Journal of Tuberculosis and Lung Disease ›› 2023, Vol. 4 ›› Issue (5): 397-406.doi: 10.19983/j.issn.2096-8493.20230092
• Review Articles • Previous Articles Next Articles
Received:
2023-08-17
Online:
2023-10-20
Published:
2023-10-16
Contact:
Chen Yan, Email:CLC Number:
Cui Yanan, Chen Yan. Programmed cell death and its research progress in chronic obstructive pulmonary disease[J]. Journal of Tuberculosis and Lung Disease , 2023, 4(5): 397-406. doi: 10.19983/j.issn.2096-8493.20230092
Add to citation manager EndNote|Ris|BibTeX
URL: http://www.jtbld.cn/EN/10.19983/j.issn.2096-8493.20230092
[1] | Pauwels RA, Buist AS, Calverley PM, et al. Global strategy for the diagnosis, management and prevention of chronic obstructive pulmonary disease[EB/OL]. [2023-08-16]. http://www.goldcopd.org/guidelines-global-strategy-for-diagnosis-management.html. |
[2] | World Health Organization. Projections of mortality and causes of death, 2016 and 2060.Geneva:World Health Organization, 2022. |
[3] |
Wang C, Xu J, Yang L, et al. Prevalence and risk factors of chronic obstructive pulmonary disease in china (the china pulmonary health [cph] study): A national cross-sectional study. Lancet, 2018, 391(10131): 1706-1717. doi:10.1016/s0140-6736(18)30841-9.
pmid: 29650248 |
[4] |
Tang D, Kang R, Berghe TV, et al. The molecular machinery of regulated cell death. Cell Res, 2019, 29(5): 347-364. doi:10.1038/s41422-019-0164-5.
pmid: 30948788 |
[5] | Erekat NS. Apoptosis and its Role in Parkinson's Disease//Stoker TB, Greenland JC, editors. Parkinson's Disease: Pathogenesis and Clinical Aspects. Brisbane (AU): Codon Publications, 2018. |
[6] |
Erekat NS. Cerebellar purkinje cells die by apoptosis in the shaker mutant rat. Brain Res, 2017, 1657: 323-332. doi:10.1016/j.brainres.2016.12.025.
pmid: 28040459 |
[7] | Erekat NS. Apoptosis and its therapeutic implications in neurodegenerative diseases. Clin Anat, 2022, 35(1): 65-78. doi:10.1002/ca.23792. |
[8] |
Erekat NS. Programmed cell death in cerebellar purkinje neurons. J Integr Neurosci, 2022, 21(1): 30. doi:10.31083/j.jin2101030.
pmid: 35164466 |
[9] | Wang X, Li F, Liu J, et al. New insights into the mechanism of hepatocyte apoptosis induced by typical organophosphate ester: An integrated in vitro and in silico approach. Ecotoxicol Environ Saf, 2021, 219: 112342. doi:10.1016/j.ecoenv.2021.112342. |
[10] |
Vogeler S, Carboni S, Li X, et al. Phylogenetic analysis of the caspase family in bivalves: Implications for programmed cell death, immune response and development. BMC Genomics, 2021, 22(1): 80. doi:10.1186/s12864-021-07380-0.
pmid: 33494703 |
[11] | Al-Jarrah MD, Erekat NS. Endurance exercise training suppresses parkinson disease-induced overexpression of apoptotic mediators in the heart. Neuro Rehabilitation, 2021, 48(3): 315-320. doi:10.3233/nre-201650. |
[12] |
Tummers B, Green DR. Caspase-8: Regulating life and death. Immunol Rev, 2017, 277(1): 76-89. doi:10.1111/imr.12541.
pmid: 28462525 |
[13] | Mandal R, Barrón JC, Kostova I, et al. Caspase-8: The double-edged sword. Biochim Biophys Acta Rev Cancer, 2020, 1873(2): 188357. doi:10.1016/j.bbcan.2020.188357. |
[14] | Erekat NS. Cerebellar upregulation of cell surface death receptor-mediated apoptotic factors in harmaline-induced tremor: An immunohistochemistry study. J Cell Death, 2018, 11: 1179066018809091. doi:10.1177/1179066018809091. |
[15] |
Ding Y, Wang H, Niu J, et al. Induction of ros overload by alantolactone prompts oxidative DNA damage and apoptosis in colorectal cancer cells. Int J Mol Sci, 2016, 17(4): 558. doi:10.3390/ijms17040558.
