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中华重症医学电子杂志 ›› 2022, Vol. 08 ›› Issue (02) : 167 -172. doi: 10.3877/cma.j.issn.2096-1537.2022.02.013

综述

肺表面活性蛋白-D功能及其在肺部常见疾病中的研究进展
刘娟丽1, 马四清2,(), 陈强2   
  1. 1. 810007 西宁,青海省人民医院重症医学科;810001 西宁,青海大学高原医学研究中心
    2. 810007 西宁,青海省人民医院重症医学科
  • 收稿日期:2022-02-16 出版日期:2022-07-04
  • 通信作者: 马四清
  • 基金资助:
    国家自然科学基金项目(81860351); 青海省高原重症医学重点实验室项目(2020-81); 青海省高原医学应用基础重点实验室(青海-犹他高原医学联合重点实验室)项目(2022-ZJ-Y15)

Research progress on the function of surfactant protein -D and its role in the common lung diseases

Juanli Liu1, Siqing Ma2,(), Qiang Chen2   

  1. 1. Department of Critical Care Medicine, Qinghai Provincial People′s Hospital, Xining 810007, China; Plateau Medical Center of Qinghai University, Xining 810001, China
    2. Department of Critical Care Medicine, Qinghai Provincial People′s Hospital, Xining 810007, China
  • Received:2022-02-16 Published:2022-07-04
  • Corresponding author: Siqing Ma
引用本文:

刘娟丽, 马四清, 陈强. 肺表面活性蛋白-D功能及其在肺部常见疾病中的研究进展[J]. 中华重症医学电子杂志, 2022, 08(02): 167-172.

Juanli Liu, Siqing Ma, Qiang Chen. Research progress on the function of surfactant protein -D and its role in the common lung diseases[J]. Chinese Journal of Critical Care & Intensive Care Medicine(Electronic Edition), 2022, 08(02): 167-172.

肺表面活性蛋白-D(SP-D)是凝集素家族糖蛋白,主要在肺部的肺泡Ⅱ型上皮细胞和无纤毛细支气管上皮细胞合成和分泌,储存在Clara细胞的分泌颗粒中。SP-D是表面结合蛋白之一,也是组成肺表面活性系统的一部分。SP-D除了有助于肺泡空间内表面活性剂池稳态外,还具有宿主防御和免疫调节功能。本文通过对近年来SP-D在肺部常见疾病中的部分相关研究进行总结,为众多肺部疾病,特别是肺部炎症性疾病潜在的治疗提供重要的方法理论基础。

Lung surfactant protein D (SP-D) is a glycoprotein of the lectin family. In lungs it is synthesized and secreted mainly in the alveolar type Ⅱ epithelial cells and non-ciliated bronchiole epithelial cells, and are stored in secretory granules of Clara cells. SP-D is one of the surfactant binding proteins and is also a part of the pulmonary surfactant system. In addition to contributing to the homeostasis of surfactant pools in alveolar space, SP-D also exhibits functions of host defense and immunoregulation. This paper summarizes some relevant studies on SP-D in acute lung diseases in recent years, providing important theoretical basis for the potential treatment of many lung diseases, especially in inflammatory lung diseases.

