Mullol J, Rieves R D, Baraniuk J N, Lundgren J D, Mérida M, Hausfeld J H, Shelhamer J H, Kaliner M A
Allergic Diseases Section, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, Maryland 20892.
Neuropeptides. 1992 Apr;21(4):231-8. doi: 10.1016/0143-4179(92)90027-t.
The role of neuropeptides in the regulation of macromolecule secretion from human nasal mucosa is incompletely understood. Previous in vitro explant culture studies have demonstrated the effects of neuropeptides on lactoferrin release from serous cells and 3H-glucosamine labeled respiratory glycoconjugate secretion from mucus-containing cells. The generation of a new monoclonal antibody, 7F10, has led to the development of an ELISA for high molecular weight respiratory mucous glycoproteins (MGP). This ELISA was used to measure the ability of sensory, parasympathetic and sympathetic neuropeptides to stimulate MGP release from human nasal mucosal fragments in short term explant culture in vitro. Significant MGP release was stimulated by the sensory neuropeptides gastrin releasing peptide (10 microM GRP: 10.6% +/- 2.4% increase, n = 8, P less than 0.01 vs. control), substance P (1 microM SP: 12.5% +/- 5.4%, n = 11, P less than 0.05), neurokinin A (1 microM NKA: 17.8 +/- 4.3%, n = 6, P less than 0.01), while calcitonin gene related peptide (CGRP) was without effect. Vasoactive intestinal peptide (VIP), a neurotransmitter from parasympathetic nerves, induced significant dose dependent MGP secretion, but had no additive or inhibitory interaction with methacholine-induced secretion. Neuropeptide Y (NPY), present in sympathetic nerves, had no effect on MGP secretion. These observations correlate with the effects of neuropeptides on serous cell lactoferrin secretion, and the presence of specific GRP, SP, and VIP binding sites on human nasal submucosal glands that have been detected by autoradiography. GRP and tachykinins (SP and NKA) from sensory nerves, and VIP released during parasympathetic reflexes may significantly stimulate mucous and serous cell secretion from human nasal mucosa in vivo.
神经肽在调节人鼻黏膜大分子分泌中的作用尚未完全明确。以往的体外组织块培养研究已证实神经肽对浆液细胞乳铁蛋白释放以及含黏液细胞分泌的3H-葡萄糖胺标记的呼吸道糖缀合物的影响。一种新的单克隆抗体7F10的产生,促成了一种用于检测高分子量呼吸道黏液糖蛋白(MGP)的酶联免疫吸附测定(ELISA)的开发。该ELISA用于在体外短期组织块培养中测量感觉、副交感和交感神经肽刺激人鼻黏膜碎片释放MGP的能力。感觉神经肽胃泌素释放肽(10微摩尔GRP:增加10.6%±2.4%,n = 8,与对照组相比P<0.01)、P物质(1微摩尔SP:12.5%±5.4%,n = 11,P<0.05)、神经激肽A(1微摩尔NKA:17.8±4.3%,n = 6,P<0.01)可显著刺激MGP释放,而降钙素基因相关肽(CGRP)则无作用。副交感神经的神经递质血管活性肠肽(VIP)可诱导显著的剂量依赖性MGP分泌,但与乙酰甲胆碱诱导的分泌无相加或抑制性相互作用。存在于交感神经中的神经肽Y(NPY)对MGP分泌无影响。这些观察结果与神经肽对浆液细胞乳铁蛋白分泌的影响以及通过放射自显影检测到的人鼻黏膜下腺上特定的GRP、SP和VIP结合位点的存在相关。感觉神经的GRP和速激肽(SP和NKA)以及副交感反射期间释放的VIP可能在体内显著刺激人鼻黏膜的黏液和浆液细胞分泌。