# TNF-α contributes to sarcopenia through caspase-8/caspase-3/GSDME-mediated pyroptosis

**Authors:** Jingying Wu, Siming Lin, Weixiao Chen, Guili Lian, Weibin Wu, Ai Chen, Mohammad Ismail Hajary Sagor, Li Luo, Huajun Wang, Liangdi Xie

PMC · DOI: 10.1038/s41420-023-01365-6 · 2023-02-24

## TL;DR

The paper shows that TNF-α causes sarcopenia by triggering a specific type of cell death called pyroptosis through a signaling pathway involving caspase-8, caspase-3, and GSDME.

## Contribution

The study reveals a novel mechanism linking TNF-α to sarcopenia via caspase-8/caspase-3/GSDME-mediated pyroptosis.

## Key findings

- TNF-α activates pyroptosis in myotubes through caspase-8 and caspase-3.
- TNF Complex IIb is more involved in activating caspase-8 and triggering pyroptosis.
- Pyroptosis leads to reduced MHC1 expression and loss of myotubes.

## Abstract

Sarcopenia has become a leading cause of disability and mortality in the elderly. It has been reported that programmed cell death (PCD) is associated with the development of sarcopenia that is characterized by reduction of muscle fiber size and number. TNF-α is also validated to play a prominent role in sarcopenia through its complex signaling pathways including cell death signaling. However, it is still unclear whether TNF-α contributes to sarcopenia by mediating pyroptosis, one type of PCD. Here, we first established naturally aged mice with sarcopenia model and confirmed an inflammatory state represented by TNF-α in aged mice. Evidence of GSDME-mediated pyroptosis and activation of apoptotic caspase-8/-3 were also found in skeletal muscle cells of aged mice with sarcopenia. We demonstrated that TNF-α triggered GSDME-mediated pyroptosis in myotubes through activating caspase-8 and caspase-3 by using caspase-8 and caspase-3 inhibitors. Comparing the activation of caspase-8 and GSDME expression between TNF Complex IIa and TNF Complex IIb, TNF-α was found to be more inclined to assemble TNF Complex IIb in activating caspase-8 and triggering pyroptosis. Moreover, pyroptotic myotubes were validated to result in decreased expression of MHC1 and finally loss of myotubes by knockdown of GSDME. Our work reveals a novel mechanism that TNF-ɑ/caspase-8/caspase-3/GSDME signaling-mediated pyroptosis contributes to the development of sarcopenia. Caspase-3/GSDME signaling-mediated pyroptosis may be a promising therapeutic target for sarcopenia.

## Linked entities

- **Genes:** GSDME (gasdermin E) [NCBI Gene 1687], Myo31DF (Myosin 31DF) [NCBI Gene 34445]
- **Proteins:** TNF (tumor necrosis factor), casp8 (caspase 8, apoptosis-related cysteine peptidase), Casp3 (caspase 3), GSDME (gasdermin E), Myo31DF (Myosin 31DF)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Atp9b (ATPase, class II, type 9B) [NCBI Gene 50771] {aka Atpc2b, IIb, MMR}, MYH4 (myosin heavy chain 4) [NCBI Gene 4622] {aka MYH2B, MyHC-2B, MyHC-IIb}, Pjvk (pejvakin) [NCBI Gene 381375] {aka Dfnb59, Gm1001}, MYH1 (myosin heavy chain 1) [NCBI Gene 4619] {aka HEL71, MYHSA1, MYHa, MyHC-2X/D, MyHC-2x}, Dntt (deoxynucleotidyltransferase, terminal) [NCBI Gene 21673] {aka Tdt}, Ripk1 (receptor (TNFRSF)-interacting serine-threonine kinase 1) [NCBI Gene 19766] {aka D330015H01Rik, RIP, RIP-1, Rinp, Rip1}, Gsdmc (gasdermin C) [NCBI Gene 83492] {aka Gsdmc1, Mlze}, Casp1 (caspase 1) [NCBI Gene 12362] {aka ICE, Il1bc}, Atp9a (ATPase, class II, type 9A) [NCBI Gene 11981] {aka IIa}, Gsdma (gasdermin A) [NCBI Gene 57911] {aka Gsdm, Gsdm1, Gsdma1, H312E}, Ripk3 (receptor-interacting serine-threonine kinase 3) [NCBI Gene 56532] {aka 2610528K09Rik, Rip3}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, Myh1 (myosin, heavy polypeptide 1, skeletal muscle, adult) [NCBI Gene 17879] {aka A530084A17Rik, IId, IId/x, MHC-2X/D, MHC2X/D, MYHC-IIX}, Crtap (cartilage associated protein) [NCBI Gene 56693] {aka 5730529N23Rik, CASP, Leprel3, P3h5}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Gsdmd (gasdermin D) [NCBI Gene 69146] {aka 1810036L03Rik, DF5L, Dfna5l, GsdmD-1, Gsdmdc1, M2-4}, Map3k7 (mitogen-activated protein kinase kinase kinase 7) [NCBI Gene 26409] {aka B430101B05, Tak1}, Tnfrsf1a (tumor necrosis factor receptor superfamily, member 1a) [NCBI Gene 21937] {aka CD120a, FPF, TNF-R, TNF-R-I, TNF-R1, TNF-R55}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Casp8 (caspase 8) [NCBI Gene 12370] {aka CASP-8, FLICE, MACH, Mch5}, caspase-8/-3 [NCBI Gene 12370;12367]
- **Diseases:** inflammation (MESH:D007249), loss of skeletal muscle mass (MESH:C536030), skeletal muscle damage (MESH:D005207), Sarcopenia (MESH:D055948), muscle damage (MESH:D009133), muscle fibers (MESH:C563545), GM (MESH:D019042), swelling (MESH:D004487), nuclear degeneration (MESH:D009410), GSDMD-N (MESH:C536108), PCD (MESH:D003643), cytotoxicity (MESH:D064420)
- **Chemicals:** phosphate (MESH:D010710), lipid (MESH:D008055), polyacrylamide (MESH:C016679), Tween (MESH:D011136), CO2 (MESH:D002245), hematoxylin (MESH:D006416), glutaraldehyde (MESH:D005976), Cycloheximide (MESH:D003513), DAPI (MESH:C007293), eosin (MESH:D004801), 5Z-7-Oxozeaenol (MESH:C505734), paraffin (MESH:D010232), GSK'872 (MESH:C000633405), PI (MESH:D010716), DMEM (-), nitrogen (MESH:D009584), Z-DEVD-FMK (MESH:C110772), HE (MESH:D006371), PBS (MESH:D007854), Z-IETD-FMK (MESH:C403753), uranyl acetate (MESH:C005460), water (MESH:D014867), DAB (MESH:C000469), hydrogen peroxide (MESH:D006861), Alexa Fluor 488 (MESH:C000711379), propidium iodide (MESH:D011419), TritonX-100 (MESH:D017830), Hoechst 33342 (MESH:C017807), paraformaldehyde (MESH:C003043), PVDF (MESH:C024865), Puromycin (MESH:D011691), sodium dodecyl sulfate (MESH:D012967)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** C2C12 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0188), C57/BL 6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), hU6 — Homo sapiens (Human), Finite cell line (CVCL_B0BH)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC9950087/full.md

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Source: https://tomesphere.com/paper/PMC9950087