[1] |
Singer SJ. Preparation of an electron-dense antibody conjugate [J]. Nature, 1959, 183(4674): 1523-1524.
|
[2] |
Roth J, Bendayan M, Orci L. Ultrastructural localization of intracellular antigens by the use of protein A-gold complex [J]. J Histochem Cytochem, 1978, 26(12): 1074-1081.
|
[3] |
Kim HL, Riew TR, Park J, et al. Correlative light and electron microscopy using frozen section obtained using cryo-ultramicrotomy [J]. Int J Mol Sci, 2021, 22(8): 4273.
|
[4] |
Najafian B, Lusco MA, Alpers CE, et al. Approach to kidney biopsy: core curriculum 2022 [J]. Am J Kidney Dis, 2022, 80(1): 119-131.
|
[5] |
Gertz MA. Immunoglobulin light chain amyloidosis: 2022 update on diagnosis, prognosis, and treatment [J]. Am J Hematol, 2022, 97(6): 818-829.
|
[6] |
Sethi S, Rajkumar SV, D′agati VD. The complexity and heterogeneity of monoclonal immunoglobulin-associated renal diseases [J]. J Am Soc Nephrol, 2018, 29(7): 1810-1823.
|
[7] |
Said SM, Best Rocha A, Valeri AM, et al. The characteristics of patients with kidney light chain deposition disease concurrent with light chain amyloidosis [J]. Kidney Int, 2022, 101(1): 152-163.
|
[8] |
Kanzaki G, Okabayashi Y, Nagahama K, et al. Monoclonal immunoglobulin deposition disease and related diseases [J]. J Nippon Med Sch, 2019, 86(1): 2-9.
|
[9] |
Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee [J]. Amyloid, 2018, 25(4): 215-219.
|
[10] |
陈思羽,韩伟霞,王晨. 肾淀粉样变性病的病理诊断与分型、分级的研究进展[J/CD]. 中华肾病研究电子杂志,2020, 9 (2): 86-89.
|
[11] |
Satoskar AA, Burdge K, Cowden DJ, et al. Typing of amyloidosis in renal biopsies: diagnostic pitfalls [J]. Arch Pathol Lab Med, 2007, 131(6): 917-922.
|
[12] |
Lachmann HJ, Booth DR, Booth SE, et al. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis [J]. N Engl J Med, 2002, 346(23): 1786-1791.
|
[13] |
Abildgaard N, Rojek AM, Moller HE, et al. Immunoelectron microscopy and mass spectrometry for classification of amyloid deposits [J]. Amyloid, 2020, 27(1): 59-66.
|
[14] |
Heilman RL, Velosa JA, Holley KE, et al. Long-term follow-up and response to chemotherapy in patients with light-chain deposition disease [J]. Am J Kidney Dis, 1992, 20(1): 34-41.
|
[15] |
Wang Q, Jiang F, Xu G. The pathogenesis of renal injury and treatment in light chain deposition disease [J]. J Transl Med, 2019, 17(1): 387.
|
[16] |
王梅,王英,王素霞,等. 早期轻链沉积病的诊断 [J]. 中华肾脏病杂志,2004, 20(2): 87-89.
|
[17] |
王素霞,邹万忠,王梅,等. 肾轻链沉积病和轻链型淀粉样变的电镜及免疫电镜研究 [J]. 北京大学学报(医学版), 2003, 35(6): 576-580.
|
[18] |
Fogo AB, Lusco MA, Najafian B, et al. AJKD atlas of renal pathology: light chain proximal tubulopathy [J]. Am J Kidney Dis, 2016, 67(2): e9-e10.
|
[19] |
Büttner-Herold M, Krieglstein N, Chuva T, et al. Light chain restriction in proximal tubules-implications for light chain proximal tubulopathy [J]. Front Med (Lausanne), 2022, 9: 723758.
|
[20] |
Li XM, Xu F, Liang DD, et al. Clinicopathologic characteristics of light chain proximal tubulopathy with light chain inclusions involving multiple renal cell types [J]. Clin Nephrol, 2018, 89(2): 83-92.
|
[21] |
Kapur U, Barton K, Fresco R, et al. Expanding the pathologic spectrum of immunoglobulin light chain proximal tubulopathy [J]. Arch Pathol Lab Med, 2007, 131(9): 1368-1372.
|
[22] |
Gu X, Barrios R, Cartwright J, et al. Light chain crystal deposition as a manifestation of plasma cell dyscrasias: the role of immunoelectron microscopy [J]. Hum Pathol, 2003, 34(3): 270-277.
|
[23] |
Hoxha E, Reinhard L, Stahl RAK. Membranous nephropathy: new pathogenic mechanisms and their clinical implications [J]. Nat Rev Nephrol, 2022, 18(7): 466-478.
