Brain samples from the Central South University Xiangya Human Brain Bank

ZHANG Qi-lei WANG Jian ZHANG Xiao-jie ZHANG Yan WANG Xiao-ping PAN Ai-hua YAN Xiao-xin

Acta Anatomica Sinica ›› 2026, Vol. 57 ›› Issue (3) : 280-289.

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Acta Anatomica Sinica ›› 2026, Vol. 57 ›› Issue (3) : 280-289. DOI: 10.16098/j.issn.0529-1356.2026.03.002
Neurbiology

Brain samples from the Central South University Xiangya Human Brain Bank

  • ZHANG  Qi-lei1  WANG  Jian2,3 ZHANG  Xiao-jie4  ZHANG  Yan4 WANG  Xiao-ping4  PAN  Ai-hua1*  YAN  Xiao-xin1*
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Abstract

 Objective  To analyze the donated brain samples received by the Xiangya Brain Bank of Central South University, and further establish a systematic mechanism for tissue acquisition, sample preservation, pathological diagnosis, and global sharing, in order to promote the construction of the Chinese brain bank, and provide key support for neuroscience and neurological disease research.  Methods  Based on the body donation program in Xiangya School of Medicine of Central South University, we collected and analyzed 373 postmortem human brains from 2016 to 2025, with neuropathological assessments performed according to international and domestic diagnostic protocols.  Results  Donors spanned a broad age range, from infancy to advanced old age. The annual number of brain donations exhibited an overall upward trend, accompanied by a progressive reduction in postmortem delay and generally well-preserved RNA quality. Systematic neuropathological evaluation revealed that the cohort was predominantly composed of cases with Alzheimer’s disease neuropathological change (ADNC) and primary age-related tauopathy (PART), characterized by typical intermediate-stage pathological features and a distinct age-dependent distribution, respectively.   Conclusion  Xiangya Brain Bank is a key part of China’s human brain resource network and has supported neuroanatomical, neuropathological and translational research across the nation. With continuous efforts in standardized histological processing, resource sharing, and international collaboration, human brain banking will become a firmer cornerstone for basic, translational and clinical neuroscience in China.

Key words

/ "> Human Brain Bank│ Donor demographic characteristics│Quality control information│Neurological disease│ Neuropathological diagnosis│ Human

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ZHANG Qi-lei WANG Jian ZHANG Xiao-jie ZHANG Yan WANG Xiao-ping PAN Ai-hua YAN Xiao-xin. Brain samples from the Central South University Xiangya Human Brain Bank[J]. Acta Anatomica Sinica. 2026, 57(3): 280-289 https://doi.org/10.16098/j.issn.0529-1356.2026.03.002

