Effect of calcitriol and calcium on basal ganglia calcification in hypoparathyroidism: experimental models

in Journal of Molecular Endocrinology
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Parmita KarDepartment of Endocrinology and Metabolism, All India Institute of Medical Sciences, New Delhi, India

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Ravinder GoswamiDepartment of Endocrinology and Metabolism, All India Institute of Medical Sciences, New Delhi, India

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Correspondence should be addressed to R Goswami or P Kar: gosravinder@aiims.edu or parmitakar27@gmail.com
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Basal ganglia calcification (BGC) is a common complication in hypoparathyroid patients, linked to hyperphosphatemia and altered vitamin-D and calcium homeostasis following conventional therapy. The pathogenesis of BGC in hypoparathyroidism is not clear. Recently, we developed an ex vivo model of BGC using rat-striatal cell culture in 10.0 mmol/L of β-glycerophosphate (31.8 mg/dL phosphate). However, the effect of 1,25(OH)2 D, calcium, and milder phosphate excess on BGC in hypoparathyroidism is not known. This study describes two modified ex vivo models investigating pathogenesis of BGC in ‘drug-naïve’ and ‘conventionally treated’ hypoparathyroid state. The first modification involved striatal cells cultured in low concentration 1,25(OH)2D (16.0 pg/mL), ionized calcium(0.99 mmol/L), hPTH(1-34) (6.0 pg/mL), and 2.68 mmol/L (8.3 mg/dL) of phosphate akin to ‘drug-naïve’ state for 24 days. In second modification, striatal cells were exposed to 46.0 pg/mL of 1,25(OH)2D, normal ionized calcium of 1.17 mmol/L, and 2.20 mmol/L (6.8 mg/dL) of phosphate akin to ‘conventionally treated’ state. Striatal cell culture under ‘drug-naïve’ state showed that even 16.0 pg/mL of 1,25(OH)2D enhanced the calcification. In ‘conventionally treated’ model, striatal cell calcification was enhanced in 54% cases over ‘drug-naïve’ state. Calcification in ‘conventionally treated’ state further increased on increasing phosphate to 8.3 mg/dL, suggesting importance of phosphatemic control in hypoparathyroid patients. Striatal cells in ‘drug-naïve’ state showed increased mRNA expression of pro-osteogenic Wnt3a, Cd133,Vglut-1-neuronal phosphate-transporters, calcium-ion channel-Trvp2,Alp, and Collagen-1α and decreased expression of Ca-II. These models suggest that in ‘drug-naïve’ state, 1,25(OH)2D along with moderately elevated phosphate increases the expression of pro-osteogenic molecules to induce BGC. Although normalization of calcium in ‘conventionally treated’ state increased the expression of Opg, Osterix, Alp, and Cav2, calcification increased only in a subset, akin to variation in progression of BGC in hypoparathyroid patients on conventional therapy.

 

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  • Aggarwal S, Kailash S, Sagar R, Tripathi M, Sreenivas V, Sharma R, Gupta N & Goswami R 2013 Neuropsychological dysfunction in idiopathic hypoparathyroidism and its relationship with intracranial calcification and serum total calcium. European Journal of Endocrinology 168 895903. (https://doi.org/10.1530/EJE-12-0946)

    • Search Google Scholar
    • Export Citation
  • Fretz JA, Zella LA, Kim S, Shevde NK & Pike JW 2007 1,25-Dihydroxyvitamin D3 induces expression of the Wnt signaling co-regulator LRP5 via regulatory elements located significantly downstream of the gene’s transcriptional start site. Journal of Steroid Biochemistry and Molecular Biology 103 440445. (https://doi.org/10.1016/j.jsbmb.2006.11.018)

    • Search Google Scholar
    • Export Citation
  • Gafni RI & Collins MT 2019 Hypoparathyroidism. New England Journal of Medicine 380 17381747. (https://doi.org/10.1056/NEJMcp1800213)

  • Goswami R, Millo T, Mishra S, Das M, Kapoor M, Tomar N, Saha S, Roy TS & Sreenivas V 2014 Expression of osteogenic molecules in the caudate nucleus and gray matter and their potential relevance for Basal Ganglia calcification in hypoparathyroidism. Journal of Clinical Endocrinology and Metabolism 99 17411748. (https://doi.org/10.1210/jc.2013-3863)

    • Search Google Scholar
    • Export Citation
  • Goswami R, Sharma R, Sreenivas V, Gupta N, Ganapathy A & Das S 2012 Prevalence and progression of basal ganglia calcification and its pathogenic mechanism in patients with idiopathic hypoparathyroidism. Clinical Endocrinology 77 200206. (https://doi.org/10.1111/j.1365-2265.2012.04353.x)