pmid: 27089328 |
[16] | Soini T, Pihlajoki M, Kyrönlahti A, et al. Downregulation of transcription factor gata 4 sensitizes human hepatoblastoma cells to doxorubicin-induced apoptosis. Tumour Biol, 2017, 39(3): 1010428317695016. doi:10.1177/1010428317695016. |
[17] | Morris DL, Tjandra N. Inducible fold-switching as a mechanism to fibrillate pro-apoptotic bcl-2 proteins. Biopolymers, 2021, 112(10): e23424. doi:10.1002/bip.23424. |
[18] |
Elena-Real CA, Díaz-Quintana A, González-Arzola K, et al. Cytochrome c speeds up caspase cascade activation by blocking 14-3-3ε-dependent apaf-1 inhibition. Cell Death Dis, 2018, 9(3): 365. doi:10.1038/s41419-018-0408-1.
pmid: 29511177 |
[19] |
Dorstyn L, Akey CW, Kumar S. New insights into apoptosome structure and function. Cell Death Differ, 2018, 25(7): 1194-1208. doi:10.1038/s41418-017-0025-z.
pmid: 29765111 |
[20] |
Erekat NS. Active caspase-3 upregulation is augmented in at-risk cerebellar purkinje cells following inferior olive chemoablation in the shaker mutant rat: An immunofluorescence study. Neurol Res, 2019, 41(3): 234-241. doi:10.1080/01616412.2018.1548792.
pmid: 30462592 |
[21] |
Liu C, Zhang K, Shen H, et al. Necroptosis: A novel manner of cell death, associated with stroke (review). Int J Mol Med, 2018, 41(2): 624-630. doi:10.3892/ijmm.2017.3279.
pmid: 29207014 |
[22] | Dhuriya YK, Sharma D. Necroptosis: A regulated inflammatory mode of cell death. J Neuroinflammation, 2018, 15(1): 199. doi:10.1186/s12974-018-1235-0. |
[23] | Yu Z, Jiang N, Su W, et al. Necroptosis: A novel pathway in neuroinflammation. Front Pharmacol, 2021, 12: 701564. doi:10.3389/fphar.2021.701564. |
[24] | Catalani E, Giovarelli M, Zecchini S, et al. Oxidative stress and autophagy as key targets in melanoma cell fate. Cancers (Basel), 2021, 13(22):5791. doi:10.3390/cancers13225791. |
[25] |
Noda T, Suzuki K, Ohsumi Y. Yeast autophagosomes: De novo formation of a membrane structure. Trends Cell Biol, 2002, 12(5): 231-235. doi:10.1016/s0962-8924(02)02278-x.
pmid: 12062171 |
[26] | Harnett MM, Pineda MA, Latré de Laté P, et al. From christian de duve to yoshinori ohsumi: More to autophagy than just dining at home. Biomed J, 2017, 40(1): 9-22. doi:10.1016/j.bj.2016.12.004. |
[27] |
Strasser A, Vaux DL. Cell death in the origin and treatment of cancer. Mol Cell, 2020, 78(6): 1045-1054. doi:10.1016/j.molcel.2020.05.014.
pmid: 32516599 |
[28] |
Tsujimoto Y, Shimizu S. Another way to die: Autophagic programmed cell death. Cell Death Differ, 2005, 12 Suppl 2: 1528-1534. doi:10.1038/sj.cdd.4401777.
pmid: 16247500 |
[29] |
Denton D, Kumar S. Autophagy-dependent cell death. Cell Death Differ, 2019, 26(4): 605-616. doi:10.1038/s41418-018-0252-y.
pmid: 30568239 |
[30] |
Erekat NS. Autophagy precedes apoptosis among at risk cerebellar purkinje cells in the shaker mutant rat: An ultrastructural study. Ultrastruct Pathol, 2018, 42(2): 162-169. doi:10.1080/01913123.2018.1424744.
