Usuki J, Horiba K, Chu S C, Moss J, Ferrans V J
Pathology Section, Pulmonary-Critical Care Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892-1518, USA.
Arch Pathol Lab Med. 1998 Oct;122(10):895-902.
Pulmonary lymphangioleiomyomatosis (LAM), a disease of young women, is characterized by proliferation of abnormal smooth muscle cells (LAM cells), which often differ from normal pulmonary smooth muscle cells by frequently having estrogen and progesterone receptors.
To evaluate the relationships among several factors related to proliferation and apoptosis in LAM cells, we employed immunohistochemical methods for the localization of Bcl-2 and Mcl-1 (inhibitors of apoptosis), Bax (a promoter of apoptosis), c-Myc (an apoptosis-related oncoprotein), proliferating cell nuclear antigen (an indicator of mitotic activity), and nick end labeling (to identify apoptotic cells) in lung tissues of 9 patients with LAM.
In all patients, most LAM cells reacted positively for Bax. The LAM cells were positive for both Bcl-2 and estrogen receptor in 5 patients, positive for only Bcl-2 in 1 patient, positive for only estrogen receptor in another patient, and negative for both in 2 patients. More than 50% of the Bcl-2-positive LAM cells were also positive for estrogen receptor. The reaction for c-Myc was positive in all patients. The immunoreactivity for Bcl-2 and Mcl-1, which inhibit apoptosis, was more intense in LAM cells than in normal vascular and bronchial smooth muscle cells. In 6 patients, more than 50% of the LAM cells were positive for proliferating cell nuclear antigen. Apoptosis was infrequent in LAM cells.
Our results suggest that the expression of Bcl-2 in LAM cells may be related to hormonal regulation, and that by decreasing apoptosis, Bcl-2 and related proteins contribute to the imbalance between proliferation and death of LAM cells.
肺淋巴管平滑肌瘤病(LAM)是一种年轻女性疾病,其特征是异常平滑肌细胞(LAM细胞)增殖,这些细胞通常与正常肺平滑肌细胞不同,常含有雌激素和孕激素受体。
为评估与LAM细胞增殖和凋亡相关的几个因素之间的关系,我们采用免疫组化方法对9例LAM患者肺组织中的Bcl-2和Mcl-1(凋亡抑制因子)、Bax(凋亡促进因子)、c-Myc(一种与凋亡相关的癌蛋白)、增殖细胞核抗原(有丝分裂活性指标)进行定位,并采用缺口末端标记法(识别凋亡细胞)。
所有患者中,大多数LAM细胞Bax反应呈阳性。5例患者的LAM细胞Bcl-2和雌激素受体均为阳性,1例患者仅Bcl-2阳性,另1例患者仅雌激素受体阳性,2例患者两者均为阴性。超过50%的Bcl-2阳性LAM细胞雌激素受体也呈阳性。所有患者c-Myc反应均为阳性。抑制凋亡的Bcl-2和Mcl-1在LAM细胞中的免疫反应性比正常血管和支气管平滑肌细胞更强。6例患者中,超过50%的LAM细胞增殖细胞核抗原呈阳性。LAM细胞中凋亡罕见。
我们的结果表明,LAM细胞中Bcl-2的表达可能与激素调节有关,并且通过减少凋亡,Bcl-2及相关蛋白导致LAM细胞增殖与死亡之间的失衡。