    • Search Google Scholar
    • Export Citation
  • Haussler MR, Haussler CA, Whitfield GK, Hsieh JC, Thompson PD, Barthel TK, Bartik L, Egan JB, Wu Y & Kubicek JL et al.2010 The nuclear vitamin D receptor controls the expression of genes encoding factors which feed the ‘Fountain of Youth' to mediate healthful aging. Journal of Steroid Biochemistry and Molecular Biology 121 8897. (https://doi.org/10.1016/j.jsbmb.2010.03.019)

    • Search Google Scholar
    • Export Citation
  • Jensen N, Schrøder HD, Hejbøl EK, Füchtbauer EM, de Oliveira JR & Pedersen L 2013 Loss of function of Slc20a2 associated with familial idiopathic Basal Ganglia calcification in humans causes brain calcifications in mice. Journal of Molecular Neuroscience 51 994999. (https://doi.org/10.1007/s12031-013-0085-6)

    • Search Google Scholar
    • Export Citation
  • Kar P, Millo T, Saha S, Mahtab S, Agarwal S & Goswami R 2021 Osteogenic Mechanisms of Basal Ganglia Calcification and its ex vivo Model in the Hypoparathyroid milieu. Endocrinology 162 bqab024. (https://doi.org/10.1210/endocr/bqab024)

    • Search Google Scholar
    • Export Citation
  • Legati A, Giovannini D, Nicolas G, López-Sánchez U, Quintáns B, Oliveira JR, Sears RL, Ramos EM, Spiteri E & Sobrido MJ et al.2015 Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export. Nature Genetics 47 579581 (https://doi.org/10.1038/ng.3289)

    • Search Google Scholar
    • Export Citation
  • Livak KJ & Schmittgen TD 2001 Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25 402408 (https://doi.org/10.1006/meth.2001.1262)

    • Search Google Scholar
    • Export Citation
  • Lund B, Sørensen OH, Lund B, Bishop JE & Norman AW 1980 Vitamin D metabolism in hypoparathyroidism. Journal of Clinical Endocrinology and Metabolism 51 606610 (https://doi.org/10.1210/jcem-51-3-606)

    • Search Google Scholar
    • Export Citation
  • Markowitz ME, Rosen JF, Smith C & DeLuca HF 1982 1,25-Dihydroxyvitamin D3-treated hypoparathyroidism: 35 patients years in 10 children. Journal of Clinical Endocrinology and Metabolism 55 727733. (https://doi.org/10.1210/jcem-55-4-727)

    • Search Google Scholar
    • Export Citation
  • Pálmer HG, Anjos-Afonso F, Carmeliet G, Takeda H & Watt FM 2008 The vitamin D receptor is a Wnt effector that controls hair follicle differentiation and specifies tumor type in adult epidermis. PLoS One 3 e1483. (https://doi.org/10.1371/journal.pone.0001483)

    • Search Google Scholar
    • Export Citation
  • Pereira S, Veeraraghavan P, Ghosh S & Gandhi M 2004 Animal experimentation and ethics in India: the CPCSEA makes a difference. Alternatives to Laboratory Animals 32(Supplement 1B) 411415. (https://doi.org/10.1177/026119290403201s67)

    • Search Google Scholar
    • Export Citation
  • Saha S & Goswami R 2019 Auditing the efficacy and safety of alfacalcidol and calcium therapy in idiopathic hypoparathyroidism. Journal of Clinical Endocrinology and Metabolism 104 13251335. (https://doi.org/10.1210/jc.2018-02228)

    • Search Google Scholar
    • Export Citation
  • Sugimoto T, Nakada M, Fukase M, Imai Y, Kinoshita Y & Fujita T 1986 Effects of ascorbic acid on alkaline phosphatase activity and hormone responsiveness in the osteoblastic osteosarcoma cell line UMR-106. Calcified Tissue International 39 171174 (https://doi.org/10.1007/BF02555114)

    • Search Google Scholar
    • Export Citation
  • Walsh S, Jordan GR, Jefferiss C, Stewart K & Beresford JN 2001 High concentrations of dexamethasone suppress the proliferation but not the differentiation or further maturation of human osteoblast precursors in vitro: relevance to glucocorticoid-induced osteoporosis. Rheumatology 40 7483 (https://doi.org/10.1093/rheumatology/40.1.74)

    • Search Google Scholar
    • Export Citation
  • Wang J, Zhou JJ, Robertson GR & Lee VW 2018 Vitamin D in vascular calcification: a double-edged sword? Nutrients 10 652 (https://doi.org/10.3390/nu10050652)

    • Search Google Scholar
    • Export Citation
  • Zanatta L, Goulart PB, Gonçalves R, Pierozan P, Winkelmann-Duarte EC, Woehl VM, Pessoa-Pureur R, Silva FR & Zamoner A 2012 1α,25-Dihydroxyvitamin D(3) mechanism of action: modulation of L-type calcium channels leading to calcium uptake and intermediate filament phosphorylation in cerebral cortex of young rats. Biochimica et Biophysica Acta 1823 17081719. (https://doi.org/10.1016/j.bbamcr.2012.06.023)

    • Search Google Scholar
    • Export Citation