pmid: 29419349 |
[31] | Tooze SA, Abada A, Elazar Z. Endocytosis and autophagy: Exploitation or cooperation? Cold Spring Harb Perspect Biol, 2014, 6(5): a018358. doi:10.1101/cshperspect.a018358. |
[32] | Yamahara K, Yasuda M, Kume S, et al. The role of auto-phagy in the pathogenesis of diabetic nephropathy. J Diabetes Res, 2013, 2013: 193757. doi:10.1155/2013/193757. |
[33] | Lystad AH, Simonsen A. Mechanisms and pathophysiological roles of the ATG8 conjugation machinery. Cells, 2019, 8(9):973. doi:10.3390/cells8090973. |
[34] | Wei Y, Liu M, Li X, et al. Origin of the autophagosome membrane in mammals. Biomed Res Int, 2018, 2018: 1012789. doi:10.1155/2018/1012789. |
[35] |
Shin WH, Park JH, Chung KC. The central regulator p62 between ubiquitin proteasome system and autophagy and its role in the mitophagy and parkinson's disease. BMB Rep, 2020, 53(1): 56-63. doi:10.5483/BMBRep.2020.53.1.283.
pmid: 31818366 |
[36] | Herzig S, Shaw RJ. Ampk: Guardian of metabolism and mitochondrial homeostasis. Nat Rev Mol Cell Biol, 2018, 19(2): 121-135. doi:10.1038/nrm.2017.95. |
[37] | Lin SC, Hardie DG. Ampk: Sensing glucose as well as cellular energy status. Cell Metab, 2018, 27(2): 299-313. doi:10.1016/j.cmet.2017.10.009. |
[38] |
Jhanwar-Uniyal M, Wainwright JV, Mohan AL, et al. Diverse signaling mechanisms of mtor complexes: Mtorc1 and mtorc2 in forming a formidable relationship. Adv Biol Regul, 2019, 72: 51-62. doi:10.1016/j.jbior.2019.03.003.
pmid: 31010692 |
[39] | Ribeiro M, López de Figueroa P, Blanco FJ, et al. Insulin decreases autophagy and leads to cartilage degradation. Osteoarthritis Cartilage, 2016, 24(4): 731-739. doi:10.1016/j.joca.2015.10.017. |
[40] | Li D, Ding Z, Du K, et al. Reactive oxygen species as a link between antioxidant pathways and autophagy. Oxid Med Cell Longev, 2021, 2021: 5583215. doi:10.1155/2021/5583215. |
[41] | Ligeon LA, Pena-Francesch M, Vanoaica LD, et al. Oxidation inhibits autophagy protein deconjugation from phagosomes to sustain mhc class ii restricted antigen presentation. Nat Commun, 2021, 12(1): 1508. doi:10.1038/s41467-021-21829-6. |
[42] |
Fink SL, Cookson BT. Apoptosis, pyroptosis, and necrosis: Mechanistic description of dead and dying eukaryotic cells. Infect Immun, 2005, 73(4): 1907-1916. doi:10.1128/iai.73.4.1907-1916.2005.
pmid: 15784530 |
[43] |
Cookson BT, Brennan MA. Pro-inflammatory programmed cell death. Trends Microbiol, 2001, 9(3): 113-114. doi:10.1016/s0966-842x(00)01936-3.
pmid: 11303500 |
[44] | Yu P, Zhang X, Liu N, et al. Pyroptosis: Mechanisms and diseases. Signal Transduct Target Ther, 2021, 6(1): 128. doi:10.1038/s41392-021-00507-5. |
[45] |
Kayagaki N, Wong MT, Stowe IB, et al. Noncanonical inflammasome activation by intracellular lps independent of tlr4. Science, 2013, 341(6151): 1246-1249. doi:10.1126/science.1240248.
