# Exploring the Beneficial Effects of Se-Methylselenocysteine on GC-1/GC-2 Cells: From Cellular Uptake to Metabolic Pathway Regulation in Male Reproduction

**Authors:** Yiqing Lu, Xiaofei Duan, Huatao Che, Tong Li, Xiaoling Dun, Xinfa Wang, Lixi Jiang, Zhenna Chen, Hanzhong Wang

PMC · DOI: 10.3390/antiox15020270 · Antioxidants · 2026-02-22

## TL;DR

This study explores how Se-methylselenocysteine improves male reproductive cell health by boosting cell viability and regulating key metabolic pathways.

## Contribution

The study reveals novel insights into how MeSeCys enters cells and modulates metabolic pathways to support male reproductive health.

## Key findings

- MeSeCys significantly enhances the viability of GC-1 and GC-2 cells, with a stronger effect in GC-1 cells.
- MeSeCys increases intracellular selenium levels and glutathione metabolism in both cell lines.
- In GC-1 cells, MeSeCys modulates the mTOR pathway, influencing redox balance and glutathione metabolism.

## Abstract

Male infertility, a global health issue marked by spermatogenic failure, hinges on selenium (Se) as a key element for normal spermatogenesis. Among different Se species, Se-methylselenocysteine (MeSeCys) has been developed as a natural organic Se supplement with potent antioxidant and anti-inflammatory properties, but its direct effects on male reproduction need to be further explored. This study investigated the effect of MeSeCys on GC-1 spg (GC-1) and GC-2 spd (ts) (GC-2) cell lines, which mimic early stages. Treatment with 75 μmol/L MeSeCys for 24 h markedly enhanced the viability of both cell lines, with a more pronounced effect observed in GC-1 than in GC-2 cells. Moreover, this study demonstrated that MeSeCys enters cells through SLC7A11 or LRP8 channels and elevates intracellular Se levels in both GC-1 and GC-2 cells, with higher levels observed in GC-1 cells. RNA sequencing (RNA-seq) and bioinformatics analysis revealed that MeSeCys may regulate selenocompound metabolism and the glutathione metabolism pathway in both cell lines, increasing their intracellular glutathione (GSH) levels. Importantly, in GC-1 cells, MeSeCys specifically modulates the mTOR pathway, which further modulates glutathione metabolism and intracellular redox balance. This finding provides novel insights into the beneficial effects of MeSeCys on male reproductive cells, highlighting its potential as a nutritional supplement for male reproductive health.

## Linked entities

- **Genes:** SLC7A11 (solute carrier family 7 member 11) [NCBI Gene 23657], LRP8 (LDL receptor related protein 8) [NCBI Gene 7804], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475]
- **Chemicals:** Se-methylselenocysteine (PubChem CID 147004), glutathione (PubChem CID 124886), selenium (PubChem CID 6326970)
- **Diseases:** male infertility (MONDO:0005372)

