Periostin-like-factor and Periostin in an animal model of work-related musculoskeletal disorder

Bone

Volumn 44, Issue 3, 2009, Pages 502-512

  Rani, Shobha ^a   Barbe, Mary F ^a,c   Barr, Ann E ^b   Litvin, Judith ^a  

^a TEMPLE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b THOMAS JEFFERSON UNIVERSITY   (United States)

^c TEMPLE UNIVERSITY   (United States)

Author keywords

Bone; Epiphyseal plate; Periosteum; Periostin; Periostin like factor; Work related musculoskeletal disorder

Indexed keywords

OSTEOCALCIN; TRANSCRIPTION FACTOR RUNX2;

ANIMAL EXPERIMENT; ARTICLE; BONE REMODELING; CONTROLLED STUDY; FEMALE; IMMUNOHISTOCHEMISTRY; MUSCULOSKELETAL DISEASE; NONHUMAN; OSSIFICATION; OSTEOBLAST; PERIOSTEUM; PROTEIN LOCALIZATION; RAT;

ANIMALS; BEHAVIOR, ANIMAL; BIOLOGICAL MARKERS; CELL ADHESION MOLECULES; CUMULATIVE TRAUMA DISORDERS; DISEASE MODELS, ANIMAL; FEMALE; HUMANS; MUSCLE PROTEINS; MUSCULOSKELETAL DISEASES; PERIOSTEUM; PHYSICAL EXERTION; RADIUS; RANDOM ALLOCATION; RATS; RATS, SPRAGUE-DAWLEY; STRESS, MECHANICAL; ULNA;

EID: 59649103810     PISSN: 87563282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bone.2008.11.012     Document Type: Article

References (68)