pmid: 23887873 |
[46] | Downs KP, Nguyen H, Dorfleutner A, et al. An overview of the non-canonical inflammasome. Mol Aspects Med, 2020, 76: 100924. doi:10.1016/j.mam.2020.100924. |
[47] | Orning P, Weng D, Starheim K, et al. Pathogen blockade of tak 1 triggers caspase-8-dependent cleavage of gasdermin d and cell death. Science, 2018, 362(6418): 1064-1069. doi:10.1126/science.aau2818. |
[48] | Shi J, Zhao Y, Wang K, et al. Cleavage of gsdmd by inflammatory caspases determines pyroptotic cell death. Nature, 2015, 526(7575): 660-665. doi:10.1038/nature15514. |
[49] | Kayagaki N, Stowe IB, Lee BL, et al. Caspase-11 cleaves gasdermin d for non-canonical inflammasome signalling. Nature, 2015, 526(7575): 666-671. doi:10.1038/nature15541. |
[50] | Yang WS, Kim KJ, Gaschler MM, et al. Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis. Proc Natl Acad Sci U S A, 2016, 113(34): E4966-4975. doi:10.1073/pnas.1603244113. |
[51] |
Xie Y, Hou W, Song X, et al. Ferroptosis: Process and function. Cell Death Differ, 2016, 23(3): 369-379. doi:10.1038/cdd.2015.158.
pmid: 26794443 |
[52] | Xu T, Cui J, Xu R, et al. Microplastics induced inflammation and apoptosis via ferroptosis and the nf-κb pathway in carp. Aquat Toxicol, 2023, 262: 106659. doi:10.1016/j.aquatox.2023.106659. |
[53] |
Canli Ö, Alankuş YB, Grootjans S, et al. Glutathione peroxidase 4 prevents necroptosis in mouse erythroid precursors. Blood, 2016, 127(1): 139-148. doi:10.1182/blood-2015-06-654194.
pmid: 26463424 |
[54] |
Kang R, Zeng L, Zhu S, et al. Lipid peroxidation drives gasdermin d-mediated pyroptosis in lethal polymicrobial sepsis. Cell Host Microbe, 2018, 24(1): 97-108. doi:10.1016/j.chom.2018.05.009.
pmid: 29937272 |
[55] | Zheng DW, Lei Q, Zhu JY, et al. Switching apoptosis to ferroptosis: Metal-organic network for high-efficiency anticancer therapy. Nano Lett, 2017, 17(1): 284-291. doi:10.1021/acs.nanolett.6b04060. |
[56] | Hong SH, Lee DH, Lee YS, et al. Molecular crosstalk between ferroptosis and apoptosis: Emerging role of er stress-induced p53-independent puma expression. Oncotarget, 2017, 8(70): 115164-115178. doi:10.18632/oncotarget.23046. |
[57] |
Zille M, Karuppagounder SS, Chen Y, et al. Neuronal death after hemorrhagic stroke in vitro and in vivo shares features of ferroptosis and necroptosis. Stroke, 2017, 48(4): 1033-1043. doi:10.1161/strokeaha.116.015609.
pmid: 28250197 |
[58] |
Li Q, Weiland A, Chen X, et al. Ultrastructural characteristics of neuronal death and white matter injury in mouse brain tissues after intracerebral hemorrhage: Coexistence of ferroptosis, autophagy, and necrosis. Front Neurol, 2018, 9: 581. doi:10.3389/fneur.2018.00581.
pmid: 30065697 |
[59] |
Müller T, Dewitz C, Schmitz J, et al. Necroptosis and ferroptosis are alternative cell death pathways that operate in acute kidney failure. Cell Mol Life Sci, 2017, 74(19): 3631-3645. doi:10.1007/s00018-017-2547-4.
pmid: 28551825 |
[60] | Zhou Y, Liao J, Mei Z, et al. Insight into crosstalk between ferroptosis and necroptosis: Novel therapeutics in ischemic stroke. Oxid Med Cell Longev, 2021, 2021: 9991001. doi:10.1155/2021/9991001. |
[61] |
Zhu P, Hu S, Jin Q, et al. Ripk3 promotes er stress-induced necroptosis in cardiac ir injury: A mechanism involving calcium overload/xo/ros/mptp pathway. Redox Biol, 2018, 16: 157-168. doi:10.1016/j.redox.2018.02.019.
pmid: 29502045 |
[62] |
Lamb HM. Double agents of cell death: Novel emerging functions of apoptotic regulators. Febs J, 2020, 287(13): 2647-2663. doi:10.1111/febs.15308.