1
Chen D, Fang F, Yang Y, et al. Brahma-related gene 1 (Brg1) epigenetically regulates CAM activation during hypoxic pulmonary hypertension [J]. Cardiovasc Res, 2013, 100(3): 363-373.
2
Banerjee M, Saxena M. Interleukin-1 (IL-1) family of cytokines: role in type 2 diabetes [J]. Clin Chim Acta, 2012, 413(15-16): 1163-1170.
3
高钰琪, 黄缄. 炎症反应与高原病 [J]. 第三军医大学学报, 2016, 38(3): 215-219.
4
Persson A, Rust K, Chang D, et al. CP4: a pneumocyte-derived collagenous surfactant-associated protein. Evidence for heterogeneity of collagenous surfactant proteins [J]. Biochemistry, 1988, 27(23): 8576-8584.
5
Miyamura K, Malhotra R. Hoppe HJ, et al. Surfactant proteins A (SP-A) and D (SP-D): levels in human amniotic fluid and localization in the fetal membranes [J]. Biochim Biophys Acta, 1994, 1210(3): 303-307.
6
Stahlman MT, Gray ME, Hull WM, et al. Immunolocalization of surfactant protein-D (SP-D) in human fetal, newborn, and adult tissues [J]. J Histochem Cytochem, 2002, 50(5): 651-660.
7
Sorensen GL. Surfactant Protein D in Respiratory and Non-Respiratory Diseases [J]. Front Med (Lausanne), 2018, 5: 18.
8
Vieira F, Kung JW, Bhatti F. Structure, genetics and function of the pulmonary associated surfactant proteins A and D: The extra-pulmonary role of these C type lectins [J]. Ann Anat, 2017, 211: 184-201.
9
Crouch E, Parghi D, Kuan SF, et al. Surfactant protein D: subcellular localization in nonciliated bronchiolar epithelial cells [J]. Am J Physiol, 1992, 263(1): 60-66.
10
Madsen J, Kliem A, Tornoe I, et al. Localization of lung surfactant protein D on mucosal surfaces in human tissues [J]. J Immunol, 2000, 164(11): 5866-5870.
11
Kishore U, Greenhough TJ, Waters P, et al. Surfactant proteins SP-A and SP-D: structure, function and receptors [J]. Mol Immunol, 2006, 43(9): 1293-1315.
12
Crouch E, Persson A, Chang D. Accumulation of surfactant protein D in human pulmonary alveolar proteinosis [J]. Am J Pathol, 1993, 142(1): 241-248.
13
Crouch EC. Surfactant protein-D and pulmonary host defense [J]. Respir Res, 2000, 1(2): 93-108.
14
Atochina-Vasserman EN. S-nitrosylation of surfactant protein D as a modulator of pulmonary inflammation [J]. Biochim Biophys Acta, 2012, 1820(6): 763-769.
15
Hartshorn KL, White MR, Tecle T, et al. Reduced influenza viral neutralizing activity of natural human trimers of surfactant protein D [J]. Respir Res, 2007, 8(1): 9.
16
Crouch EC, Persson A, Griffin GL, et al. Interactions of pulmonary surfactant protein D (SP-D) with human blood leukocytes [J]. Am J Respir Cell Mol Biol, 1995, 12(4): 410-415.
17
Tino MJ, Wright JR. Surfactant proteins A and D specifically stimulate directed actin-based responses in alveolar macrophages [J]. Am J Physiol, 1999, 276(1): 164-174.
18
Kuan SF, Persson A, Parghi D, et al. Lectin-mediated interactions of surfactant protein D with alveolar macrophages [J]. Am J Respir Cell Mol Biol, 1994, 10(4): 430-406.
19
Ferguson JS, Voelker DR, McCormack FX, et al. Surfactant protein D binds to Mycobacterium tuberculosis bacilli and lipoarabinomannan via carbohydrate-lectin interactions resulting in reduced phagocytosis of the bacteria by macrophages [J]. J Immunol, 1999, 163(1): 312-321.
20
van Rozendaal BA, van de Lest CH, van Eijk M, et al. Aerosolized endotoxin is immediately bound by pulmonary surfactant protein D in vivo [J]. Biochim Biophys Acta, 1999, 1454(3): 261-269.
21
