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Record W2024565857 · doi:10.1055/s-0032-1319991

Effect of Parathyroid Hormone on MAPK Signaling and Calcification Markers in Human Intervertebral Disk Cells

2012· article· en· W2024565857 on OpenAlexaff
Padma Madiraju, Rahul Gawri, John Antoniou, F. Mwale

Bibliographic record

VenueGlobal Spine Journal · 2012
Typearticle
Languageen
FieldMedicine
TopicSpine and Intervertebral Disc Pathology
Canadian institutionsMcGill UniversityJewish General Hospital
Fundersnot available
KeywordsAlkaline phosphataseParathyroid hormoneCalcificationMedicineMesenchymal stem cellEndochondral ossificationIntervertebral discInternal medicineEndocrinologyChondrogenesisCalciumMolecular biologyPathologyChemistryCartilageBiologyAnatomyBiochemistryEnzyme

Abstract

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Introduction Back pain is strongly associated with degeneration of the intervertebral disk (IVD), which is associated with ongoing mineral deposition. 1 The presence of calcium deposits and type X collagen (COL X) and the level of the indicators of calcification potential (alkaline phosphatase (ALP), Ca 2 + ions and Pi) were consistently higher in degenerative and scoliotic discs. We also showed that in mesenchymal stem cells (MSCs), parathyroid hormone (PTH 1–34) inhibits the expression of COL X while promoting type II collagen (COL II) expression, thereby preventing endochondral ossification. 2 In this study, we investigated the effect of PTH on expression of COLII, COLX, and ALP in human IVD cells and analyzed the potential mechanisms related to its effect. Materials and Methods Human lumbar IVDs from a donor without spinal pathology were obtained within 24 hours after death. Nucleus pulposus (NP) and annulus fibrosus (AF) tissues from the IVDs were digested and the corresponding NP and AF primary cells were isolated as previously described. 3 These cells were cultured in complete DMEM to 90% confluence. Then the cells were incubated overnight in serum-free medium followed by treatment with 100 nM PTH 30 minutes to 48 hours. Protein expression was analyzed by immunoblotting using specific antibodies to COL I and COL II (Abcam, Cambridge, MA), COL X, and PTH receptor 1 (Sigma Aldrich). Expression and phosphorylation of AKT and MAPKs was assessed by using specific corresponding antibodies (Cell Signaling, Danvers, MA). Alkaline phosphatase activity was measured colorimetrically using the StemTAG kit (Cell Biolabs, San Diego, CA, USA) and Ca 2 + release from cells was measured using calcium assay kit (Cayman Chemical, Ann Arbor, MI, USA). Statistical analyses were done using one-way ANOVA, posthoc tests p < 0.05 was considered significant. Results Effect of PTH on PTH receptor 1 We confirmed the presence of PTH receptor 1 on the AF and NP cells and showed the effect of PTH on the PTH receptor 1 activation by incubating AF and NP cells with 100 nM PTH (1–34). Effect of PTH on collagen expression PTH increased the expression of COL-II significantly in AF cells after 6 hours of incubation and in NP cells COL-II expression increased in a time-dependent and sustained manner from 6 to 48 hours of incubation. Expression of COL-X was not altered by PTH in AF cells, whereas in NP cells it decreased significantly from 6 to 48 hours. Effect of PTH on MAPK signaling PTH causes ERK activation by phosphorylation within 30 minutes both in AF and NP cells (Fig. 1). PTH stimulated ERK phosphorylation was found to be sustained up to 6 hours followed by a slow decrease (Fig. 1). However, PTH led to JNK phosphorylation within 30 minutes of incubation and this declined thereafter over 48 hours. PTH stimulation of p38 MAPK phosphorylation was not altered in AF cells, whereas in NP cells there was a significant activation of p38 at 30 minutes by PTH. There was a decline in p38 phosphorylation below the control levels after 24 hours of incubation with PTH. Effect of PTH on AKT signaling Results show that PTH causes AKT ( ser 473) activation by phosphorylation at 1 hour in NP cells and has no effect in AF cells. Effect of PTH on Calcification markers The activity of alkaline phosphatase was significantly decreased by PTH after 24 hours of incubation in NP cells. In AF cells, no significant changes were observed, even though there was a trend to increase at 48 hours. PTH significantly increased calcium release into the medium at 48 hours in NP cells and no significant change was observed in AF cells Conclusion PTH has previously been shown to promote chondrogenesis and to inhibit the expression of COL-X in chondrocytes probably via the activation of MAPK signaling pathways. 4 The present results demonstrate that PTH upregulates COL-II and downregulates COL-X in IVD cells, indicating that PTH has the potential of being able to stimulate disk repair and to improve nutrient supply in the degenerative disc. Our data also suggests that activation of MAPK pathway takes place much earlier than the alterations in COL-II or COL-X expression. Interestingly, COL-II expression inversely correlates with alkaline phosphatase activity in NP cells treated with PTH. Although understanding of IVD calcification would be of great value, not only for elucidation of its mechanism, but with an eye toward eventual therapeutic intervention. PTH can thus be used towards disk regeneration therapy. I confirm having declared any potential conflict of interest for all authors listed on this abstract Yes Disclosure of Interest None declared Hristova, GI et al. Journal of Orthopaedic Research 2011; epub Mwale F et al. Tissue Engeneering Part A (2010)16:3449–3455 Chelberg MK et al. Journal of Anatomy 1995;186 (Pt 1): 43–53 Datta, NS et al. Cell Signalling 2010;22: 457–46

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.013
GPT teacher head0.318
Teacher spread0.305 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2012
Admission routes1
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