Sannes P L, Burch K K, Khosla J
Department of Anatomy, Physiological Sciences, and Radiology, North Carolina State University, College of Veterinary Medicine, Raleigh 27606.
Am J Respir Cell Mol Biol. 1992 Aug;7(2):230-7. doi: 10.1165/ajrcmb/7.2.230.
Histologic preparations of lungs form 1-, 5-, 10-, 18-, and 25-day-old rats and adult rats were probed immunohistochemically with specific antibodies for the distribution of epidermal growth factor (EGF), acidic fibroblast growth factor (aFGF), and basic fibroblast growth factor (bFGF). Immunoperoxidase staining of sections of adult rat lungs with a rabbit polyclonal antibody to bovine EGF was strong in ciliated cells of airways and mast cells, nonciliated cells of bronchioles, smooth muscle, type II cells of alveoli, and interstitial and epithelial cells of alveolar septal regions. Developing postnatal lungs had moderate and somewhat diffuse immunoreactivity in all epithelial cells, and more intense staining in vascular smooth muscle. Immunoperoxidase staining of adult rat lungs with a rabbit polyclonal antibody against bovine aFGF was distributed in identical fashion to EGF, with the exception of mast cells which were not reactive. These same sights were localized using an immunoperoxidase sequence with a rabbit polyclonal antibody to the leu 60-leu 98 fragment of aFGF (aFGFfr) with less background. In postnatal developing lungs, immunoreactivity with aFGF and aFGFfr preparations was diffuse and moderately intense in epithelial cells and vascular smooth muscle. Immunoperoxidase staining of adult rat lung sections with a monoclonal antibody to bovine bFGF was strong in hyaluronidase-digested preparations. Reactivity was principally confined to alveolar and vascular basement membrane regions and external laminae of smooth muscle. In early postnatal development, immunoreactivity for bFGF was found in basement membranes beneath developing epithelium and the endothelium of vessel wall intima and in the adventitia, with reactivity increasing with advancing age.(ABSTRACT TRUNCATED AT 250 WORDS)
用针对表皮生长因子(EGF)、酸性成纤维细胞生长因子(aFGF)和碱性成纤维细胞生长因子(bFGF)分布的特异性抗体,对1日龄、5日龄、10日龄、18日龄、25日龄大鼠及成年大鼠的肺组织学标本进行免疫组织化学检测。用兔抗牛EGF多克隆抗体对成年大鼠肺切片进行免疫过氧化物酶染色,在气道纤毛细胞和肥大细胞、细支气管的非纤毛细胞、平滑肌、肺泡Ⅱ型细胞以及肺泡间隔区域的间质和上皮细胞中染色较强。出生后发育中的肺在所有上皮细胞中有中度且有点弥散的免疫反应性,在血管平滑肌中染色更强。用兔抗牛aFGF多克隆抗体对成年大鼠肺进行免疫过氧化物酶染色,其分布方式与EGF相同,但肥大细胞无反应。使用针对aFGF的leu 60 - leu 98片段(aFGFfr)的兔多克隆抗体的免疫过氧化物酶序列定位相同部位,背景较少。在出生后发育的肺中,aFGF和aFGFfr制剂的免疫反应性在上皮细胞和血管平滑肌中是弥散且中度强烈的。用抗牛bFGF单克隆抗体对成年大鼠肺切片进行免疫过氧化物酶染色,在透明质酸酶消化的制剂中染色较强。反应主要局限于肺泡和血管基底膜区域以及平滑肌的外板。在出生后早期发育中,bFGF的免疫反应性在发育中的上皮下方的基底膜、血管壁内膜的内皮和外膜中发现,且随着年龄增长反应性增加。(摘要截短于250字)