Mallow E B, Harris A, Salzman N, Russell J P, DeBerardinis R J, Ruchelli E, Bevins C L
Division of Human Genetics, The Children's Hospital of Philadelphia, Pennsylvania, 19104, USA.
J Biol Chem. 1996 Feb 23;271(8):4038-45. doi: 10.1074/jbc.271.8.4038.
Paneth cells, secretory epithelial cells of the small intestinal crypts, are proposed to contribute to local host defense. Both mouse and human Paneth cells express a collection of antimicrobial proteins, including members of a family of antimicrobial peptides named defensins. In this study, data from an anchored polymerase chain reaction (PCR) strategy suggest that only two defensin mRNA isoforms are expressed in the human small intestine, far fewer than the number expressed in the mouse. The two isoforms detected by this PCR approach were human defensin family members, HD-5 and HD-6. The gene encoding HD-6 was cloned and characterized. HD-6 has a genomic organization similar to HD-5, and the two genes have a striking pattern of sequence similarity localized chiefly in their proximal 5'-flanking regions. Analysis of human fetal RNA by reverse transcriptase-PCR detected enteric defensin HD-5 mRNA at 13.5 weeks of gestation in the small intestine and the colon, but by 17 weeks HD-5 was restricted to the small intestine. HD-6 mRNA was detectable at 13.5-17 weeks of gestation in the small intestine but not in the colon. This pattern of expression coincides with the previously described appearance of Paneth cells as determined by ultrastructural approaches. Northern analysis of total RNA from small intestine revealed quantifiable enteric defensin mRNA in five samples from 19 24 weeks of gestation at levels approximately 40-250-fold less than those observed in the adult, with HD-5 mRNA levels greater than those of HD-6 in all samples. In situ hybridization analysis localized expression of enteric defensin mRNA to Paneth cells at 24 weeks of gestation, as is seen in the newborn term infant and the adult. Consistent with earlier morphological studies, the ratio of Paneth cell number per crypt was reduced in samples at 24 weeks of gestation compared with the adult, and this lower cell number partially accounts for the lower defensin mRNA levels as determined by Northern analysis. Low levels of enteric defensin expression in the fetus may be characteristic of an immaturity of local defense, which is thought to predispose infants born prematurely to infection from intestinal microorganisms.
潘氏细胞是小肠隐窝的分泌性上皮细胞,被认为有助于局部宿主防御。小鼠和人类的潘氏细胞都表达一系列抗菌蛋白,包括一个名为防御素的抗菌肽家族的成员。在本研究中,来自锚定聚合酶链反应(PCR)策略的数据表明,人类小肠中仅表达两种防御素mRNA亚型,远少于小鼠中表达的数量。通过这种PCR方法检测到的两种亚型是人类防御素家族成员HD-5和HD-6。编码HD-6的基因被克隆并进行了表征。HD-6的基因组结构与HD-5相似,这两个基因具有显著的序列相似模式,主要位于它们的近端5'侧翼区域。通过逆转录PCR分析人类胎儿RNA,在妊娠13.5周时在小肠和结肠中检测到肠道防御素HD-5 mRNA,但到17周时HD-5仅限于小肠。HD-6 mRNA在妊娠13.5 - 17周时在小肠中可检测到,但在结肠中未检测到。这种表达模式与先前通过超微结构方法确定的潘氏细胞出现情况一致。对小肠总RNA的Northern分析显示,在妊娠19 - 24周的五个样本中可定量的肠道防御素mRNA水平比成人中观察到的水平低约40 - 250倍,在所有样本中HD-5 mRNA水平均高于HD-6。原位杂交分析将肠道防御素mRNA的表达定位到妊娠24周时的潘氏细胞,这在足月新生儿和成人中也可见。与早期形态学研究一致,与成人相比,妊娠24周样本中每个隐窝的潘氏细胞数量比例降低,这种较低的细胞数量部分解释了Northern分析确定的较低防御素mRNA水平。胎儿中肠道防御素表达水平低可能是局部防御不成熟的特征,这被认为使早产婴儿易受肠道微生物感染。