Lotem J, Sachs L
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12507-12. doi: 10.1073/pnas.93.22.12507.
Apoptosis induced in myeloid leukemic cells by wild-type p53 was suppressed by different cleavage-site directed protease inhibitors, which inhibit interleukin-1 beta-converting enzyme-like, granzyme B and cathepsins B and L proteases. Apoptosis was also suppressed by the serine and cysteine protease inhibitor N-tosyl-L-phenylalanine chloromethylketone (TPCK) [corrected], but not by other serine or cysteine protease inhibitors including N alpha-p-tosyl-L-lysine chloromethylketone (TLCK), E64, pepstatin A, or chymostatin. Protease inhibitors suppressed induction of apoptosis by gamma-irradiation and cycloheximide but not by doxorubicin, vincristine, or withdrawal of interleukin 3 from interleukin 3-dependent 32D non-malignant myeloid cells. Induction of apoptosis in normal thymocytes by gamma-irradiation or dexamethasone was also suppressed by the cleavage-site directed protease inhibitors, but in contrast to the myeloid leukemic cells apoptosis in thymocytes was suppressed by TLCK but not by TPCK. The results indicate that (i) inhibitors of interleukin-1 beta-converting enzyme-like proteases and some other protease inhibitors suppressed induction of apoptosis by wild-type p53 and certain p53-independent pathways of apoptosis; (ii) the protease inhibitors together with the cytokines interleukin 6 and interferon-gamma or the antioxidant butylated hydroxyanisole gave a cooperative protection against apoptosis; (iii) these protease inhibitors did not suppress induction of apoptosis by some cytotoxic agents or by viability-factor withdrawal from 32D cells, whereas these pathways of apoptosis were suppressed by cytokines; (iv) there are cell type differences in the proteases involved in apoptosis; and (v) there are multiple pathways leading to apoptosis that can be selectively induced and suppressed by different agents.
野生型p53诱导的髓系白血病细胞凋亡受到不同切割位点定向蛋白酶抑制剂的抑制,这些抑制剂可抑制白细胞介素-1β转化酶样、颗粒酶B以及组织蛋白酶B和L蛋白酶。丝氨酸和半胱氨酸蛋白酶抑制剂N-对甲苯磺酰-L-苯丙氨酸氯甲基酮(TPCK)[已修正]也可抑制凋亡,但其他丝氨酸或半胱氨酸蛋白酶抑制剂,包括N-α-对甲苯磺酰-L-赖氨酸氯甲基酮(TLCK)、E64、胃蛋白酶抑制剂A或抑肽酶则不能。蛋白酶抑制剂可抑制γ射线照射和环己酰亚胺诱导的凋亡,但不能抑制阿霉素、长春新碱诱导的凋亡,也不能抑制从依赖白细胞介素3的32D非恶性髓系细胞中撤除白细胞介素3诱导的凋亡。γ射线照射或地塞米松诱导的正常胸腺细胞凋亡也受到切割位点定向蛋白酶抑制剂的抑制,但与髓系白血病细胞不同的是,胸腺细胞凋亡受到TLCK抑制,而不受TPCK抑制。结果表明:(i)白细胞介素-1β转化酶样蛋白酶抑制剂和其他一些蛋白酶抑制剂可抑制野生型p53诱导的凋亡以及某些不依赖p53的凋亡途径;(ii)蛋白酶抑制剂与细胞因子白细胞介素6和干扰素-γ或抗氧化剂丁基羟基茴香醚协同保护细胞免受凋亡;(iii)这些蛋白酶抑制剂不能抑制某些细胞毒性药物诱导的凋亡或从32D细胞中撤除生存因子诱导的凋亡,而这些凋亡途径可被细胞因子抑制;(iv)参与凋亡的蛋白酶存在细胞类型差异;(v)存在多种导致凋亡的途径,可被不同药物选择性诱导和抑制。