Fibrosis in the central nervous system: from the meninges to the vasculature

被引:19
作者
Fehlberg, Corey R. [1 ]
Lee, Jae K. [1 ]
机构
[1] Univ Miami, Sch Med, Dept Neurol Surg, Miami Project Cure Paralysis, 1095 NW 14th Terrace,LPLC 4-19, Miami, FL 33136 USA
关键词
Fibrotic scar; Regeneration; Wound healing; Neuropathology; SPINAL-CORD-INJURY; EXTRACELLULAR-MATRIX; FIBROTIC SCAR; FUNCTIONAL RECOVERY; MOLECULAR-MECHANISMS; AXON REGENERATION; FIBROBLASTS FORM; GROWTH; TISSUE; LESIONS;
D O I
10.1007/s00441-021-03491-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Formation of a collagenous connective tissue scar after penetrating injuries to the brain or spinal cord has been described and investigated for well over 100 years. However, it was studied almost exclusively in the context of penetrating injuries that resulted in infiltration of meningeal fibroblasts, which raised doubts about translational applicability to most CNS injuries where the meninges remain intact. Recent studies demonstrating the perivascular niche as a source of fibroblasts have debunked the traditional view that a fibrotic scar only forms after penetrating lesions that tear the meninges. These studies have led to a renewed interest in CNS fibrosis not only in the context of axon regeneration after spinal cord injury, but also across a spectrum of CNS disorders. Arising with this renewed interest is some discrepancy about which perivascular cell gives rise to the fibrotic scar, but additional studies are beginning to provide some clarity. Although mechanistic studies on CNS fibrosis are still lacking, the similarities to fibrosis of other organs should provide important insight into how CNS fibrosis can be therapeutically targeted to promote functional recovery.
引用
收藏
页码:351 / 360
页数:10
相关论文
共 77 条
[2]  
Berry M, 1983, Acta Neurochir Suppl (Wien), V32, P31
[3]   Pharmacological modification of the extracellular matrix to promote regeneration of the injured brain and spinal cord [J].
Brazda, Nicole ;
Mueller, Hans Werner .
NEUROTHERAPY: PROGRESS IN RESTORATIVE NEUROSCIENCE AND NEUROLOGY, 2009, 175 :269-281
[4]   Untitled [J].
Brown, William R. ;
Thore, Clara R. .
BRAIN PATHOLOGY, 2011, 21 (03) :355-355
[5]   TGF-β1 and TGF-β2 expression after traumatic human spinal cord injury [J].
Buss, A. ;
Pech, K. ;
Kakulas, B. A. ;
Martin, D. ;
Schoenen, J. ;
Noth, J. ;
Brook, G. A. .
SPINAL CORD, 2008, 46 (05) :364-371
[6]   RELATION OF MILLIPORE TO HEALING AND REGENERATION IN TRANSECTED SPINAL CORDS OF MONKEYS [J].
CAMPBELL, JB ;
WINDLE, WF .
NEUROLOGY, 1960, 10 (03) :306-311
[7]   REGENERATION OF SEVERED NERVE FIBERS IN THE SPINAL CORD OF THE ADULT CAT [J].
CLEMENTE, CD ;
WINDLE, WF .
JOURNAL OF COMPARATIVE NEUROLOGY, 1954, 101 (03) :691-&
[8]   Fibronectin EDA forms the chronic fibrotic scar after contusive spinal cord injury [J].
Cooper, John G. ;
Jeong, Su Ji ;
McGuire, Tammy L. ;
Sharma, Sripadh ;
Wang, Wenxia ;
Bhattacharyya, Swati ;
Varga, John ;
Kessler, John A. .
NEUROBIOLOGY OF DISEASE, 2018, 116 :60-68
[9]   The Chemorepulsive Protein Semaphorin 3A and Perineuronal Net-Mediated Plasticity [J].
de Winter, F. ;
Kwok, J. C. F. ;
Fawcett, J. W. ;
Vo, T. T. ;
Carulli, D. ;
Verhaagen, J. .
NEURAL PLASTICITY, 2016, 2016
[10]   Reducing Pericyte-Derived Scarring Promotes Recovery after Spinal Cord Injury [J].
Dias, David Oliveira ;
Kim, Hoseok ;
Holl, Daniel ;
Solnestam, Beata Werne ;
Lundeberg, Joakim ;
Carlen, Marie ;
Goritz, Christian ;
Frisen, Jonas .
CELL, 2018, 173 (01) :153-+