# Ribosome heterogeneity and specialization in musculoskeletal physiology and pathology

**Authors:** Alzbeta Chabronova, Guus G H van den Akker, Tim J M Welting, Mandy J Peffers

PMC · DOI: 10.1093/jbmrpl/ziag018 · JBMR Plus · 2026-02-02

## TL;DR

This review explores how ribosome diversity and specialization influence musculoskeletal health and disease, highlighting their potential as new therapeutic targets.

## Contribution

The paper introduces ribosome heterogeneity and specialization as emerging concepts with significant implications for musculoskeletal biology and pathology.

## Key findings

- Ribosome heterogeneity supports development and homeostasis in musculoskeletal tissues.
- Specialized ribosomes contribute to both normal tissue function and disease progression.
- New technologies are enabling deeper understanding of ribosome roles in MSK biology.

## Abstract

Musculoskeletal (MSK) tissues are highly dynamic systems that rely on tightly regulated protein synthesis to maintain homeostasis and structural integrity, adapt to physiological stimuli, and respond to injury. The deregulation of protein synthesis is implicated in a wide range of MSK pathologies. At the core of protein synthesis are ribosomes, complex molecular nanomachines that translate mRNAs and generate proteins. Once considered uniform entities passively exerting their function, ribosomes are now recognized to be heterogeneous in their composition and capable of specialized functions. These emerging concepts of ribosome heterogeneity and specialization are increasingly recognized as key regulators of physiological and pathological cellular processes across fields. Although the MSK field has yet to fully embrace and integrate ribosome-centered research, accumulating evidence suggests that ribosome heterogeneity and specialization might have profound implications for MSK (patho)biology. In this review, we summarize the emerging data across MSK tissues (bone, skeletal muscle, articular cartilage, tendons, and ligaments), highlighting the roles of ribosomes in supporting development, maintaining homeostasis, and facilitating cellular and tissue functions and adaptations, but also driving pathological changes and disease progression. Furthermore, we also outline recent key technological and methodological advances that are critical for uncovering the full scope, significance, and dynamic regulation of ribosome heterogeneity and specialization in MSK (patho)biology. As the field moves forward, ribosome-centered research holds great promise in revealing new mechanisms underlying MSK biology and identifying novel therapeutic targets.

