mtDNA haplogroup J Modulates telomere length and Nitric Oxide production
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- 作者：Mercedes Fernández-Moreno (1)
María Tamayo (2)
Angel Soto-Hermida (1)
Alejandro Mosquera (2)
Natividad Oreiro (1)
Carlos Fernández-López (1)
José Luis Fernández (2)
Ignacio Rego-Pérez (1)
Francisco J Blanco (1) (3) (4) - 关键词：mitochondria ; osteoarthritis ; cartilage ; arthritis ; nitric oxide ; telomere
- 刊名：BMC Musculoskeletal Disorders
- 出版年：2011
- 出版时间：December 2011
- 年：2011
- 卷：12
- 期：1
- 全文大小：330KB
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44. The pre-publication history for this paper can be accessed here:l.com/1471-2474/12/283/prepub" class="a-plus-plus">http://www.biomedcentral.com/1471-2474/12/283/prepub - 作者单位：Mercedes Fernández-Moreno (1)
María Tamayo (2)
Angel Soto-Hermida (1)
Alejandro Mosquera (2)
Natividad Oreiro (1)
Carlos Fernández-López (1)
José Luis Fernández (2)
Ignacio Rego-Pérez (1)
Francisco J Blanco (1) (3) (4)
1. Rheumatology Division, INIBIC-Complejo Hospitalario Universitario A Coru?a (CHUAC), As Xubias 84, 15006-A, Coru?a, Spain
2. Genetics Unit, INIBIC-Complejo Hospitalario Universitario A Coru?a (CHUAC), As Xubias 84, 15006-A, Coru?a, Spain
3. Proteo-Red/ISCIII, Madrid, Spain
4. CIBER-BBN-ISCIII, Madrid, Spain
文摘
Background Oxidative stress due to the overproduction of nitric oxide (NO) and other oxygen reactive species (ROS), play a main role in the initiation and progression of the OA disease and leads to the degeneration of mitochondria. Therefore, the goal of this work is to describe the difference in telomere length of peripheral blood leukocytes (PBLs) and Nitric Oxide (NO) production between mitochondrial DNA (mtDNA) haplogroup J and non-J carriers, as indirect approaches of oxidative stress. Methods The telomere length of PBL was analyzed in DNA samples from 166 healthy controls (114 J and 52 non-J) and 79 OA patients (41 J and 38 non-J) by means of a validated qPCR method. The NO production was assessed in 7 carriers of the haplogroup J and 27 non-J carriers, by means of the colorimetric reaction of the Griess reagent in supernatants of cultured chondrocytes. Inducible nitric oxide synthase (iNOS) mRNA from these samples was analyzed by qPCR. Appropiated statistical analyses were performed Results Carriers of the haplogroup J showed a significantly longer telomere length of PBLs than non-J carriers, regardless of age, gender and diagnosis (p = 0.025). Cultured chondrocytes carrying the mtDNA haplogroup J also showed a lower NO production than non-J carriers (p = 0.043). No significant correlations between age and telomore length of PBLs were detected neither for carriers of the haplogroup J nor for non-J carriers. A strong positive correlation between NO production and iNOS expression was also observed (correlation coefficient = 0.791, p < 0.001). Conclusion The protective effect of the mtDNA haplogroup J in the OA disease arise from a lower oxidative stress in carriers of this haplogroup, since this haplogroup is related to lower NO production and hence longer telomere length of PBLs too.