Khan Ashraf, Tischler Arthur S, Patwardhan Nilima A, DeLellis Ronald A
Department of Pathology & Surgery, University of Massachusetts Medical School, Worcester, MA, USA.
Endocr Pathol. 2003 Fall;14(3):249-55. doi: 10.1007/s12022-003-0017-z.
Previous studies have established that calcitonin (CT) and the calcitonin generelated peptide (CGRP) are synthesized and stored in subsets of hyperplastic parathyroid cells that also contain chromogranin B (Schmid, KW, et al. Lab Invest 73:90, 1995). The purpose of the current study was to determine whether other generic but variably expressed neuroendocrine markers, i.e., synaptophysin (SYN) and CD57 (Leu7), are also present in normal, hyperplastic, and neoplastic parathyroid tissue and to assess their relationships to the presence of CT.
Immunoperoxidase stains for chromogranin A (CgA), chromogranin B (CgB), SYN, CD57, and CT were performed on 54 hyperplastic, 17 neoplastic (adenoma), and 16 normal parathyroid glands. Sequential sections were stained with antibodies to CgA, CgB, SYN, CD57, and CT using standard avidin-biotin-peroxidase techniques.
CgA was diffusely expressed in all normal, hyperplastic, and neoplastic glands. In hyperplasia, CgB was variably expressed in 6 cases (11%), SYN in 6 (11%), CD57 in 15 (28%), and CT in 8 (15%). In adenomas, CgB was variably expressed in 3 (17%), SYN in 3 (17%), CD57 in 4 (23%), and CT in 4 (23%). All normal glands were negative for CgB, SYN, and CT, while CD57 was variably expressed in 17%. Of the 12 glands that were CT positive, 8 were also positive for CgB, 2 for SYN, and 9 for CD57. Four glands that were strongly and diffusely positive for CT were CgB and SYN negative.
CgB, SYN, and CD57 are markers for subsets of hyperplastic and neoplastic parathyroid glands. CT is also expressed in a significant proportion of hyperplastic and neoplastic parathyroid glands, and may be independent of the presence of CgB, SYN, or DD57. The significance of these findings in relationship to the abnormal calcium metabolism in patients with parathyroid hyperplasia remains to be determined.
先前的研究已证实,降钙素(CT)和降钙素基因相关肽(CGRP)在增生的甲状旁腺细胞亚群中合成并储存,这些细胞亚群中还含有嗜铬粒蛋白B(施密德,KW等人。《实验室研究》73:90,1995)。本研究的目的是确定其他一般但表达可变的神经内分泌标志物,即突触素(SYN)和CD57(Leu7),是否也存在于正常、增生和肿瘤性甲状旁腺组织中,并评估它们与CT存在情况的关系。
对54个增生性、17个肿瘤性(腺瘤)和16个正常甲状旁腺进行嗜铬粒蛋白A(CgA)、嗜铬粒蛋白B(CgB)、SYN、CD57和CT的免疫过氧化物酶染色。连续切片使用标准抗生物素蛋白-生物素-过氧化物酶技术,用抗CgA、CgB、SYN、CD57和CT的抗体进行染色。
CgA在所有正常、增生和肿瘤性腺中均呈弥漫性表达。在增生组织中,CgB在6例(11%)中表达可变,SYN在6例(11%)中表达可变,CD57在15例(28%)中表达可变,CT在8例(15%)中表达可变。在腺瘤中,CgB在3例(17%)中表达可变,SYN在3例(17%)中表达可变,CD57在4例(23%)中表达可变,CT在4例(23%)中表达可变。所有正常腺体的CgB、SYN和CT均为阴性,而CD57在17%中表达可变。在12个CT阳性的腺体中,8个CgB也呈阳性,2个SYN呈阳性,9个CD57呈阳性。4个CT呈强弥漫性阳性的腺体CgB和SYN为阴性。
CgB、SYN和CD57是增生性和肿瘤性甲状旁腺亚群的标志物。CT在相当比例的增生性和肿瘤性甲状旁腺中也有表达,并且可能独立于CgB、SYN或DD57的存在。这些发现与甲状旁腺增生患者钙代谢异常的关系的意义尚待确定。