Graphical Abstract

## Full-text entities

- **Genes:** RPL7A (60S ribosomal protein uL30 RPL7A) [NCBI Gene 852804], Runx1 (runt related transcription factor 1) [NCBI Gene 12394] {aka AML1, CBF-alpha-2, Cbfa2, Pebp2a2, Pebpa2b}, Acan (aggrecan) [NCBI Gene 11595] {aka Agc, Agc1, CSPCP, Cspg1, b2b183Clo, cmd}, Rps27l (ribosomal protein S27-like) [NCBI Gene 67941] {aka 1810034D23Rik}, Rps15 (ribosomal protein S15) [NCBI Gene 20054] {aka rig}, Hspa1a (heat shock protein family A (Hsp70) member 1A) [NCBI Gene 193740] {aka Hsp70-3, Hsp70.3, Hsp72, hsp68, hsp70A1}, Rpl38 (ribosomal protein L38) [NCBI Gene 67671] {aka 0610025G13Rik, Rbt, Ts, Tss}, Apobec3 (apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3) [NCBI Gene 80287] {aka Apobec, Arp3, Cem15, Gm20117, Rfv3}, Lef1 (lymphoid enhancer binding factor 1) [NCBI Gene 16842] {aka 3000002B05, Lef-1}, SRSF4 (serine and arginine rich splicing factor 4) [NCBI Gene 6429] {aka SFRS4, SRP75}, RPL7B (60S ribosomal protein uL30 RPL7B) [NCBI Gene 855903], Rpl35 (ribosomal protein L35) [NCBI Gene 66489] {aka 2410039E09Rik}, Fgf2 (fibroblast growth factor 2) [NCBI Gene 14173] {aka Fgf-2, Fgf2a, Fgfb, bFGF}, Rps6 (ribosomal protein S6) [NCBI Gene 20104] {aka S6R}, Dhx30 (DExH-box helicase 30) [NCBI Gene 72831] {aka 2810477H02Rik, C130058C04Rik, Ddx30, HELG, Ret-CoR}, Snora33 (small nucleolar RNA, H/ACA box 33) [NCBI Gene 100529074] {aka ACA33, MBI-42}, Rpl10a (ribosomal protein L10A) [NCBI Gene 19896] {aka CsA-19, Nedd6}, Myc (Myc proto-oncogene, bHLH transcription factor) [NCBI Gene 17869] {aka Myc2, Niard, Nird, bHLHe39}, BMP7 (bone morphogenetic protein 7) [NCBI Gene 655] {aka OP-1}, RPS3 (ribosomal protein S3) [NCBI Gene 6188] {aka S3, uS3}, Fbl (fibrillarin) [NCBI Gene 14113] {aka FIB, FLRN, RNU3IP1}, Trp53-ps (transformation related protein 53, pseudogene) [NCBI Gene 22060], Ctsl (cathepsin L) [NCBI Gene 13039] {aka 1190035F06Rik, CatL, Ctsl1, MEP, fs, nkt}, Igf1r (insulin-like growth factor I receptor) [NCBI Gene 16001] {aka A330103N21Rik, CD221, D930020L01, IGF-1R, hyft}, FBL (fibrillarin rRNA 2'-O-methyltransferase) [NCBI Gene 2091] {aka FIB, FLRN, Nop1, RNU3IP1}, RLP7 (Rlp7p) [NCBI Gene 855730] {aka RPL7}, Pkm (pyruvate kinase, muscle) [NCBI Gene 18746] {aka Pk-2, Pk-3, Pk3, Pkm2}, Mmp13 (matrix metallopeptidase 13) [NCBI Gene 17386] {aka Clg, MMP-13, Mmp1}, Es28 (esterase 28) [NCBI Gene 109612] {aka Es-28}, RPL22L1 (ribosomal protein L22 like 1) [NCBI Gene 200916], RPS20 (ribosomal protein S20) [NCBI Gene 6224] {aka S20, uS10}, Fn1 (fibronectin 1) [NCBI Gene 14268] {aka E330027I09, Fn, Fn-1}, EIF4A3 (eukaryotic translation initiation factor 4A3) [NCBI Gene 9775] {aka DDX48, Fal1, MUK34, NMP265, NUK34, RCPS}, Col1a1 (collagen, type I, alpha 1) [NCBI Gene 12842] {aka Col1a-1, Cola-1, Cola1, Mov-13, Mov13}, Rn28s1 (28S ribosomal RNA) [NCBI Gene 236598] {aka 28s}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Rpl39l (ribosomal protein L39-like) [NCBI Gene 68172] {aka 4930517K11Rik}, Snord82 (small nucleolar RNA, C/D box 82) [NCBI Gene 80828] {aka Rnu82, U82, Z25}, Rps28 (ribosomal protein S28) [NCBI Gene 54127], Es6 (esterase 6) [NCBI Gene 109581] {aka Es-6}, Rpl3 (ribosomal protein L3) [NCBI Gene 27367] {aka F2, J1}, Snora7a (small nucleolar RNA, H/ACA box 7A) [NCBI Gene 100217451] {aka MBI-141}, Rapsn (receptor-associated protein of the synapse) [NCBI Gene 19400] {aka 43kDa, Nraps, Raps, rapsyn}, Rpl3l (ribosomal protein L3-like) [NCBI Gene 66211] {aka 1110057H16Rik}, Runx2 (runt related transcription factor 2) [NCBI Gene 12393] {aka AML3, CBF-alpha-1, Cbf, Cbfa-1, Cbfa1, LS3}, Lrpap1 (low density lipoprotein receptor-related protein associated protein 1) [NCBI Gene 