1. Zinn K., McAllister L., and Goodman C.S. Sequence analysis and neuronal expression of fasciclin I in grasshopper and Drosophila. Cell 53 4 (1988) 577-587
2. Litvin J., Zhu S., Norris R., and Markwald R. The periostin family of proteins: therapeutic targets for heart disease. Anat. Rec. 287 2 (2005) 1205-1212
3. Coutu D.L., Wu J.H., Monette A., Rivard G.E., Blostein M.D., and Galipeau J. Periostin, a member of a novel family of vitamin K-dependent proteins, is expressed by mesenchymal stromal cells. J. Biol. Chem. 283 26 (2008) 17991-18001 Epub 2008 Apr 30
4. Huber O., and Sumper M. Algal-CAMs: isoforms of a cell adhesion molecule in embryos of the alga Volvox with homology to Drosophila fasciclin I. EMBO. J. 13 18 (1994) 4212-4222
5. Terasaka K., Yamaguchi R., Matsuo K., Yamazaki A., Nagai S., and Yamada T. Complete nucleotide sequence of immunogenic protein MPB70 from Mycobacterium bovis BCG. FEMS. Microbiol. Lett. 49 2-3 (1989) 273-276
6. Politz O., Gratchev A., McCourt P.A., Schledzewski K., Guillot P., Johansson S., et al. Stabilin-1 and -2 constitute a novel family of fasciclin-like hyaluronan receptor homologues. Biochem. J. 362 1 (2002) 155-164
7. Skonier J., Neubauer M., Madisen L., Bennett K., Plowman G.D., and Purchio A.F. CDNA cloning and sequence analysis of ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta. DNA. Cell Biol. 11 (1992) 511-522
8. Horiuchi K., Amizuka N., Takeshita S., Takamatsu H., Katsuura M., Ozawa H., et al. Identification and characterization of a novel protein, Periostin, with restricted expression to periosteum and periodontal ligament and increased expression by transforming growth factor beta. J. Bone. Miner. Res. 14 (1999) 1239-1249
9. Litvin J., Selim A., Montgomery M., Lehmann K., Devlin H., Bednarik D., et al. Expression and function of periostin-isoforms in bone. J. Biol. Chem. 92 (2004) 1044-1061
10. Katsuragi N., Morishita R., Nakamura N., Ochiai T., Taniyama Y., Hasegawa Y., et al. Periostin as a novel factor responsible for ventricular dilation. Circulation 110 (2004) 1806-1813
11. Kii I., Amizuka N., Minqi L., Kitajima S., Saga Y., and Kudo A. Periostin is an extracellular matrix protein required for eruption of incisors in mice. Biochem. Biophys. Res. Commun. 342 (2006) 766-772
12. Kruzynska-Frejtag A., Wang J., Maeda M., Rogers R., Krug E., Hoffman S., et al. Periostin is expressed within the developing teeth at the sites of epithelial-mesenchymal interaction. Dev. Dyn. 229 (2004) 857-868
13. Lallier T.E., and Spencer A. Use of microarrays to find novel regulators of periodontal ligament fibroblast differentiation. Cell Tissue Res. 327 (2007) 93-109
14. Suzuki H., Amizuka N., Kii I., Kawano Y., Nozawa-Inoue K., Suzuki A., et al. Immunohistochemical localization of periostin in tooth and its surrounding tissues in mouse mandibles during development. Anat. Rec. A. Discov. Mol. Cell. Evol. Biol. 281 (2004) 1264-1275
15. Kruzynska-Frejtag A., Machnicki M., Rogers R., Markwald R.R., and Conway S.J. Periostin (an osteoblast specific factor) is expressed within the embryonic mouse heart during valve formation. Mech. Dev. 103 (2001) 183-188
16. Norris R.A., Kern C.B., Wessels A., Moralez E.I., Markwald R.R., and Mjaatvedt C.H. Identification and detection of the periostin gene in cardiac development. Anat. Rec. A. Discov. Mol. Cell. Evol. Biol. 281 2 (2004) 1227-1233
17. Norris R.A., Kern C.B., Wessels A., Wirrig E.E., Markwald R.R., and Mjaatvedt C.H. Detection of betaig-H3, a TGFbeta induced gene, during cardiac development and its complementary pattern with periostin. Anat. Embryol. (Berl) 210 1 (2005) 13-23
18. Kern C.B., Hoffman S., Moreno R., Damon B.J., Norris R.A., Krug E.L., et al. Immunolocalization of chick periostin protein in the developing heart. Anat. Rec. A. Discov. Mol. Cell. Evol. Biol. 284 (2005) 415-423
19. Lindsley A., Li W., Wang J., Maeda N., Rogers R., and Conway S.J. Comparison of the four mouse fasciclin-containing genes expression patterns during valvuloseptal morphogenesis. Gene. Expr. Patterns. 5 (2005) 593-600
20. Litvin J., Blagg A., Mu A., Matiwala S., Montgomery M., Berretta R., et al. Periostin and Periostin-like factor in the human heart: possible therapeutic targets. Cardiovasc. Pathol. 15 1 (2006) 24-32
21. Litvin J., Chen X., Keleman S., Zhu S., and Autieri M. Expression and function of periostin-like factor in vascular smooth muscle cells. Am. J. Physiol. Cell. Physiol. 292 5 (2007) C1672-C1680 Epub 2006 Nov 8
22. Lindner V., Wang Q., Conley B.A., Friesel R.E., and Vary C.P. Vascular injury induces expression of periostin: implications for vascular cell differentiation and migration. Arterioscler. Thromb. Vasc. Biol. 25 (2005) 77-83
23. Stanton L.W., Garrard L.J., Damm D., Garrick B.L., Lam A., Kapoun A.M., et al. Altered patterns of gene expression in response to myocardial infarction. Circ. Res. 86 (2000) 934-939
