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人淋巴结、扁桃体切片及牙周病中淋巴细胞亚群的酶分化

Enzyme differentiation of lymphocyte subpopulations in sections of human lymph nodes, tonsils and periodontal disease.

作者信息

Seymour G J, Dockrell H M, Greenspan J S

出版信息

Clin Exp Immunol. 1978 Apr;32(1):169-78.

PMID:307463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1541303/
Abstract

Five enzymes have been studied to differentiate between T and B lymphocytes in sections of human lymph nodes, tonsils and chronic inflammatory periodontal disease. The presence of acid phosphatase, beta-glucuronidase N-acetyl-beta-glucosaminidase, non-specific esterase and fluoride-resistant esterase activity was determined histochemically. The results indicate that cells in the B area of both lymph nodes and tonsils are negative for enzyme activity, while those in the T area show a single intense granule of activity. These enzymes were unable to differentiate between T blasts, B blasts and plasma cells in the sections studied. The majority of the lymphoid cells in the lesions of chronic inflammatory periodontal disease are enzyme-negative and probably of B-cell origin.

摘要

为区分人类淋巴结、扁桃体及慢性炎症性牙周病切片中的T淋巴细胞和B淋巴细胞,对五种酶进行了研究。通过组织化学方法测定了酸性磷酸酶、β-葡萄糖醛酸酶、N-乙酰-β-氨基葡萄糖苷酶、非特异性酯酶和耐氟酯酶活性的存在情况。结果表明,淋巴结和扁桃体B区的细胞酶活性均为阴性,而T区的细胞则显示单个强烈的活性颗粒。在所研究的切片中,这些酶无法区分T母细胞、B母细胞和浆细胞。慢性炎症性牙周病病变中的大多数淋巴细胞酶呈阴性,可能起源于B细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/a734c1915ad5/clinexpimmunol00224-0182-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/266dd7b22f21/clinexpimmunol00224-0180-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/ea0a7fb8357a/clinexpimmunol00224-0180-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/3fa3269bff9f/clinexpimmunol00224-0178-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/00065b0b72fc/clinexpimmunol00224-0179-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/f932a96b25c0/clinexpimmunol00224-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/fc2875259732/clinexpimmunol00224-0181-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/547c25d5b4d0/clinexpimmunol00224-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/63e06bd4596b/clinexpimmunol00224-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/a734c1915ad5/clinexpimmunol00224-0182-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/266dd7b22f21/clinexpimmunol00224-0180-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/ea0a7fb8357a/clinexpimmunol00224-0180-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/3fa3269bff9f/clinexpimmunol00224-0178-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/00065b0b72fc/clinexpimmunol00224-0179-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/f932a96b25c0/clinexpimmunol00224-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/fc2875259732/clinexpimmunol00224-0181-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/547c25d5b4d0/clinexpimmunol00224-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/63e06bd4596b/clinexpimmunol00224-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a72/1541303/a734c1915ad5/clinexpimmunol00224-0182-c.jpg

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