pmid: 32239637 |
[63] | Karch J, Kanisicak O, Brody MJ, et al. Necroptosis interfaces with momp and the mptp in mediating cell death. PLoS One, 2015, 10(6): e0130520. doi:10.1371/journal.pone.0130520. |
[64] |
Zhang T, Zhang Y, Cui M, et al. Camkii is a rip3 substrate mediating ischemia- and oxidative stress-induced myocardial necroptosis. Nat Med, 2016, 22(2): 175-182. doi:10.1038/nm.4017.
pmid: 26726877 |
[65] | Kang R, Tang D. Autophagy and ferroptosis-what's the connection? Curr Pathobiol Rep, 2017, 5(2): 153-159. doi:10.1007/s40139-017-0139-5. |
[66] |
Zhou B, Liu J, Kang R, et al. Ferroptosis is a type of autophagy-dependent cell death. Semin Cancer Biol, 2020, 66: 89-100. doi:10.1016/j.semcancer.2019.03.002.
pmid: 30880243 |
[67] | Patil N, Walsh P, Carrabre K, et al. Regionally specific human pre-oligodendrocyte progenitor cells produce both oligodendrocytes and neurons after transplantation in a chronically injured spinal cord rat model after glial scar ablation. J Neurotrauma, 2021, 38(6): 777-788. doi:10.1089/neu.2020.7009. |
[68] | Ma S, Dielschneider RF, Henson ES, et al. Ferroptosis and autophagy induced cell death occur independently after siramesine and lapatinib treatment in breast cancer cells. PLoS One, 2017, 12(8): e0182921. doi:10.1371/journal.pone.0182921. |
[69] |
Hou W, Xie Y, Song X, et al. Autophagy promotes ferroptosis by degradation of ferritin. Autophagy, 2016, 12(8): 1425-1428. doi:10.1080/15548627.2016.1187366.
pmid: 27245739 |
[70] |
Xu R, Yang J, Qian Y, et al. Ferroptosis/pyroptosis dual-inductive combinational anti-cancer therapy achieved by transferrin decorated nanomof. Nanoscale Horiz, 2021, 6(4): 348-356. doi:10.1039/d0nh00674b.
pmid: 33687417 |
[71] | 张凡, 强丽霞, 樊迪, 等. 细胞凋亡和凋亡细胞清除与慢性阻塞性肺疾病. 临床肺科杂志, 2017, 22(4):722-725. doi:10.3969/j.issn.1009-6663.2017.04.041. |
[72] | 石孟瑶, 朱洁, 方莉, 等. 芪白平肺胶囊对copd痰瘀阻肺证大鼠肺血管bax、bcl-2表达的影响. 中医药学报, 2022, 50(4):23-27. doi:10.19664/j.cnki.1002-2392.220078. |
[73] | Chen L, Luo L, Kang N, et al. The protective effect of hbo1 on cigarette smoke extract-induced apoptosis in airway epithelial cells. Int J Chron Obstruct Pulmon Dis, 2020, 15: 15-24. doi:10.2147/copd.S234634. |
[74] | He ZH, Chen P, Chen Y, et al. Comparison between cigarette smoke-induced emphysema and cigarette smoke extract-induced emphysema. Tob Induc Dis, 2015, 13(1): 6. doi:10.1186/s12971-015-0033-z. |
[75] |
Li J, Zong D, Chen Y, et al. Anti-apoptotic effect of the shh signaling pathway in cigarette smoke extract induced mle 12 apoptosis. Tob Induc Dis, 2019, 17: 49. doi:10.18332/tid/109753.
pmid: 31516492 |
[76] | Li T, He X, Luo L, et al. F-box protein fbxw17-mediated proteasomal degradation of protein methyltransferase prmt 6 exaggerates cse-induced lung epithelial inflammation and apoptosis. Front Cell Dev Biol, 2021, 9: 599020. doi:10.3389/fcell.2021.599020. |
[77] | 刘佳丽, 赵卉. 坏死性凋亡在慢性阻塞性肺疾病中的研究进展. 临床肺科杂志, 2023, 28(1):117-120. doi:10.3969/j.issn.1009-6663.2023.01.024. |
[78] |
Xu F, Luo M, He L, et al. Necroptosis contributes to urban particulate matter-induced airway epithelial injury. Cell Physiol Biochem, 2018, 46(2): 699-712. doi:10.1159/000488726.
