正常骆驼乳腺黏附分子与细胞群的关系

K. T. A. Salem, S. Ramadan, A. M. Alluwaim
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引用次数: 4

摘要

世界范围内对骆驼奶的需求正在增加。乳品工业的新进展使骆驼奶的商业化生产成为可能。骆驼乳腺免疫系统没有详细探讨。本研究旨在鉴定在两个不同生理阶段参与调节骆驼乳腺细胞转运的细胞粘附分子;哺乳期和非哺乳期。探讨健康骆驼肺泡组织、乳腺上淋巴结、Peyer’s斑块、肠系膜淋巴结中CD标志物及黏附分子CD4 +、CD8 +、MAdCAM-1、WC+1 +、CD62L、CD11a/CD18 (LFA-1)、VCAM-1、TCR-、CD44 +、CD20 +的表达和分布。采用免疫过氧化物酶染色原位免疫组化技术检测粘附分子的表达。MAdCAM-1几乎在两个生理阶段的所有组织中都检测到,其中在非哺乳期高表达明显。CD8 + t细胞在乳腺肺泡组织和乳上淋巴结均有表达,在哺乳期表达最高。两期乳腺组织及乳上淋巴结中细胞均可见WC+1 +表达;而非哺乳期表达量较高。尽管CD20 +、CD62L、VCAM-1、TCR- α和CD44 +在抗体所针对的原物种中表达,但检测均失败。CD4 +和CD11a/CD18 (LFA-1)表达均未见明显变化。MAdCAM-1在骆驼乳腺中的密集表达可能表明骆驼乳腺细胞运输与肠道免疫系统(粘膜)密切相关,而不是像牛乳腺那样与外周免疫系统密切相关。WC+1 +的高表达强烈反映了这些细胞亚群在哺乳后期骆驼乳腺防御机制中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adhesion Molecules and the Cellular Population of the Normal Camel (Camelus dromedaries) Mammary Glands
The demand to camel's (Camelus dromedaries) milk is increasing worldwide. The new advances in the dairy industry have made the camel milk production on the commercial level is possible. The camel mammary glands immune system is not explored in detail. This study was conducted to identify the cell adhesion molecules involved in the regulation of the cells trafficking to the camel mammary glands at two different physiological stages; lactation and non- lactating periods. The expression and distribution of CD markers and the adhesion molecules, CD4 + , CD8 + , MAdCAM-1, WC+1 + , CD62L, CD11a/CD18 (LFA-1), VCAM-1, TCR-�� , CD44 + and CD20 + in the alveolar tissues, supramammary lymph nodes, Peyer's patches and mesenteric lymph node of the healthy camels were explored. The expression of the adhesion molecules was determined in situ by immunohistochemical technique using immunoperoxidase staining. MAdCAM-1 was detected in almost all the tissues at the two physiological stages in which high expression was evident in the non-lactating period. CD8 + T-cells were detected in both mammary alveolar tissues and the supramammary lymph nodes, with the highest expression observed in the lactating period. WC+1 + expression on  cells were evident in mammary tissues and supramammary lymph nodes at both stages; however, the expression was higher in the non-lactating period. The detection of CD20 + , CD62L, VCAM-1, TCR-�� , and CD44 + expression failed despite their expression in the original species that the antibodies were raised against. The expression of CD4 + and CD11a/CD18 (LFA-1) were not detected at all. The intensive expression of the MAdCAM-1 in the camel mammary glands could indicates that camel mammary glands cells trafficking is closely linked to the intestinal immune system (mucosal) rather than peripheral as it is well known for the bovine mammary glands. The high expression of WC+1 + strongly reflects the importance of these cells subset in the defense mechanism of the camel mammary glands during the late lactation.
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