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J Exp Med. 1992 Aug 1;176(2):611-6. doi: 10.1084/jem.176.2.611.
2
Human hematopoietic cells and thymic epithelial cells induce tolerance via different mechanisms in the SCID-hu mouse thymus.人类造血细胞和胸腺上皮细胞在SCID-hu小鼠胸腺中通过不同机制诱导免疫耐受。
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3
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B7 expression on thymic medullary epithelium correlates with epithelium-mediated deletion of V beta 5+ thymocytes.胸腺髓质上皮细胞上的B7表达与上皮细胞介导的Vβ5⁺胸腺细胞缺失相关。
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本文引用的文献

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Immunosuppression with cyclosporin A alters the thymic microenvironment.用环孢菌素A进行免疫抑制会改变胸腺微环境。
Clin Exp Immunol. 1989 Nov;78(2):263-70.
2
Biochemical characterization and cellular distribution of a polymorphic, murine cell-surface glycoprotein expressed on lymphoid tissues.在淋巴组织上表达的一种多态性小鼠细胞表面糖蛋白的生化特性及细胞分布
Immunogenetics. 1982 Mar;15(3):299-312. doi: 10.1007/BF00364338.
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Stromal cell types in the developing thymus of the normal and nude mouse embryo.正常和裸鼠胚胎发育中的胸腺基质细胞类型。
Eur J Immunol. 1985 Jul;15(7):675-81. doi: 10.1002/eji.1830150707.
4
Epithelial heterogeneity in the murine thymus: fucose-specific lectins bind medullary epithelial cells.小鼠胸腺中的上皮细胞异质性:岩藻糖特异性凝集素与髓质上皮细胞结合。
J Immunol. 1985 May;134(5):2971-7.
5
Effects of cyclosporine A on T cell development and clonal deletion.环孢素A对T细胞发育和克隆清除的影响。
Science. 1988 Sep 23;241(4873):1655-8. doi: 10.1126/science.241.4873.1655.
6
Normal thymic cortical epithelial cells developmentally regulate the expression of a B-lineage transformation-associated antigen.正常胸腺皮质上皮细胞在发育过程中调节B细胞系转化相关抗原的表达。
Immunogenetics. 1988;27(3):180-6. doi: 10.1007/BF00346584.
7
Total lymphoid irradiation leads to transient depletion of the mouse thymic medulla and persistent abnormalities among medullary stromal cells.全身淋巴组织照射导致小鼠胸腺髓质短暂耗竭以及髓质基质细胞持续异常。
J Immunol. 1988 May 15;140(10):3373-9.
8
Disorganization and restoration of thymic medullary epithelial cells in T cell receptor-negative scid mice: evidence that receptor-bearing lymphocytes influence maturation of the thymic microenvironment.T细胞受体阴性的重度联合免疫缺陷小鼠胸腺髓质上皮细胞的紊乱与恢复:携带受体的淋巴细胞影响胸腺微环境成熟的证据。
Eur J Immunol. 1991 Jul;21(7):1657-61. doi: 10.1002/eji.1830210711.
9
Reentry of T cells to the adult thymus is restricted to activated T cells.T细胞重新进入成年胸腺仅限于活化的T细胞。
J Exp Med. 1991 May 1;173(5):1039-46. doi: 10.1084/jem.173.5.1039.
10
Mature murine B and T cells transferred to SCID mice can survive indefinitely and many maintain a virgin phenotype.转移至重症联合免疫缺陷(SCID)小鼠体内的成熟鼠源B细胞和T细胞能够无限期存活,并且许多细胞保持未激活状态的表型。
J Exp Med. 1991 Sep 1;174(3):717-28. doi: 10.1084/jem.174.3.717.

胸腺髓质中上皮细胞的生长受成熟T细胞的控制。

Growth of epithelial cells in the thymic medulla is under the control of mature T cells.

作者信息

Surh C D, Ernst B, Sprent J

机构信息

Department of Immunology, Scripps Research Institute, La Jolla, California 92037.

出版信息

J Exp Med. 1992 Aug 1;176(2):611-6. doi: 10.1084/jem.176.2.611.

DOI:10.1084/jem.176.2.611
PMID:1500862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2119324/
Abstract

Epithelial cells in the thymic medulla are conspicuous in normal adult mice, but sparse in the early fetal thymus and the thymus of adult T cell-deficient SCID mice. To examine whether growth of medullary epithelial cells (MEC) depends upon local contact with mature T cells, we used the finding that the SCID thymus is unusually permeable to mature T cells entering from the bloodstream. When SCID mice received multiple injections of mature lymph node T cells from birth, the thymus accumulated large numbers of mature TCR+ T cells of resting phenotype, but contained virtually no immature (CD4+8+) cells. The injected T cells localized in the medullary region of the thymus and led to marked regeneration of MEC. These and other data suggest that the growth of MEC is under the control of mature T cells. Placing MEC under T cell control might be a device for regulating the size and integrity of the medulla, especially during the phase of rapid thymic growth. Maintaining the cellular components of the medulla in proper balance could be critical for ensuring efficient self tolerance induction.

摘要

在正常成年小鼠中,胸腺髓质中的上皮细胞很明显,但在早期胎儿胸腺和成年T细胞缺陷的SCID小鼠的胸腺中则很稀疏。为了研究髓质上皮细胞(MEC)的生长是否依赖于与成熟T细胞的局部接触,我们利用了SCID胸腺对从血液中进入的成熟T细胞具有异常通透性这一发现。当SCID小鼠从出生起多次注射成熟淋巴结T细胞时,胸腺积累了大量具有静止表型的成熟TCR+ T细胞,但几乎不包含未成熟(CD4+8+)细胞。注入的T细胞定位于胸腺的髓质区域,并导致MEC显著再生。这些以及其他数据表明,MEC的生长受成熟T细胞的控制。将MEC置于T细胞控制之下可能是一种调节髓质大小和完整性的机制,尤其是在胸腺快速生长阶段。维持髓质细胞成分的适当平衡对于确保有效的自身耐受诱导可能至关重要。