pmid: 29621753 |
[79] | Wang Y, Wang XK, Wu PP, et al. Necroptosis mediates cigarette smoke-induced inflammatory responses in macrophages. Int J Chron Obstruct Pulmon Dis, 2020, 15: 1093-1101. doi:10.2147/copd.S233506. |
[80] | Mao K, Luo P, Geng W, et al. An integrative transcriptomic and metabolomic study revealed that melatonin plays a protective role in chronic lung inflammation by reducing necroptosis. Front Immunol, 2021, 12: 668002. doi:10.3389/fimmu.2021.668002. |
[81] | Lu Z, Van Eeckhoutte HP, Liu G, et al. Necroptosis signaling promotes inflammation, airway remodeling, and emphysema in chronic obstructive pulmonary disease. Am J Respir Crit Care Med, 2021, 204(6): 667-681. doi:10.1164/rccm.202009-3442OC. |
[82] | Chen D, Gregory AD, Li X, et al. Rip3-dependent necroptosis contributes to the pathogenesis of chronic obstructive pulmonary disease. JCI Insight, 2021, 6(12):e144689. doi:10.1172/jci.insight.144689. |
[83] | Guan K, Li H, Chen H, et al. Tmt-based quantitative proteomics analysis reveals the effect of bovine derived mfg-e8 against oxidative stress on rat 16 cells. Food Funct, 2021, 12(16): 7310-7320. doi:10.1039/d1fo01135a. |
[84] |
Huang X, Tan X, Liang Y, et al. Differential damp release was observed in the sputum of copd, asthma and asthma-copd overlap (aco) patients. Sci Rep, 2019, 9(1): 19241. doi:10.1038/s41598-019-55502-2.
pmid: 31848359 |
[85] | Guo X, Li R, Cui J, et al. Induction of ripk3/mlkl-mediated necroptosis by erigeron breviscapus injection exhibits potent antitumor effect. Front Pharmacol, 2023, 14: 1219362. doi:10.3389/fphar.2023.1219362. |
[86] |
Schenk B, Fulda S. Reactive oxygen species regulate smac mimetic/tnfα-induced necroptotic signaling and cell death. Oncogene, 2015, 34(47): 5796-5806. doi:10.1038/onc.2015.35.
pmid: 25867066 |
[87] | 唐艺玲, 张培蓓, 叶贤伟. Pi3k-akt-mtor通路在慢阻肺发病机制中的研究进展. 中国现代医生, 2021, 59(18):178-183. |
[88] | 金洁, 黄敏轩, 马红映, 等. 线粒体损伤在慢性阻塞性肺疾病发病机制中的研究进展. 中国现代医生, 2023, 61(7):91-95. doi:10.3969/j.issn.1673-9701.2023.07.022. |
[89] | Vij N, Chandramani-Shivalingappa P, Van Westphal C, et al. Cigarette smoke-induced autophagy impairment accelerates lung aging, copd-emphysema exacerbations and pathogenesis. Am J Physiol Cell Physiol, 2018, 314(1): c73-c87. doi:10.1152/ajpcell.00110.2016. |
[90] |
Liu Y, Levine B. Autosis and autophagic cell death: The dark side of autophagy. Cell Death Differ, 2015, 22(3): 367-376. doi:10.1038/cdd.2014.143.
pmid: 25257169 |
[91] |
Tan WSD, Shen HM, Wong WSF. Dysregulated autophagy in copd: A pathogenic process to be deciphered. Pharmacol Res, 2019, 144: 1-7. doi:10.1016/j.phrs.2019.04.005.
pmid: 30953685 |
[92] |
Mercado N, Colley T, Baker JR, et al. Bicaudal d1 impairs autophagosome maturation in chronic obstructive pulmonary disease. FASEB Bioadv, 2019, 1(11): 688-705. doi:10.1096/fba.2018-00055.
