What could be the function of the spinal muscular atrophy-causing protein SMN in macrophages?

被引:1
|
作者
Tapken, Ines [1 ,2 ]
Detering, Nora T. [1 ,2 ]
Claus, Peter [1 ,2 ]
机构
[1] SMATHERIA gGmbH, Nonprofit Biomed Res Inst, Hannover, Germany
[2] Ctr Syst Neurosci ZSN, Hannover, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
macrophage; monocyte; spinal muscular atrophy; SMA; SMN; SMN gene; neurodegeneration; DISEASE GENE-PRODUCT; MOTOR-NEURON PROTEIN; SINGLE NUCLEOTIDE; ARP2/3; COMPLEX; SURVIVAL; MOUSE; INTERACTS; ALTERS; MICE; DIFFERENTIATION;
D O I
10.3389/fimmu.2024.1375428
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Spinal Muscular Atrophy (SMA), a neurodegenerative disorder, extends its impact beyond the nervous system. The central protein implicated in SMA, Survival Motor Neuron (SMN) protein, is ubiquitously expressed and functions in fundamental processes such as alternative splicing, translation, cytoskeletal dynamics and signaling. These processes are relevant for all cellular systems, including cells of the immune system such as macrophages. Macrophages are capable of modulating their splicing, cytoskeleton and expression profile in order to fulfil their role in tissue homeostasis and defense. However, less is known about impairment or dysfunction of macrophages lacking SMN and the subsequent impact on the immune system of SMA patients. We aimed to review the potential overlaps between SMN functions and macrophage mechanisms highlighting the need for future research, as well as the current state of research addressing the role of macrophages in SMA.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] A Comparative Study of SMN Protein and mRNA in Blood and Fibroblasts in Patients with Spinal Muscular Atrophy and Healthy Controls
    Wadman, Renske I.
    Stam, Marloes
    Jansen, Marc D.
    van der Weegen, Yana
    Wijngaarde, Camiel A.
    Harschnitz, Oliver
    Sodaar, Peter
    Braun, Kees P. J.
    Dooijes, Dennis
    Lemmink, Henny H.
    van den Berg, Leonard H.
    van der Pol, W. Ludo
    PLOS ONE, 2016, 11 (11):
  • [42] Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy
    Sapaly, Delphine
    Dos Santos, Matthieu
    Delers, Perrine
    Biondi, Olivier
    Querol, Gwendoline
    Houdebine, Leo
    Khoobarry, Kevinee
    Girardet, Francois
    Burlet, Philippe
    Armand, Anne-Sophie
    Chanoine, Christophe
    Bureau, Jean-Francois
    Charbonnier, Frederic
    Lefebvre, Suzie
    SCIENTIFIC REPORTS, 2018, 8
  • [43] The Smn-Independent Beneficial Effects of Trichostatin A on an Intermediate Mouse Model of Spinal Muscular Atrophy
    Liu, Hong
    Yazdani, Armin
    Murray, Lyndsay M.
    Beauvais, Ariane
    Kothary, Rashmi
    PLOS ONE, 2014, 9 (07):
  • [44] Molecular analysis of SMN1 and NAIP genes in Egyptian patients with spinal muscular atrophy
    Essawi, M. L.
    Effat, L. K.
    Shanab, G. M. L.
    Al-Ettribi, G. M. M.
    El-Haronui, A. A.
    Karim, A. M.
    BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY, 2007, 108 (03): : 133 - 137
  • [45] Spinal muscular atrophy in Venezuela: quantitative analysis of SMN1 and SMN2 genes
    Yepez, Yuri
    Paradisi, Irene
    Arias, Sergio
    EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2020, 21 (01)
  • [46] Cerebellar structural, astrocytic, and neuronal abnormalities in the SMNΔ7 mouse model of spinal muscular atrophy
    Cottam, Nicholas C. C.
    Bamfo, Tiffany
    Harrington, Melissa A. A.
    Charvet, Christine J. J.
    Hekmatyar, Khan
    Tulin, Nikita
    Sun, Jianli
    BRAIN PATHOLOGY, 2023,
  • [47] Early heart failure in the SMNΔ7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery
    Bevan, Adam K.
    Hutchinson, Kirk R.
    Foust, Kevin D.
    Braun, Lyndsey
    McGovern, Vicki L.
    Schmelzer, Leah
    Ward, Jennifer G.
    Petruska, Jeffrey C.
    Lucchesi, Pamela A.
    Burghes, Arthur H. M.
    Kaspar, Brian K.
    HUMAN MOLECULAR GENETICS, 2010, 19 (20) : 3895 - 3905
  • [48] Liver SMN restoration rescues the Smn spinal muscular atrophy 2B/- mouse model of
    Sutton, Emma R.
    Beauvais, Ariane
    Yaworski, Rebecca
    De Repentigny, Yves
    Reilly, Aoife
    de Almeida, Alves
    Deguise, Marc-Olivier
    Poulin, Kathy L.
    Parks, Robin J.
    Schneider, Bernard L.
    Kothary, Rashmi
    EBIOMEDICINE, 2024, 110
  • [49] Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy
    Lutz, Cathleen M.
    Kariya, Shingo
    Patruni, Sunita
    Osborne, Melissa A.
    Liu, Don
    Henderson, Christopher E.
    Li, Darrick K.
    Pellizzoni, Livio
    Rojas, Jose
    Valenzuela, David M.
    Murphy, Andrew J.
    Winberg, Margaret L.
    Monani, Umrao R.
    JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (08) : 3029 - 3041
  • [50] Bone loss in survival motor neuron (Smn-/- SMN2) genetic mouse model of spinal muscular atrophy
    Shanmugarajan, Srinivasan
    Tsuruga, Eichi
    Swoboda, Kathryn J.
    Maria, Bernard L.
    Ries, William L.
    Reddy, Sakamuri V.
    JOURNAL OF PATHOLOGY, 2009, 219 (01) : 52 - 60