References

[1] Chung K, Deisseroth K. CLARITY for mapping the nervous system [J]. Nat Methods, 2013, 10(6): 508-513.
[2] Kang HJ, Kawasawa YI, Cheng F, et al. Spatio-temporal transcriptome of the human brain [J]. Nature, 2011, 478(7370): 483-489.
[3] Samarasekera N, Salman RA, Huitinga I, et al. Brain banking for neurological disorders [J]. Lancet Neurol, 2013, 12(11): 1096-1105.
[4] Zeng H, Shen EH, Hohmann JG, et al. Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures [J]. Cell, 2012, 149(2): 483-496.
[5] Ravid R, Park YM. Brain banking in the twenty-first century: creative solutions and ongoing challenges [J]. J Biorepos Sci Appl Med, 2014, 2: 17-27.
[6] Ma  C, Bao AM, Yan XX, et al. Progress in Human Brain Banking in China[J]. Neurosci Bull, 2019, 35(2): 179-182.
[7] Qiu WY, Ma Ch,  Bao AM, et al. Standardized operation protocol for the Chinese Human Brain Bank [J]. Acta Anatomica Sinica, 2017, 48(3): 334-341.(in Chinese)
仇文颖,马超,包爱民等. 中国人脑组织库标准化操作方案 [J]. 解剖学报, 2017, 48(3): 334-341.
[8] Qiu W, Zhang H, Bao A, et al. Standardized Operational Protocol for Human Brain Banking in China [J]. Neurosci Bull, 2019, 35(2): 270-276.
[9] Wang X, Chen Zh, Wu JL, et al. Standardized operation protocol for the Chinese Human Brain Bank Collaborative Alliance, 2nd Edition [J]. Acta Anatomica Sinica, 2024, 55(6): 734-745.(in Chinese)
王雪, 陈震, 吴娟利, 等. 中国人脑组织库协作联盟标准化操作方案第2版 [J]. 解剖学报, 2024, 55(6): 734-745.
[10] Zhou D, Zhou Y, Sun Z, et al. The China brain multi-omics atlas project (CBMAP) [J]. Mol Psychiatry, 2026, 31(1): 591-598.
[11] Hu X, Hu Z L, Li Z, et al. Sortilin fragments deposit at senile plaques in human cerebrum [J]. Front Neuroanat, 2017, 11: 45.
[12] Tu T, Cai XL, Sun ZP, et al. Mossy fiber expression of αSMA in human hippocampus and its relevance to brain evolution and neuronal development [J]. Sci Rep, 2025, 15(1): 15834.
[13] Jiang J, Yang C, Ai JQ, et al. Intraneuronal sortilin aggregation relative to granulovacuolar degeneration, tau pathogenesis and sorfra plaque formation in human hippocampal formation [J]. Front Aging Neurosci, 2022, 14: 926904.
[14] Doher N, Davoudi V, Magaki S, et al. Illustrated neuropathologic diagnosis of Alzheimer’s disease [J]. Neurol Int, 2023,15(3):857-867.
[15] Klioueva NM, Rademaker MC, Dexter DT, et al. BrainNet Europe’s Code of Conduct for brain banking [J]. J Neural Transm (Vienna), 2015, 122(7): 937-940.
[16] Li Z, Bian Y, Zeng L, et al. Life expectancy, causes of death, risk factors in China and the U.S [J]. Ann Glob Health, 2017, 83(3-4): 407-414.
[17] Zou H, Li Z, Tian X, et al. The top 5 causes of death in China from 2000 to 2017 [J]. Sci Rep, 2022, 12(1): 8119.
[18] Miyahara K, Hino M, Yu Z, et al. The influence of tissue pH and RNA integrity number on gene expression of human postmortem brain [J]. Front Psychiatry, 2023, 14: 1156524.
[19] Monoranu CM, Apfelbacher M, Grünblatt E, et al. pH measurement as quality control on human post mortem brain tissue: a study of the BrainNet Europe consortium [J]. Neuropathol Appl Neurobiol, 2009, 35(3): 329-337.
[20] Zheng L, Duan J, Duan X, et al. Association of apolipoprotein E (ApoE) polymorphism with Alzheimer’s disease in Chinese population [J]. Curr Alzheimer Res, 2016, 13(8): 912-917.
[21] Li Z, Shue F, Zhao N, et al. APOE2: protective mechanism and therapeutic implications for Alzheimer’s disease [J]. Mol Neurodegener, 2020, 15(1): 63.
[22] Zhang QL, Liu Y, Tu T, et al. The comorbidity of AD and PD: exploring clinical, pathological, and biomarker interactions [J]. Aging Dis, 2025. doi: 10.14336/AD.2025.0301. Epub ahead of print. PMID: 40540716.
[23] Rademaker MC, de Lange GM, Palmen SJMC. The Netherlands Brain Bank for psychiatry[J]. Handb Clin Neurol, 2018, 150:3-16.
[24] Mekkes NJ, Groot M, Hoekstra E, et.al. Identification of clinical disease trajectories in neurodegenerative disorders with natural language processing [J]. Nat Med, 2024, 30(4):1143-1153.
[25] Leonenko G, Bauermeister S, Ghanti D, et al. Dementias platform UK: Bringing genetics into life [J]. Alzheimers Dement, 2024, 20(5): 3281-3289.
[26] Tendler BC, Hanayik T, Ansorge O, et al. The Digital Brain Bank, an open access platform for post-mortem imaging datasets [J]. ELife, 2022, 11: e73153.
[27] Harrison PJ. The neuropathology of primary mood disorder [J]. Brain, 2002, 125(Pt 7): 1428-1449.
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