gomes José Rosa, Ayub Laís Costa, Dos Reis Camila Audrey, Machado Miriam Joice, da Silva Jéssica, Omar Nádia Fayez, de Miranda Soares Maria Albertina
Departament of Molecular, Genetic and Structural Biology, University of Ponta Grossa, Avenue Carlos Cavalcanti, 4748, Ponta Grossa, PR CEP 84030-900, Brazil.
Departament of Molecular, Genetic and Structural Biology, University of Ponta Grossa, Avenue Carlos Cavalcanti, 4748, Ponta Grossa, PR CEP 84030-900, Brazil.
Acta Histochem. 2017 Jan;119(1):71-77. doi: 10.1016/j.acthis.2016.11.010. Epub 2016 Dec 7.
This study aimed to evaluate the temporal and spacial distribution of the mucins produced by goblet cells and intestinal alkaline phosphatase (IAP) expression during the development of the small intestine of the rat. Intestines were removed from rats on the 15th, 17th and 18th days of intratuterine life (i.u.) and on the 3rd, 10th, 17th and 25th days after birth (a.b.). Intestines were processed for routine histological procedures and sections were submitted to histochemistry using PAS to stain neutral glycoproteins and Alcian blue for acidic glycoproteins, as well as immunohistochemistry to detect IAP. In rats, glycoprotein production was seen to begin in the intestinal epithelium cell at around the 17th day of i.u. life; however, this production was not accompanied by morphological indications of the presence of goblet cells. By the 18th i.u. day, the villus epithelium was undergoing differentiation and the first goblet cells could be identified from this time. At around the 10th day a.b., both compartments of the small intestine were detected; i.e. the villi and the crypts. At this timepoint, goblet cells were present in the villi, and also in the upper regions of the crypts. On the 3rd, 10th 17th and 25th days a.b., the presence of the goblet cells increased and presented regional differences in the sections evaluated. IAP was not detected during i.u. life, but was weakly detected in the cells of the villi from the 3rd day a.b., along the entire extension of the villi. On the 10th day, IAP was detected at the tip of the villi, while on the 25th day, it was detected along the extension of the villi, but with a weaker intensity. In conclusion, a temporal and spacial distribution of goblet cells and IAP activity occurs during the development of the small intestine, suggesting a possible regulatory control in accordance with the suckling and weaning phases of food intake in the rat's life.
本研究旨在评估大鼠小肠发育过程中杯状细胞产生的黏蛋白的时空分布以及肠碱性磷酸酶(IAP)的表达情况。在大鼠子宫内生活的第15、17和18天以及出生后第3、10、17和25天取出小肠。对小肠进行常规组织学处理,切片进行组织化学检测,使用过碘酸希夫(PAS)染色检测中性糖蛋白,阿尔辛蓝染色检测酸性糖蛋白,同时进行免疫组织化学检测IAP。在大鼠中,糖蛋白的产生在子宫内生活约第17天时可见于肠上皮细胞;然而,这种产生并未伴随着杯状细胞存在的形态学迹象。到子宫内生活第18天时,绒毛上皮正在分化,此时可识别出第一批杯状细胞。出生后约第10天时,检测到小肠的两个部分,即绒毛和隐窝。此时,绒毛以及隐窝上部区域存在杯状细胞。在出生后第3、10、17和25天,杯状细胞的数量增加,且在所评估的切片中呈现出区域差异。在子宫内生活期间未检测到IAP,但从出生后第3天开始在绒毛细胞中可微弱检测到IAP,且沿绒毛全长均有。在第10天时,在绒毛顶端检测到IAP,而在第25天时,沿绒毛全长均可检测到,但强度较弱。总之,在小肠发育过程中存在杯状细胞和IAP活性的时空分布,这表明可能根据大鼠生命中的哺乳和断奶摄食阶段进行调节控制。