Pikaar JC, Voorhout WF, van Golde LM, et al. Opsonic activities of surfactant proteins A and D in phagocytosis of gram-negative bacteria by alveolar macrophages [J]. J Infect Dis, 1995, 172(2): 481-489.
22
O'Riordan DM, Standing JE, Kwon KY, et al. Surfactant protein D interacts with Pneumocystis carinii and mediates organism adherence to alveolar macrophages [J]. J Clin Invest, 1995, 95(6): 2699-2710.
23
Fearon DT, Locksley RM. The instructive role of innate immunity in the acquired immune response [J]. Science, 1996, 272(5258): 50-53.
24
Brinker KG, Martin E, Borron P, et al. Surfactant protein D enhances bacterial antigen presentation by bone marrow-derived dendritic cells [J]. Am J Physiol Lung Cell Mol Physiol, 2001, 281(6): 1453-1463.
25
Borron PJ, Crouch EC, Lewis JF, et al. Recombinant rat surfactant-associated protein D inhibits human T lymphocyte proliferation and IL-2 production [J]. J Immunol, 1998, 161(9): 4599-4603.
26
Wang JY, Shieh CC, You PF, et al. Inhibitory effect of pulmonary surfactant proteins A and D on allergen-induced lymphocyte proliferation and histamine release in children with asthma [J]. Am J Respir Crit Care Med, 1998, 158(2): 510-518.
27
Kingma PS, Whitsett JA. In defense of the lung: surfactant protein A and surfactant protein D [J]. Curr Opin Pharmacol, 2006, 6(3): 277-283.
28
LeVine AM, Elliott J, Whitsett JA, et al. Surfactant protein-d enhances phagocytosis and pulmonary clearance of respiratory syncytial virus [J]. Am J Respir Cell Mol Biol, 2004, 31(2): 193-199.
29
Ikegami M, Carter K, Bishop K, et al. Intratracheal recombinant surfactant protein d prevents endotoxin shock in the newborn preterm lamb [J]. Am J Respir Crit Care Med, 2006, 173(12): 1342-1347.
30
Ikegami M, Scoville EA, Grant S, et al. Surfactant protein-D and surfactant inhibit endotoxin-induced pulmonary inflammation [J]. Chest, 2007, 132(5): 1447-1454.
31
Sato A, Whitsett JA, Scheule RK, et al. Surfactant protein-d inhibits lung inflammation caused by ventilation in premature newborn lambs [J]. Am J Respir Crit Care Med, 2010, 181(10): 1098-1105.
32
King BA, Kingma PS. Surfactant protein D deficiency increases lung injury during endotoxemia [J]. Am J Respir Cell Mol Biol, 2011, 44(5): 709-715.
33
Arroyo R, Khan MA, Echaide M, et al. SP-D attenuates LPS-induced formation of human neutrophil extracellular traps (NETs), protecting pulmonary surfactant inactivation by NETs [J]. Commun Biol, 2019, 2: 470.
34
LeVine AM, Whitsett JA, Gwozdz JA, et al. Distinct effects of surfactant protein A or D deficiency during bacterial infection on the lung [J]. J Immunol, 2000, 165(7): 3934-3940.
35
张冬青, 王胜云, 刘梅, 等. 脓毒症性ARDS大鼠模型SP蛋白的变化及其干预措施的实验研究 [J]. 实用心脑肺血管病杂志, 2016, 24(1): 237-238.
36
Savill J. Apoptosis in resolution of inflammation [J]. J Leukoc Biol, 1997, 61(4): 375-380.
37
Fadok VA, Bratton DL, Henson PM. Phagocyte receptors for apoptotic cells: recognition, uptake, and consequences [J]. J Clin Invest, 2001, 108(7): 957-962.
38
Fadok VA, Bratton DL, Guthrie L, et al. Differential effects of apoptotic versus lysed cells on macrophage production of cytokines: role of proteases [J]. J Immunol, 2001, 166(11): 6847-6854.
39
Clark H, Palaniyar N, Strong P, et al. Surfactant protein D reduces alveolar macrophage apoptosis in vivo [J]. J Immunol, 2002, 169(6): 2892-2899.
40
Strong P, Reid KB, Clark H. Intranasal delivery of a truncated recombinant human SP-D is effective at down-regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus [J]. Clin Exp Immunol, 2002, 130(1): 19-24.
41