## Full-text entities

- **Genes:** GSTA4 (glutathione S-transferase alpha 4) [NCBI Gene 2941] {aka GSTA4-4, GTA4}, Selenop (selenoprotein P) [NCBI Gene 20363] {aka D15Ucla1, Se-P, Sepp1, selp}, SLC3A2 (solute carrier family 3 member 2) [NCBI Gene 6520] {aka 4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1}, ATF4 (activating transcription factor 4) [NCBI Gene 468] {aka CREB-2, CREB2, TAXREB67, TXREB}, GSTP1 (glutathione S-transferase pi 1) [NCBI Gene 2950] {aka DFN7, FAEES3, GST3, GSTP, GSTP1-1, HEL-S-22}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, LRP8 (LDL receptor related protein 8) [NCBI Gene 7804] {aka APOER2, HSZ75190, LRP-8, MCI1}, Lrp8 (low density lipoprotein receptor-related protein 8, apolipoprotein e receptor) [NCBI Gene 16975] {aka 4932703M08Rik, ApoER2, Lr8b}, GSTM1 (glutathione S-transferase mu 1) [NCBI Gene 2944] {aka GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1}, Nfe2l2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 83619], SLC1A5 (solute carrier family 1 member 5) [NCBI Gene 6510] {aka AAAT, ASCT2, ATBO, M7V1, M7VS1, R16}, RPS6 (ribosomal protein S6) [NCBI Gene 6194] {aka S6, eS6}, GSS (glutathione synthetase) [NCBI Gene 2937] {aka CNSHA6, GSHS, HEL-S-64p, HEL-S-88n}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, GCLM (glutamate-cysteine ligase modifier subunit) [NCBI Gene 2730] {aka GLCLR}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, SEPHS2 (selenophosphate synthetase 2) [NCBI Gene 22928] {aka SPS2}, SLC7A11 (solute carrier family 7 member 11) [NCBI Gene 23657] {aka CCBR1, xCT}, Gpx4 (glutathione peroxidase 4) [NCBI Gene 29328] {aka Gshpx-4, Phgpx, gpx-4, snGpx}, Ephb1 (Eph receptor B1) [NCBI Gene 24338] {aka Ephb2, Erk, elk}, OLFM4 (olfactomedin 4) [NCBI Gene 10562] {aka GC1, GW112, OLM4, OlfD, UNQ362, bA209J19.1}, ORC1 (origin recognition complex subunit 1) [NCBI Gene 4998] {aka HSORC1, ORC1L, PARC1}, EIF4EBP1 (eukaryotic translation initiation factor 4E binding protein 1) [NCBI Gene 1978] {aka 4E-BP1, 4EBP1, BP-1, PHAS-I}, Slc7a11 (solute carrier family 7 (cationic amino acid transporter, y+ system), member 11) [NCBI Gene 26570] {aka 9930009M05Rik, sut, xCT}, GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729] {aka CNSHA7, GCL, GCS, GLCL, GLCLC}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}
- **Diseases:** spermatogenic failure (MESH:C562903), Infertility (MESH:D007246), endocrine disturbances (MESH:D004700), Cytotoxicity (MESH:D064420), abnormal spermatogenesis (MESH:C536875), cognitive deficits (MESH:D003072), Alzheimer's (MESH:D000544), lung carcinoma (MESH:D008175), cancer (MESH:D009369), injury to (MESH:D014947), inflammation (MESH:D007249), reproductive damage (MESH:D060737), genetic abnormalities (MESH:D030342), metabolic abnormalities (MESH:D008659), Male infertility (MESH:D007248)
- **Chemicals:** Na2SeO3 (MESH:D018038), amino acid (MESH:D000596), Se (MESH:D012643), H2O2 (MESH:D006861), CCK-8 (-), selenite (MESH:D020887), cystine (MESH:D003553), SeMet (MESH:D012645), BSO (MESH:D019328), PBS (MESH:D007854), arsenic (MESH:D001151), Cd (MESH:D002104), nitric acid (MESH:D017942), ROS (MESH:D017382), SeCys (MESH:D017279), GSH (MESH:D005978), lipid (MESH:D008055), rapamycin (MESH:D020123), selenocystine (MESH:C009226), zinc (MESH:D015032), 5-ethynyl-2'-deoxyuridine (MESH:C031086), DEHP (MESH:D004051), sorafenib (MESH:D000077157), E (MESH:D004540), water (MESH:D014867), testosterone (MESH:D013739), MeSeCys (MESH:C002979)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Allium cepa (onion, species) [taxon 4679], Capra hircus (domestic goat, species) [taxon 9925], Brassica oleracea var. italica (asparagus broccoli, varietas) [taxon 36774], Mus musculus (house mouse, species) [taxon 10090], Candida albicans (species) [taxon 5476], Allium sativum (garlic, species) [taxon 4682]
- **Cell lines:** GC-1 — Homo sapiens (Human), Transformed cell line (CVCL_6632), 1E — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_L871), GC-2 — Mus musculus (Mouse), Conditionally immortalized cell line (CVCL_6633), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937993/full.md

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Source: https://tomesphere.com/paper/PMC12937993