pmid: 32123815 |
[93] | Wu YF, Li ZY, Dong LL, et al. Inactivation of mtor promotes autophagy-mediated epithelial injury in particulate matter-induced airway inflammation. Autophagy, 2020, 16(3): 435-450. doi:10.1080/15548627.2019.1628536. |
[94] |
Mizumura K, Cloonan SM, Nakahira K, et al. Mitophagy-dependent necroptosis contributes to the pathogenesis of copd. J Clin Invest, 2014, 124(9): 3987-4003. doi:10.1172/jci74985.
pmid: 25083992 |
[95] | Racanelli AC, Choi AMK, Choi ME. Autophagy in chronic lung disease. Prog Mol Biol Transl Sci, 2020, 172: 135-156. doi:10.1016/bs.pmbts.2020.02.001. |
[96] |
Mercado N, Ito K, Barnes PJ. Accelerated ageing of the lung in copd: New concepts. Thorax, 2015, 70(5): 482-489. doi:10.1136/thoraxjnl-2014-206084.
pmid: 25739910 |
[97] |
Ito S, Araya J, Kurita Y, et al. Park2-mediated mitophagy is involved in regulation of hbec senescence in copd pathogenesis. Autophagy, 2015, 11(3): 547-559. doi:10.1080/15548627.2015.1017190.
pmid: 25714760 |
[98] | 张琳, 王韬, 田新瑞. 细胞焦亡在慢性阻塞性肺疾病中作用机制的研究进展. 临床肺科杂志, 2023, 28(4):600-604. doi:10.3969/j.issn.1009-6663.2023.04.021. |
[99] | Zhang MY, Jiang YX, Yang YC, et al. Cigarette smoke extract induces pyroptosis in human bronchial epithelial cells through the ros/nlrp3/caspase-1 pathway. Life Sci, 2021, 269: 119090. doi:10.1016/j.lfs.2021.119090. |
[100] | Mo R, Zhang J, Chen Y, et al. Nicotine promotes chronic obstructive pulmonary disease via inducing pyroptosis activation in bronchial epithelial cells. Mol Med Rep, 2022, 25(3): doi:10.3892/mmr.2022.12608. |
[101] | Zhang C, Zhu W, Meng Q, et al. Halotherapy relieves chronic obstructive pulmonary disease by alleviating nlrp 3 inflammasome-mediated pyroptosis. Ann Transl Med, 2022, 10(23): 1279. doi:10.21037/atm-22-5632. |
[102] | Franklin BS, Bossaller L, De Nardo D, et al. The adaptor asc has extracellular and ‘prionoid’ activities that propagate inflammation. Nat Immunol, 2014, 15(8): 727-737. doi:10.1038/ni.2913. |
[103] | Mo R, Li J, Chen Y, et al. LncRNA GAS5 promotes pyroptosis in COPD by functioning as a ceRNA to regulate the miR-223-3p/nlrp3 axis. Mol Med Rep, 2022, 26(1):219. doi:10.3892/mmr.2022.12735. |
[104] | Rao Y, Gai X, Xiong J, et al. Transient receptor potential cation channel subfamily v member 4 mediates pyroptosis in chronic obstructive pulmonary disease. Front Physiol, 2021, 12: 783891. doi:10.3389/fphys.2021.783891. |
[105] | Wang L, Chen Q, Yu Q, et al. Trem-1 aggravates chronic obstructive pulmonary disease development via activation nlrp 3 inflammasome-mediated pyroptosis. Inflamm Res, 2021, 70(9): 971-980. doi:10.1007/s00011-021-01490-x. |
[106] | 王莹, 陈亚红. 铁代谢及铁死亡在慢性阻塞性肺疾病中的作用. 生理科学进展, 2022, 53(2):105-110. doi:10.3969/j.issn.0559-7765.2022.02.005. |
[107] | Zhang Z, Fu C, Liu J, et al. Hypermethylation of the nrf2 promoter induces ferroptosis by inhibiting the nrf2-gpx4 axis in copd. Int J Chron Obstruct Pulmon Dis, 2021, 16: 3347-3362. doi:10.2147/copd.S340113. |
[108] |
Yoshida M, Minagawa S, Araya J, et al. Involvement of cigarette smoke-induced epithelial cell ferroptosis in copd pathogenesis. Nat Commun, 2019, 10(1): 3145. doi:10.1038/s41467-019-10991-7.