24. Wang D., Oparil S., Feng J.A., Li P., Perry G., Chen L.B., et al. Effects of pressure overload on extracellular matrix expression in the heart of the atrial natriuretic peptide-null mouse. Hypertension 42 (2003) 88-95
25. Choi P., Jordan C.D., Mendez E., Houck J., Yueh B., Farwell D.G., et al. Examination of oral cancer biomarkers by tissue microarray analysis. Arch. Otolaryngol. Head Neck Surg. 34 5 (2008) 539-546
26. Fukushima N., Kikuchi Y., Nishiyama T., Kudo A., and Fukayama M. Periostin deposition in the stroma of invasive and intraductal neoplasms of the pancreas. Mod. Pathol. 21 8 (2008) 1044-1053
27. Kudo Y., Ogawa I., Kitajima S., Kitagawa M., Kawai H., Gaffney P.M., et al. Periostin promotes invasion and anchorage-independent growth in the metastatic process of head and neck cancer. Cancer Res. 66 14 (2006) 6928-6935
28. Sasaki H., Auclair D., Kaji M., Fukai I., Kiriyama M., Yamakawa Y., et al. Serum level of the periostin, a homologue of an insect cell adhesion molecule, in thymoma patients. Cancer Lett. 172 (2001) 34-37
29. Crnogorac-Jurcevic T., Missiaglia E., Blaveri E., Gangeswaran R., Jones M., Terris B., et al. Molecular alterations in pancreatic carcinoma: expression profiling shows that dysregulated expression of S100 genes is highly prevalent. J. Pathol. 201 1 (2003) 63-74
30. Tilman G., Mattiussi M., Brasseur F., van Baren N., and Decottignies A. Human periostin gene expression in normal tissues, tumors and melanoma: evidences for Periostin production by both stromal and melanoma cells. Mol. Cancer 17 6 (2007) 80
31. Lal A., Lash A.E., Altschul S.F., Velculescu V., Zhang L., McLendon R.E., et al. A public database for gene expression in human cancers. Cancer Res. 59 21 (1999) 5403-5407
32. Sasaki H., Yu C.Y., Dai M., Tam C., Loda M., Auclair D., et al. Elevated serum periostin levels in patients with bone metastases from breast but not lung cancer. Breast Cancer Res. Treat. 77 3 (2003) 245-252
33. Shao R., Bao S., Bai X., Blanchette C., Anderson R.M., Dang T., et al. Acquired expression of periostin by human breast cancers promotes tumor angiogenesis through up-regulation of vascular endothelial growth factor receptor 2 expression. Mol. Cell Biol. 24 9 (2004) 3992-4003
34. Puglisi F., Puppin C., Pegolo E., Andreetta C., Pascoletti G., D'Aurizio F., et al. Expression of periostin in human breast cancer. J. Clin. Pathol. 61 4 (2008) 494-498
35. Sasaki H., Auclair D., Fukai I., Kiriyama M., Yamakawa Y., Fujii Y., et al. Serum level of the periostin, a homologue of an insect cell adhesion molecule, as a prognostic marker in non-small cell lung carcinomas. Cancer 92 4 (2001) 843-848
36. Matei D., Graeber T.G., Baldwin R.L., Karlan B.Y., Rao J., and Chang D.D. Gene expression in epithelial ovarian carcinoma. Oncogene 21 41 (2002) 6289-6298
37. Bao S., Ouyang G., Bai X., Huang Z., Ma C., Liu M., et al. Periostin potently promotes metastatic growth of colon cancer by augmenting cell survival via the Akt/PKB pathway. Cancer Cell 5 4 (2004) 329-339
38. Kikuchi Y., Kashima T.G., Nishiyama T., Shimazu K., Morishita Y., Shimazaki M., et al. Periostin is expressed in pericryptal fibroblasts and cancer-associated fibroblasts in the colon. J. Histochem. Cytochem. 56 8 (2008) 753-764
39. Yoshioka N., Fuji S., Shimakage M., Kodama K., Hakura A., Yutsudo M., et al. Suppression of anchorage-independent growth of human cancer cell lines by the TRIF52/periostin/OSF-2 gene. Exp. Cell Res. 279 1 (2002) 91-99
40. Erkan M., Kleeff J., Gorbachevski A., Reiser C., Mitkus T., Esposito I., et al. Periostin creates a tumor-supportive microenvironment in the pancreas by sustaining fibrogenic stellate cell activity. Gastroenterology 132 4 (2007) 1447-1464
41. Oku E., Kanaji T., Takata Y., Oshima K., Seki R., Morishige S., et al. Periostin and bone marrow fibrosis. Int. J. Hematol. 88 1 (2008) 57-63
42. Takayama G., Arima K., Kanaji T., Toda S., Tanaka H., Shoji S., et al. Periostin: a novel component of subepithelial fibrosis of bronchial asthma downstream of IL-4 and IL-13 signals. J. Allergy Clin. Immunol. 118 1 (2006) 98-104
43. Norris R.A., Damon B., Mironov V., Kasyanov V., Ramamurthi A., Moreno-Rodriguez R., et al. Periostin regulates collagen fibrillogenesis and the biomechanical properties of connective tissues. J. Cell. Biochem. 101 3 (2007) 695-711
44. Zhu S, Barbe MF, Liu C, Hadjiargyrou M, Popoff SN, Rani S, Safadi FF, Litivn J. Periostin-like-factor in Osteogenesis. Journal of Cellular Physiology. 2008. In Press. J Cell Physiol.
45. Bureau of Labor Statistics. Lost-work time injuries and illnesses: characteristics and resulting, days away from work. United States Department of Labor News USDL (2005) 05-521
