The Peripheral Lymphatic System Is Impaired by the Loss of Neuronal Control Associated with Chronic Spinal Cord Injury

被引:4
|
作者
Brunner, Georg [1 ]
Roux, Meike S. [2 ]
Falk, Thomas [3 ]
Bresch, Martina [3 ]
Boehm, Volker [1 ]
Bloedorn-Schlicht, Norbert [3 ]
Meiners, Thomas [1 ]
机构
[1] Werner Wicker Hosp, Ctr Spinal Cord Injuries, Bad Wildungen, Germany
[2] Fachklinik Hornheide, Dept Canc Res, Munster, France
[3] Dermatologikum Hamburg, Dept Dermatohistopathol, Hamburg, Germany
关键词
MOLECULAR CONTROL; PRESSURE ULCERS; LYMPHANGIOGENESIS; SKIN; VESSELS; ANGIOGENESIS; INFLAMMATION; VASCULATURE; DISRUPTION; TISSUES;
D O I
10.1016/j.ajpath.2022.06.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Spinal cord injury (SCI) is associated with venous vascular dysfunction below the level of injury, resulting in dysregulation of tissue fluid homeostasis in afflicted skin. The purpose of this study was to determine whether loss of neuronal control in chronic SCI also affects the skin lymphatic system. Morphology of lymphatics was characterized by immunohistochemistry and lymphatic gene expression profiles determined by DNA microarray analysis. In SCI, skin lymphatic function appeared to be impaired, because the ratio of functionally dilated versus collapsed lymphatic vessels was decreased 10 -fold compared with control. Consequently, the average lumen area of lymphatic vessels was almost halved, possibly due to the known impaired connective tissue integrity of SCI skin. In fact, collagenases were found to be overexpressed in SCI skin, and dermal collagen structure was impaired. Molecular profiling also suggested an SCI-specific phenotype of increased connective tissue turnover and decreased lymphatic contractility. The total number of lymphatic vessels in SCI skin, however, was doubled, pointing to enhanced lymphangiogenesis. In conclusion, these data show, for the first time, that lymphatic function and development in human skin are under neuronal control. Because peripheral venous and lymphatic vascular defects are associated with disturbed fluid homeostasis, inappropriate wound healing reactions, and impaired skin immunity, they might contribute to the predisposition of afflicted individuals to pressure ulcer formation and wound healing disorders. (Am J Pathol 2022, 192: 1448-1457; https://doi.org/10.1016/j.ajpath.2022.06.012)
引用
收藏
页码:1448 / 1457
页数:10
相关论文
共 50 条
  • [31] ROBUST AXONAL GROWTH AND A BLUNTED MACROPHAGE RESPONSE ARE ASSOCIATED WITH IMPAIRED FUNCTIONAL RECOVERY AFTER SPINAL CORD INJURY IN THE MRL/MpJ MOUSE
    Kostyk, S. K.
    Popovich, P. G.
    Stokes, B. T.
    Wei, P.
    Jakeman, L. B.
    NEUROSCIENCE, 2008, 156 (03) : 498 - 514
  • [32] Transcriptomic Analysis of Neuropathic Pain in the Mouse Spinal Cord Following Peripheral Nerve Injury
    Jiang, Lili
    Peng, Zhe
    Deng, Yuhui
    Chen, Peiyu
    Yu, Bingwei
    Guo, Miaosen
    Huang, Jinping
    JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS, 2022, 36 (05) : 1349 - 1358
  • [33] Hepatic dysfunction after spinal cord injury: A vicious cycle of central and peripheral pathology?
    Goodus, Matthew T.
    MeTigue, Dana M.
    EXPERIMENTAL NEUROLOGY, 2020, 325
  • [34] Greater daily leisure time physical activity is associated with lower chronic disease risk in adults with spinal cord injury
    Buchholz, Andrea C.
    Ginis, Kathleen A. Martin
    Bray, Steven R.
    Craven, B. Catharine
    Hicks, Audrey L.
    Hayes, Keith C.
    Latimer, Amy E.
    McColl, Mary Ann
    Potter, Patrick J.
    Wolfe, Dalton L.
    APPLIED PHYSIOLOGY NUTRITION AND METABOLISM, 2009, 34 (04) : 640 - 647
  • [35] Late blocking of peripheral TNF-α is ineffective after spinal cord injury in mice
    Vidal, Pia M.
    Lemmens, Evi
    Geboes, Lies
    Vangansewinkel, Tim
    Nelissen, Sofie
    Hendrix, Sven
    IMMUNOBIOLOGY, 2013, 218 (02) : 281 - 284
  • [36] Upregulation of Inflammatory Mediators in a Model of Chronic Pain after Spinal Cord Injury
    Rajat Sandhir
    Eugene Gregory
    Yong-Yue He
    Nancy E. J. Berman
    Neurochemical Research, 2011, 36 : 856 - 862
  • [37] Prognostic Value of Malondialdehyde (MDA) in the Temporal Progression of Chronic Spinal Cord Injury
    Haro Giron, Sergio
    Monserrat Sanz, Jorge
    Ortega, Miguel A.
    Garcia-Montero, Cielo
    Fraile-Martinez, Oscar
    Gomez-Lahoz, Ana M.
    Boaru, Diego Liviu
    de Leon-Oliva, Diego
    Guijarro, Luis G.
    Atienza-Perez, Mar
    Diaz, David
    Lopez-Dolado, Elisa
    Alvarez-Mon, Melchor
    JOURNAL OF PERSONALIZED MEDICINE, 2023, 13 (04):
  • [38] Dual neuronal response to tumor necrosis factor-alpha following spinal cord injury
    L.Creed Pettigrew
    David Grass
    James J.Hickman
    Mark S.Kindy
    Neural Regeneration Research, 2010, 5 (12) : 917 - 926
  • [39] Dual neuronal response to tumor necrosis factor-alpha following spinal cord injury
    Chi, Lingyi
    Yu, Jin
    Zhu, Hong
    Li, Xingang
    Zhu, Shugan
    Li, Zhenzhong
    Pettigrew, L. Creed
    Grass, David
    Hickman, James J.
    Kindy, Mark S.
    NEURAL REGENERATION RESEARCH, 2010, 5 (12) : 917 - 926
  • [40] Rapamycin increases neuronal survival, reduces inflammation and astrocyte proliferation after spinal cord injury
    Goldshmit, Yona
    Kanner, Sivan
    Zacs, Maria
    Frisca, Frisca
    Pinto, Alexander R.
    Currie, Peter D.
    Pinkas-Kramarski, Ronit
    MOLECULAR AND CELLULAR NEUROSCIENCE, 2015, 68 : 82 - 91