Szewczuk M R, DeKruyff R H, Goidl E A, Weksler M E, Siskind G W
Eur J Immunol. 1980 Dec;10(12):918-23. doi: 10.1002/eji.1830101206.
The role of thymus cells in mediating a step in the ontogeny of the capacity of the B cell population to produce a heterogeneous, high-affinity, primary, plaque-forming cell (PFC) response was further investigated. It was shown that the thymus acquires the capacity to facilitate this step in B cell differentiation between 3 and 4 weeks of age in C57BL/6 mice. This corresponds to the age at which te splenic B cell population of these mice naturally acquires the capacity to produce high-affinity PFC. The differentiation of the B cell population. It was further shown that regulates this step in the cells to facilitate the maturation of B cell population. It was further shown that the ability of thymus cells to facilitate the maturation of the B cell population decreases with age and is already markedly reduced in 30-week-old, long-lived, C57BL/6 mice. A qualitative or quantitative decrease in thymic function may thus be responsible for age-related changes in the function of the B cell population.
进一步研究了胸腺细胞在介导B细胞群体产生异质性、高亲和力、原发性斑块形成细胞(PFC)反应能力个体发育过程中一个步骤的作用。结果表明,在C57BL/6小鼠中,胸腺在3至4周龄时获得促进B细胞分化这一步骤的能力。这与这些小鼠脾脏B细胞群体自然获得产生高亲和力PFC能力的年龄相对应。B细胞群体的分化。进一步表明,调节细胞中的这一步骤以促进B细胞群体的成熟。进一步表明,胸腺细胞促进B细胞群体成熟的能力随年龄下降,在30周龄的长寿C57BL/6小鼠中已明显降低。因此,胸腺功能的定性或定量下降可能是B细胞群体功能与年龄相关变化的原因。