46. Bernard. In: Bernard B.P. (Ed). Musculoskeletal Disorders (MSDs) and Workplace factors: A Critical Review of Epidemiological Evidence for Work-related Musculoskeletal Disorders of the Neck, Upper Extremity, and Low Back (1997), U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control. National Institute for Occupational Safety and Health, Cincinnati, OH (1997) Publication no. 97-141
47. National Research Council and Institute of Medicine. Musculoskeletal Disorders and the Workplace (2001), National Academy Press, Washington, DC 57-59
48. Barbe M.F., Barr A.E., Gorzelany I., Amin M., Gaughan J.P., and Safadi F.F. Chronic repetitive reaching and grasping results in decreased motor performance and widespread tissue responses in a rat model of MSD. J. Orthop. Res. 21 (2003) 167-176
49. Clark B.D., Al-Shatti T., Barr A.E., Amin M., and Barbe M.F. Performance of a high-repetition, high-force task induces carpel tunnel syndrome in rats. J. Orthop. Sports. Phys. Ther. 34 (2004) 244-253
50. Clark B.D., Barr A.E., Safadi F.F., Beitman L., Al-Shatti T., Amin M., et al. Median nerve trauma in a rat model of work-related musculoskeletal disorder. J. Neurotrauma. 20 (2003) 681-695
51. Barr A.E., Safadi F.F., Gorzelany I., Amin M., Popoff S.N., and Barbe M.F. Repetitive, negligible force reaching in rats induces pathological overloading of upper extremity bones. J. Bone. Miner. Res. 18 11 (2003) 2023-2032
52. Barr A.E., Barbe M.F., and Clark B.D. Systemic inflammatory mediators contribute to widespread effects in work-related musculoskeletal disorders. Exerc. Sport Sci. Rev. 32 4 (2004) 135-142
53. Al-Shatti T., Barr A.E., Safadi F.F., Amin M., and Barbe M.F. Increase in inflammatory cytokines in median nerves in a rat model of repetitive motion injury. J. Neuroimmunol. 167 1-2 (2005) 13-22
54. Barbe M.F., Elliott M.B., Abdelmagid S.M., Amin M., Popoff S.N., Safadi F.F., et al. Serum and tissue cytokines and chemokines increase with repetitive upper extremity tasks. J. Orthop. Res. 26 (2008) 1320-1326
55. Elliott M.B., Barr A.E., Kietrys D.M., Al-Shatti T., Amin M., and Barbe M.F. Peripheral neuritis and increased spinal cord neurochemicals are induced in a model of repetitive motion injury with low force and repetition exposure. Brain Res. 1218 (2008) 103-113
56. Zhu S., Barbe M.F., Amin N., Rani S., Popoff S.N., Safadi F.F., et al. Immunolocalization of Periostin-like factor and Periostin during embryogenesis. J. Histochem. Cytochem. 56 4 (2008) 329-345
57. Driban J.B., Barr A.E., Amin M., Sitler M.R., Ziskin M., Kendrick Z.V., et al. A novel model for inducing joint inflammation and degeneration with a pharmacological intervention to reduce its effects. Osteoarthritis and Cartilage (2008) Submitted
58. Chow J.W., Jagger C.J., and Chambers T.J. Characterization of osteogenic response to mechanical stimulation in cancellous bone of rat caudal vertebrae. Am. J. Physiol. 265 2 Pt 1 (1993) E340-E347
59. Chambers T.J., Evans M., Gardner T.N., Turner-Smith A., and Chow J.W. Induction of bone formation in rat tail vertebrae by mechanical loading. Bone. Miner. 20 2 (1993) 167-178
60. Wheeler D.L., Graves J.E., Miller G.J., Vander Griend R.E., Wronski T.J., Powers S.K., et al. Effects of running on the torsional strength, morphometry, and bone mass of the rat skeleton. Med. Sci. Sports Exerc. 27 4 (1995) 520-529
61. Barr A.E., and Barbe M.F. Pathophysiological tissue changes associated with repetitive movement: a review of the evidence. Phys. Ther. 82 2 (2002) 173-187 Review
62. Bourrin S., Palle S., Pupier R., Vico L., and Alexandre C. Effect of physical training on bone adaptation in three zones of the rat tibia. J. Bone. Miner. Res. 10 11 (1995) 1745-1752
63. Bourrin S., Genty C., Palle S., Gharib C., and Alexandre C. Adverse effects of strenuous exercise: a densitometric and histomorphometric study in the rat. J. Appl. Physiol. 76 5 (1994) 1999-2005
64. Maclean J.J., Lee C.R., Alini M., and Iatridis J.C. Anabolic and catabolic mRNA levels of the intervertebral disc vary with the magnitude and frequency of in vivo dynamic compression. J. Orthop. Res. 22 6 (2004) 1193-1200
65. Stokes I.A. Mechanical effects on skeletal growth. J. Musculoskelet. Neuronal. Interact. 2 3 (2002) 277-280
66. Stokes I.A., Clark K.C., Farnum C.E., and Aronsson D.D. Alterations in the growth plate associated with growth modulation by sustained compression or distraction. Bone 41 2 (2007) 197-205
67. Colopy S.A., Benz-Dean J., Barrett J.G., Sample S.J., Lu Y., Danova N.A., et al. Response of the osteocyte syncytium adjacent to and distant from linear microcracks during adaptation to cyclic fatigue loading. Bone 35 4 (2004) 881-891
68. Albrecht P.J., Thachara A., Vickers J., Barne M.F., Barr A.E., and Rice F.L. Alterations in cutaneous innervation and epidermal chemistry following repetitive motion injury in rats. Society for Neuroscience (2008) Poster Number 154.6