Wright JR. Immunoregulatory functions of surfactant proteins [J]. Nat Rev Immunol, 2005, 5(1): 58-68.
42
Ohya M, Nishitani C, Sano H, et al. Human pulmonary surfactant protein D binds the extracellular domains of Toll-like receptors 2 and 4 through the carbohydrate recognition domain by a mechanism different from its binding to phosphatidylinositol and lipopolysaccharide [J]. Biochemistry, 2006, 45(28): 8657-8664.
43
Yamazoe M, Nishitani C, Takahashi M, et al. Pulmonary surfactant protein D inhibits lipopolysaccharide (LPS)-induced inflammatory cell responses by altering LPS binding to its receptors [J]. J Biol Chem, 2008, 283(51): 35878-35888.
44
Gardai SJ, Xiao YQ, Dickinson M, et al. By binding SIRP alpha or calreticulin/CD91, lung collectins act as dual function surveillance molecules to suppress or enhance inflammation [J]. Cell, 2003, 115(1): 13-23.
45
Bridges JP, Davis HW, Damodarasamy M, et al. Pulmonary surfactant proteins A and D are potent endogenous inhibitors of lipid peroxidation and oxidative cellular injury [J]. J Biol Chem, 2000, 275(49): 38848-38855.
46
Ferguson JS, Voelker DR, McCormack FX, et al. Surfactant protein D binds to Mycobacterium tuberculosis bacilli and lipoarabinomannan via carbohydrate-lectin interactions resulting in reduced phagocytosis of the bacteria by macrophages [J]. J Immunol, 1999, 163(1): 312-321.
47
Zhu N, Zhang D, Wang W, et al. A Novel Coronavirus from Patients with Pneumonia in China, 2019 [J]. N Engl J Med, 2020, 382(8): 727-733.
48
Walls AC, Park YJ, Tortorici MA, et al. Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein [J]. Cell, 2020, 181(2): 281-292.
49
Hoffmann M, Kleine-Weber H, Schroeder S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor [J]. Cell, 2020, 181(2): 271-280.
50
Shang J, Ye G, Shi K, et al. Structural basis of receptor recognition by SARS-CoV-2 [J]. Nature, 2020, 581(7807): 221-224.
51
Wan Y, Shang J, Graham R, et al. Receptor recognition by the novel coronavirus from Wuhan: an analysis based on decade-long structural studies of SARS coronavirus [J]. J Virol, 2020, 94(7): 120-127.
52
Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study [J]. Lancet, 2020, 395(10223): 507-513.
53
Hartshorn K, Chang D, Rust K, et al. Interactions of recombinant human pulmonary surfactant protein D and SP-D multimers with influenza A [J]. Am J Physiol, 1996, 271(5): 753-762.
54
Arroyo R, Grant SN, Colombo M, et al. Full-length recombinant hSP-D binds and inhibits SARS-CoV-2 [J]. Biomolecules, 2021, 11(8):1114.
55
Honda Y, Kuroki Y, Matsuura E, et al. Pulmonary surfactant protein D in sera and bronchoalveolar lavage fluids [J]. Am J Respir Crit Care Med, 1995, 152(6): 1860-1866.
56
Hermans C, Bernard A. Lung epithelium-specific proteins: characteristics and potential applications as markers [J]. Am J Respir Crit Care Med, 1999, 159(2): 646-678.
57
Winkler C, Atochina-Vasserman EN, Holz O, et al. Comprehensive characterisation of pulmonary and serum surfactant protein D in COPD [J]. Respir Res, 2011, 12: 29.
58
Madan T, Biswas B, Varghese PM, et al. A recombinant fragment of human surfactant protein D binds spike protein and inhibits infectivity and replication of SARS-CoV-2 in clinical samples [J]. Am J Respir Cell Mol Biol, 2021, 65(1): 41-53.
59
Arroyo R, Martin-Gonzalez A, Echaide M, et al. Supramolecular Assembly of Human Pulmonary Surfactant Protein SP-D [J]. J Mol Biol, 2018, 430(10): 1495-1509.
60