pmid: 31316058 |
[109] | Park EJ, Park YJ, Lee SJ, et al. Whole cigarette smoke condensates induce ferroptosis in human bronchial epithelial cells. Toxicol Lett, 2019, 303: 55-66. doi:10.1016/j.toxlet.2018.12.007. |
[110] | Wang Y, Liao S, Pan Z, et al. Hydrogen sulfide alleviates particulate matter-induced emphysema and airway inflammation by suppressing ferroptosis. Free Radic Biol Med, 2022, 186: 1-16. doi:10.1016/j.freeradbiomed.2022.04.014. |
[111] | Lian N, Zhang Q, Chen J, et al. The role of ferroptosis in bronchoalveolar epithelial cell injury induced by cigarette smoke extract. Front Physiol, 2021, 12: 751206. doi:10.3389/fphys.2021.751206. |
[112] |
Lin Z, Xu Y, Guan L, et al. Seven ferroptosis-specific expressed genes are considered as potential biomarkers for the diagnosis and treatment of cigarette smoke-induced chronic obstructive pulmonary disease. Ann Transl Med, 2022, 10(6): 331. doi:10.21037/atm-22-1009.
pmid: 35433978 |
[113] | Tang X, Li Z, Yu Z, et al. Effect of curcumin on lung epithelial injury and ferroptosis induced by cigarette smoke. Hum Exp Toxicol, 2021, 40(12_suppl): S753-S762. doi:10.1177/09603271211059497. |
[114] | Liu X, Ma Y, Luo L, et al. Dihydroquercetin suppresses cigarette smoke induced ferroptosis in the pathogenesis of chronic obstructive pulmonary disease by activating nrf2-mediated pathway. Phytomedicine, 2022, 96: 153894. doi:10.1016/j.phymed.2021.153894. |
[115] | Cui Y, Luo L, Zeng Z, et al. Mfg-e8 stabilized by deubiquitinase usp14 suppresses cigarette smoke-induced ferroptosis in bronchial epithelial cells. Cell Death Dis, 2023, 14(1): 2. doi:10.1038/s41419-022-05455-8. |
[1] | Lu Yu, Wang Xiaodong. Research progress of non-drug therapy for chronic obstructive pulmonary disease-related fatigue [J]. Journal of Tuberculosis and Lung Disease, 2023, 4(3): 240-245. |
[2] | Gao Wenwan, Guo Jianqiong, Li Tongxin, Han Mei, Yan Xiaofeng, Yang Song, Tang Shenjie. The interpretation of the key points of the Expert Consensus on Immunotherapy for Tuberculosis (2022 edition) [J]. Journal of Tuberculosis and Lung Disease, 2023, 4(3): 194-197. |
[3] | Fan Mingkuan, Zhang Hui. Interpretation of the Evidence-based Guidelines for Active Screening of Pulmonary Tuberculosis in Chinese Communities [J]. Journal of Tuberculosis and Lung Disease, 2023, 4(1): 1-4. |
[4] | Lou Nannan, Guo Jing, Ma Xiang, Gai Zhongtao. Research progress in pathological mechanism and treatment of cough variant asthma [J]. Journal of Tuberculosis and Lung Disease, 2022, 3(6): 521-525. |
[5] | ZHANG Yan-kun, GUAN Yan, ZHAI Jing-jie, HAN Zhao. Application of anti-neovascular endothelial growth factor therapy in tuberculous chorioretinopathy: a case report and literature review [J]. Journal of Tuberculosis and Lung Disease, 2022, 3(3): 222-226. |
[6] | YANG Yang, LU Shui-hua. Adult-onset mendelian susceptibility to mycobacterial disease: a case report and literature review [J]. Journal of Tuberculosis and Lung Disease, 2020, 1(3): 226-232. |
[7] | Jie ZHANG,Yu-qin LIU,Yu-ze LI,Li-qing HAN,Shu-qin LIU,Hong-ming LI,Yang SUN,Yu-ling QI. Renal tuberculosis as manifestation of autonephrectomy in two cases and literature review [J]. Journal of Tuberculosis and Lung Health, 2018, 7(4): 255-260. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||