|
[24] |
Prunotto M, Carnevali ML, Candiano G, et al. Autoimmunity in membranous nephropathy targets aldose reductase and SOD2 [J]. J Am Soc Nephrol, 2010, 21(3): 507-519.
|
[25] |
Gödel M, Grahammer F, Huber TB. Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy [J]. N Engl J Med, 2015, 372(11): 1073-10755.
|
[26] |
Herwig J, Skuza S, Sachs W, et al. Thrombospondin type 1 domain-containing 7A localizes to the slit diaphragm and stabilizes membrane dynamics of fully differentiated podocytes [J]. J Am Soc Nephrol, 2019, 30(5): 824-839.
|
[27] |
Rodrigues JC, Haas M, Reich HN. IgA nephropathy [J]. Clin J Am Soc Nephrol, 2017, 12(4): 677-686.
|
[28] |
Lai KN, Tang SC, Schena FP, et al. IgA nephropathy [J]. Nat Rev Dis Primers, 2016, 2: 16001.
|
[29] |
Nishioka R, Hara S, Kawahara H, et al. Glomerulonephritis with severe nephrotic syndrome induced by immune complexes composed of galactose-deficient IgA1 in primary Sjogren′s syndrome: a case report [J]. BMC Nephrol, 2021, 22(1): 108.
|
[30] |
Dysart NK Jr, Sisson S, Vernier RL. Immunoelectron microscopy of IgA nephropathy [J]. Clin Immunol Immunopathol, 1983, 29(2): 254-270.
|
[31] |
王素霞,邹万忠,杨莉,等. 膜性肾病合并IgA肾病的临床病理特点[J]. 中华病理学杂志,2007, 36(3): 171-174.
|
[32] |
Sjowall C, Olin AI, Skogh T, et al. C-reactive protein, immunoglobulin G and complement co-localize in renal immune deposits of proliferative lupus nephritis [J]. Autoimmunity, 2013, 46(3): 205-214.
|
[33] |
Horvei KD, Pedersen HL, Fismen S, et al. Lupus nephritis progression in FcγRIIB-/-yaa mice is associated with early development of glomerular electron dense deposits and loss of renal DNase I in severe disease [J]. PLoS One, 2017, 12(11): e0188863.
|
[34] |
Grahammer F, Wigge C, Schell C, et al. A flexible, multilayered protein scaffold maintains the slit in between glomerular podocytes [J]. JCI Insight, 2016, 1(9): e86177.
|
[35] |
Yuan HP, Takeuchi E, Taylor GA, et al. Nephrin dissociates from actin, and its expression is reduced in early experimental membranous nephropathy [J]. J Am Soc Nephrol, 2002, 13(4): 946-956.
|
[36] |
Roselli S, Gribouval O, Boute N, et al. Podocin localizes in the kidney to the slit diaphragm area [J]. Am J Pathol, 2002, 160(1): 131-139.
|
[37] |
La TM, Tachibana H, Li SA, et al. Dynamin 1 is important for microtubule organization and stabilization in glomerular podocytes [J]. FASEB J, 2020, 34(12): 16449-16463.
|
[38] |
Sachs M, Wetzel S, Reichel TJ, et al. ADAM10-mediated ectodomain shedding is an essential driver of podocyte damage [J]. J Am Soc Nephrol, 2021, 32(6): 1389-1408.
|
[39] |
Nielsen R, Christensen EI, Birn H. Megalin and cubilin in proximal tubule protein reabsorption: from experimental models to human disease [J]. Kidney Int, 2016, 89(1): 58-67.
|
[40] |
Sun J, Hultenby K, Axelsson J, et al. Proximal tubular expression patterns of megalin and cubilin in proteinuric nephropathies [J]. Kidney Int Rep, 2017, 2(4): 721-732.
|
[41] |
胡小影. MC1R在肾脏中表达定位及AKI模型肾组织中的表达变化研究 [D]. 郑州:郑州大学,2021.
|
[42] |
Cao Y, Zhang Y, Wang S, et al. Detection of the hepatitis C virus antigen in kidney tissue from infected patients with various glomerulonephritis [J]. Nephrol Dial Transplant, 2009, 24(9): 2745-2751.
|
[43] |
Stamatiades EG, Tremblay ME, Bohm M, et al. Immune monitoring of trans-endothelial transport by kidney-resident macrophages [J]. Cell, 2016, 166(4): 991-1003.
|
[44] |
李红梅,张勤奋,李茵茵,等. 透射电镜和光镜联合应用于细胞观察[J]. 实验室研究与探索,2019, 38(11): 18-20, 65.
|
[45] |
Nasr SH, Fogo AB. New developments in the diagnosis of fibrillary glomerulonephritis [J]. Kidney Int, 2019, 96(3): 581-592.
|