Neiman P E, Thomas S J, Loring G
Fred Hutchinson Cancer Research Center, University of Washington, Seattle 98104.
Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5857-61. doi: 10.1073/pnas.88.13.5857.
The lymphoid cells of embryonic bursal follicles are engaged in rapid growth and preimmune diversification of immunoglobulin genes. Disruption of follicular architecture by mechanical dispersion of these cells in short-term tissue culture was accompanied by continued cell division and extensive cell death by apoptosis. Apoptosis was suppressed in parallel cultures of intact follicles. gamma Radiation also triggered extensive apoptosis in embryonic bursal follicles within a few hours. Preneoplastic bursal stem cell populations induced by a v-myc oncogene were hypersensitive to induction of apoptosis by follicular dispersion and radiation. In contrast, tumor progression in v-myc- and v-rel-initiated bursal neoplasms was accompanied by development of resistance to induction of apoptosis. A programmed cell death pathway can be activated during normal B-cell development in the bursa, and alterations in the expression of this pathway accompany neoplastic change in this system.
胚胎法氏囊滤泡的淋巴细胞参与免疫球蛋白基因的快速生长和免疫前多样化。在短期组织培养中,通过机械分散这些细胞破坏滤泡结构,伴随着细胞持续分裂和广泛的细胞凋亡死亡。在完整滤泡的平行培养物中,细胞凋亡受到抑制。γ辐射也在数小时内引发胚胎法氏囊滤泡广泛的细胞凋亡。由v-myc癌基因诱导的肿瘤前法氏囊干细胞群体对滤泡分散和辐射诱导的细胞凋亡高度敏感。相比之下,v-myc和v-rel引发的法氏囊肿瘤的肿瘤进展伴随着对细胞凋亡诱导的抗性发展。在法氏囊中正常B细胞发育过程中,程序性细胞死亡途径可被激活,并且该途径表达的改变伴随着该系统中的肿瘤性变化。