The cartilage matrisome in adolescent idiopathic scoliosis
Carol A. Wise , Diane Sepich , Aki Ushiki , Anas M. Khanshour , Yared H. Kidane , Nadja Makki , Christina A. Gurnett , Ryan S. Gray , Jonathan J. Rios , Nadav Ahituv , Lila Solnica-Krezel
Bone Research ›› 2020, Vol. 8 ›› Issue (1) : 13
The cartilage matrisome in adolescent idiopathic scoliosis
The human spinal column is a dynamic, segmented, bony, and cartilaginous structure that protects the neurologic system and simultaneously provides balance and flexibility. Children with developmental disorders that affect the patterning or shape of the spine can be at risk of neurologic and other physiologic dysfunctions. The most common developmental disorder of the spine is scoliosis, a lateral deformity in the shape of the spinal column. Scoliosis may be part of the clinical spectrum that is observed in many developmental disorders, but typically presents as an isolated symptom in otherwise healthy adolescent children. Adolescent idiopathic scoliosis (AIS) has defied understanding in part due to its genetic complexity. Breakthroughs have come from recent genome-wide association studies (GWAS) and next generation sequencing (NGS) of human AIS cohorts, as well as investigations of animal models. These studies have identified genetic associations with determinants of cartilage biogenesis and development of the intervertebral disc (IVD). Current evidence suggests that a fraction of AIS cases may arise from variation in factors involved in the structural integrity and homeostasis of the cartilaginous extracellular matrix (ECM). Here, we review the development of the spine and spinal cartilages, the composition of the cartilage ECM, the so-called “matrisome” and its functions, and the players involved in the genetic architecture of AIS. We also propose a molecular model by which the cartilage matrisome of the IVD contributes to AIS susceptibility.
| [1] |
Herring J. (ed.) Tachdjian’s Pediatric Orthopaedics. 5th edn. (WB Saunders, Philadelphia, 2013). |
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
Weinstein, S. L., Dolan, L. A., Wright, J. G. & Dobbs, M. B. Effects of bracing in adolescents with idiopathic scoliosis. N . Engl. J. Med. 369, 1515–1521 (2013). |
| [9] |
|
| [10] |
Wise, C. A. The genetic architecture of idiopathic scoliosis. in Molecular Genetics of Pediatric Orthopaedic Disorders. (eds Carol, A. & Wise, J. J. R.) 71–90 (Springer, New York, 2014). |
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
Dunwoodie SaSD. Genetic and environmental interaction in malformation of the vertebral column. in Molecular genetics of pediatric orthopaedic disorders. (eds Carol, A. & Wise, J. J. R.) 131–151 (Springer, New York, 2015). |
| [20] |
Turnpenny, P. D. Classification and etiologic dissection of vertebral segmentation anomalies. in Molecular genetics of pediatric orthopaedic disorders. (eds Carol, A. & Wise, J. J. R.) 105–130 (Springer, New York, 2015). |
| [21] |
|
| [22] |
|
| [23] |
|
| [24] |
|
| [25] |
|
| [26] |
|
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
|
| [41] |
|
| [42] |
|
| [43] |
|
| [44] |
|
| [45] |
|
| [46] |
|
| [47] |
|
| [48] |
|
| [49] |
|
| [50] |
|
| [51] |
|
| [52] |
|
| [53] |
|
| [54] |
|
| [55] |
|
| [56] |
|
| [57] |
|
| [58] |
|
| [59] |
|
| [60] |
|
| [61] |
|
| [62] |
|
| [63] |
|
| [64] |
|
| [65] |
|
| [66] |
|
| [67] |
|
| [68] |
|
| [69] |
|
| [70] |
|
| [71] |
|
| [72] |
|
| [73] |
|
| [74] |
|
| [75] |
|
| [76] |
|
| [77] |
|
| [78] |
|
| [79] |
|
| [80] |
|
| [81] |
|
| [82] |
|
| [83] |
|
| [84] |
|
| [85] |
|
| [86] |
|
| [87] |
|
| [88] |
|
| [89] |
|
| [90] |
|
| [91] |
Nebert, D. W. Z. L. SLC39A8 gene encoding a metal ion transporter: discovery and bench to bedside. Hum. Genet. 13, 51 (2019). |
| [92] |
|
| [93] |
|
| [94] |
|
| [95] |
|
| [96] |
|
| [97] |
Long, F., Zhang, X. M., Karp, S., Yang, Y. & McMahon, A. P. Genetic manipulation of hedgehog signaling in the endochondral skeleton reveals a direct role in the regulation of chondrocyte proliferation. Development. 128, 5099–5108 (2001). |
| [98] |
|
| [99] |
|
| [100] |
|
| [101] |
|
| [102] |
|
| [103] |
|
| [104] |
|
| [105] |
|
| [106] |
|
| [107] |
|
| [108] |
|
| [109] |
|
| [110] |
|
| [111] |
|
U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)(P01HD084387)
Texas Scottish Rite Hospital Research Fund
U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)(R01AR067715)
U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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