16976] {aka HBP44, RAP}, Ccl7 (C-C motif chemokine ligand 7) [NCBI Gene 20306] {aka MCP-3, Scya7, fic, marc, mcp3}, Cd24a (CD24a antigen) [NCBI Gene 12484] {aka Cd24, HSA, Ly-52, nectadrin}, RPS10 (ribosomal protein S10) [NCBI Gene 6204] {aka DBA9, S10, eS10}, Dkc1 (dyskeratosis congenita 1, dyskerin) [NCBI Gene 245474], Fau (FAU ubiquitin like and ribosomal protein S30 fusion) [NCBI Gene 14109] {aka MNSFB, MNSFbeta}, Pdcd11 (programmed cell death 11) [NCBI Gene 18572] {aka 1110021I22Rik, ALG-4, Pdcd7, mKIAA0185}, EIF4A2 (eukaryotic translation initiation factor 4A2) [NCBI Gene 1974] {aka BM-010, DDX2B, EIF4A, EIF4F, NEDHSS, eIF-4A-II}, Sox9 (SRY (sex determining region Y)-box 9) [NCBI Gene 20682] {aka 2010306G03Rik, mKIAA4243, mSox9}, Rps26 (ribosomal protein S26) [NCBI Gene 27370], Rmrp (RNA component of mitochondrial RNAase P) [NCBI Gene 19782] {aka 1110032O22Rik, Rmrpr}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, MRPS15 (mitochondrial ribosomal protein S15) [NCBI Gene 64960] {aka DC37, MPR-S15, RPMS15, S15mt, uS15m}, TGFB2 (transforming growth factor beta 2) [NCBI Gene 7042] {aka CAEND2, G-TSF, LDS4, TGF-beta2}
- **Diseases:** genetic disorders (MESH:D030342), OA (MESH:D010003), acute myeloid leukemia (MESH:D015470), BMD (MESH:D020388), hypoxia (MESH:D000860), cartilage damage (MESH:D002357), muscle mass (MESH:C536030), bone marrow failure (MESH:D000080983), GBM (MESH:D005909), hypoxic (MESH:D002534), osteopenia (MESH:D001851), MSK diseases (MESH:D009140), fatigue (MESH:D005221), Cancer (MESH:D009369), hypertrophy (MESH:D006984), end-stage OA (MESH:D007676), limb malformations (MESH:C535856), muscle weakness and degeneration (MESH:D018908), dilated cardiomyopathy (MESH:D002311), RPs (MESH:D011488), osteoporotic (MESH:D058866), atrophy (MESH:D001284), osteoporosis (MESH:D010024), osteogenesis imperfecta (MESH:D010013), craniofacial defects (MESH:D019465), glioma (MESH:D005910), sarcopenia (MESH:D055948), muscle atrophy (MESH:D009133), inflammation (MESH:D007249), degenerative joint disorder (MESH:D019636), short stature (MESH:D006130), skeletal muscle hypertrophy (MESH:C536106), leukemia (MESH:D007938), muscle (MESH:D019042), cardiac muscle contraction (MESH:C536214)
- **Chemicals:** poly-lysine (MESH:D011107), ribose (MESH:D012266), U14 (MESH:C015293), ATP (MESH:D000255), water (MESH:D014867), sulfhydryl (MESH:D013438), rapamycin (MESH:D020123), N6-methyladenosine (MESH:C010223), 2'-O-me (-), O (MESH:D010100)
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227], Vibrio vulnificus (species) [taxon 672], Equus caballus (domestic horse, species) [taxon 9796], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Danio rerio (leopard danio, species) [taxon 7955], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** SW1353 — Homo sapiens (Human), Primary central chondrosarcoma, Cancer cell line (CVCL_0543), mATDC5 — Mus musculus (Mouse), Transformed cell line (CVCL_5U93), MG1655 — Homo sapiens (Human), Maple syrup urine disease, Transformed cell line (CVCL_D514), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), Mov-13 — Mus musculus (Mouse), Hybridoma (CVCL_LH59), MC3T3-E1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0409), C2C12 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0188), HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), hESCs — Homo sapiens (Human), Embryonic stem cell (CVCL_UI95)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12931454/full.md

## References

229 references — full list in the complete paper: https://tomesphere.com/paper/PMC12931454/full.md

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Source: https://tomesphere.com/paper/PMC12931454