Arroyo R, Echaide M, Wilmanowski R, et al. Structure and activity of human surfactant protein D from different natural sources [J]. Am J Physiol Lung Cell Mol Physiol, 2020, 319(1): 148-158.
61
Tong M, Xiong Y, Zhu C, et al. Serum surfactant protein D in COVID-19 is elevated and correlated with disease severity [J]. BMC Infect Dis, 2021, 21(1): 737.
62
Cheng IW, Ware LB, Greene KE, et al. Prognostic value of surfactant proteins A and D in patients with acute lung injury [J]. Crit Care Med, 2003, 31(1): 20-27.
63
Johansson J, Curstedt T, Robertson B. The proteins of the surfactant system [J]. Eur Respir J, 1994, 7(2): 372-391.
64
Okada T, Lee BW, Ogami A, et al. Inhalation of titanium dioxide (P25) nanoparticles to rats and changes in surfactant protein (SP-D) levels in bronchoalveolar lavage fluid and serum [J]. Nanotoxicology, 2019, 13(10): 1396-1408.
65
Park J, Pabon M, Choi AMK, et al. Plasma surfactant protein-D as a diagnostic biomarker for acute respiratory distress syndrome: validation in US and Korean cohorts [J]. BMC Pulm Med, 2017, 17(1): 204.
66
Greene KE, Wright JR, Steinberg KP, et al. Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS [J]. Am J Respir Crit Care Med, 1999, 160(6): 1843-1850.
67
Jensen JS, Itenov TS, Thormar KM, et al. Prediction of non-recovery from ventilator-demanding acute respiratory failure, ARDS and death using lung damage biomarkers: data from a 1200-patient critical care randomized trial [J]. Ann Intensive Care, 2016, 6(1): 114.
68
Clark H, Reid K. The potential of recombinant surfactant protein D therapy to reduce inflammation in neonatal chronic lung disease, cystic fibrosis, and emphysema [J]. Arch Dis Child, 2003, 88(11): 981-984.
69
Todd DA, Marsh MJ, George A, et al. Surfactant phospholipids, surfactant proteins, and inflammatory markers during acute lung injury in children [J]. Pediatr Crit Care Med, 2010, 11(1): 82-91.
70
Du J, Abdel-Razek O, Shi Q, et al. Surfactant protein D attenuates acute lung and kidney injuries in pneumonia-induced sepsis through modulating apoptosis, inflammation and NF-kappaB signaling [J]. Sci Rep, 2018, 8(1): 15393.
71
支德源, 段美丽, 张淑文, 等. 脓毒症所致ARDS患者血浆肺表面活性蛋白D水平及其临床意义 [J]. 临床和实验医学杂志, 2013, 12(23): 1892-1895.
72
Sakamoto K, Hashimoto N, Kondoh Y, et al. Differential modulation of surfactant protein D under acute and persistent hypoxia in acute lung injury [J]. Am J Physiol Lung Cell Mol Physiol, 2012, 303(1): 43-53.
73
Schleich FN, Chevremont A, Paulus V, et al. Importance of concomitant local and systemic eosinophilia in uncontrolled asthma [J]. Eur Respir J, 2014, 44(1): 97-108.
74
Yousefi S, Sharma SK, Stojkov D, et al. Oxidative damage of SP-D abolishes control of eosinophil extracellular DNA trap formation [J]. J Leukoc Biol, 2018, 104(1): 205-214.
75
Brinker KG, Garner H, Wright JR. Surfactant protein A modulates the differentiation of murine bone marrow-derived dendritic cells [J]. Am J Physiol Lung Cell Mol Physiol, 2003, 284(1): 232-241.
76
Brandt EB, Mingler MK, Stevenson MD, et al. Surfactant protein D alters allergic lung responses in mice and human subjects [J]. J Allergy Clin Immunol, 2008, 121(5): 1140-1147.
77
Principe S, Benfante A, Battaglia S, et al. The potential role of SP-D as an early biomarker of severity of asthma [J]. J Breath Res, 2021, 15(4): 1001.
78
Valverde G, Zhou H, Lippold S, et al. A novel candidate region for genetic adaptation to high altitude in Andean populations [J]. PLoS One, 2015, 10(5): 125444.
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