# Skin bacteriota ameliorates androgenetic alopecia via harmonizing skin immuno inflammatory balance

**Authors:** Yichen Cao, Xusheng Wu, Zixuan Huang, Chen Xu, Zengyan Ge, Yixin Xie, Lan Wu, Ying Qian, Bin Ding, Hongbin Luo

PMC · DOI: 10.1007/s42770-026-01911-1 · 2026-03-18

## TL;DR

This study shows that skin bacteria can help reduce hair loss in mice by balancing skin inflammation.

## Contribution

The study identifies specific bacteria that may help treat androgenetic alopecia by modulating inflammation.

## Key findings

- Restoring skin bacteriota improves hair growth in AGA model mice.
- Lactobacillus and Proteus may influence immuno-inflammatory balance.
- Modulation of TLR4/NF-κB pathways is linked to reduced inflammation and hair loss.

## Abstract

The human skin is the largest heterogeneous organ that protects the body from pathogens such as bacteria, fungi, mites, and viruses. The coexistence of skin microorganisms associated with the host helps maintain tissue integrity and immune homeostasis. This study aimed to investigate the effect of the skin microbiome on hair growth in androgenic alopecia (AGA) model mice. The dihydrotestosterone induced AGA model mice were engaged in this study. The ABF (Antibiotic-Free) and ABT (Antibiotic-Treated) mice were topically administrated with ddH2O and antibiotics, respectively. Seven days later, the three of mice in the ABF and ABT group were co-housed. Compared to ABF mice, ABT mice exhibited sparse hair, thinner skin, and fewer hair follicles, all of which has been improved in the Co-housed ABF/ABT mice. The translational expression of β-catenin and Wnt5a, as well as the mRNA levels of Vegfa, Fgfr, Igf1, and Lef1 decreased in ABT mice but recovered in ABF/ABT mice. Increased the expression of TLR4 and NF-κB, IL-6, and the mRNA levels of Il-17 levels in ABT mice compared to ABF mice indicated inflammation in dorsal skin. Cohousing notably affected Il-6, Il-17, Il-23, and Tnfα levels. The 16S rDNA sequencing results and the correlative analysis indicated that the relative abundance of Lactobacillus and Proteus might be the key genus influencing the immuno-inflammatory balance. Our findings suggest that restoring the dorsal skin bacteriota promotes hair growth in AGA model mice. This improvement is likely mediated by the modulation of the skin’s inflammatory microenvironment. Importance. This study highlights the critical role of skin bacteriota in modulating immuno-inflammatory balance in AGA, suggesting that restoration of bacteriota may contribute to the amelioration of DHT-induced hair loss by regulating TLR4/NF-κB pathways, which offers a novel insight for bacterial -based therapies.

The online version contains supplementary material available at 10.1007/s42770-026-01911-1.

## Linked entities

- **Genes:** ctnnb1.S (catenin beta 1 S homeolog) [NCBI Gene 380441], WNT5A (Wnt family member 5A) [NCBI Gene 7474], VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422], FGFR (fibroblast growth factor receptor) [NCBI Gene 373310], IGF1 (insulin like growth factor 1) [NCBI Gene 3479], LEF1 (lymphoid enhancer binding factor 1) [NCBI Gene 51176], TLR4 (toll like receptor 4) [NCBI Gene 7099], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], IL6 (interleukin 6) [NCBI Gene 3569], IL17A (interleukin 17A) [NCBI Gene 3605], IL37 (interleukin 37) [NCBI Gene 27178], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Chemicals:** dihydrotestosterone (PubChem CID 10635)
- **Diseases:** androgenetic alopecia (MONDO:0005339)

## Full-text entities

- **Genes:** Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Il23a (interleukin 23, alpha subunit p19) [NCBI Gene 83430] {aka IL-23, p19}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Igf1 (insulin-like growth factor 1) [NCBI Gene 16000] {aka C730016P09Rik, Igf-1, Igf-I}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Wnt5a (wingless-type MMTV integration site family, member 5A) [NCBI Gene 22418] {aka 8030457G12Rik, Wnt-5a}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, Slc17a5 (solute carrier family 17 (anion/sugar transporter), member 5) [NCBI Gene 235504] {aka 4631416G20Rik, 4732491M05, AST, ISSD, NSD, SD}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Myd88 (myeloid differentiation primary response gene 88) [NCBI Gene 17874], Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, Blnk (B cell linker) [NCBI Gene 17060] {aka BASH, Bca, Ly-57, Ly57, Lyw-57, SLP-65}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Lef1 (lymphoid enhancer binding factor 1) [NCBI Gene 16842] {aka 3000002B05, Lef-1}
- **Diseases:** inflammation (MESH:D007249), vasculitis (MESH:D014657), skin illnesses (MESH:D012871), AGA (MESH:D000505), cutaneous abscesses (MESH:D000038), ABF (MESH:D004761), atrophy (MESH:D001284), liver toxicity (MESH:D056486)
- **Chemicals:** sodium hydroxide (MESH:D012972), xylene (MESH:D014992), TRIzol (MESH:C411644), DHT (MESH:D013196), water (MESH:D014867), ceftazidime (MESH:D002442), hematoxylin (MESH:D006416), 2,4-dinitrophenylhydrazine (MESH:C004787), hydrochloric acid (MESH:D006851), eosin (MESH:D004801), porphyrin (MESH:D011166), ammonia (MESH:D000641), SDS (MESH:D012967), glutamine (MESH:D005973), ethanol (MESH:D000431), H&amp;E (MESH:D006371), sodium pentobarbital (MESH:D010424), agarose (MESH:D012685), paraffin (MESH:D010232), B8181 (-), ciprofloxacin (MESH:D002939), ceramides (MESH:D002518), glycopeptide (MESH:D006020), streptomycin sulfate (MESH:D013307), PVDF (MESH:C024865)
- **Species:** Bacteroides (genus) [taxon 816], Spirochaetota (phylum) [taxon 203691], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Cutibacterium acnes (species) [taxon 1747], Lactobacillus (genus) [taxon 1578], Staphylococcus epidermidis (species) [taxon 1282], Chryseobacterium (genus) [taxon 59732], Homo sapiens (human, species) [taxon 9606], Aeromonas (genus) [taxon 642], Streptococcus (genus) [taxon 1301], Acidobacteriota (phylum) [taxon 57723], Enterococcus (genus) [taxon 1350], Helicobacter (genus) [taxon 209], Aspergillus (genus) [taxon 5052], Aerococcus (genus) [taxon 1375], Bacteroidota (Bacteroides-Cytophaga-Flexibacter group, phylum) [taxon 976], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Cyanobacteriota (blue-green algae, phylum) [taxon 1117], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Proteus (genus) [taxon 210425], Acinetobacter (genus) [taxon 469], Mus musculus (house mouse, species) [taxon 10090], Achromobacter (genus) [taxon 222], Actinomycetota (actinobacteria, phylum) [taxon 201174], Deinococcota (phylum) [taxon 1297], Bacteroidia (class) [taxon 200643]
- **Mutations:** P0018M, P0013K, P0398L, C0105S

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13000086/full.md

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Source: https://tomesphere.com/paper/PMC13000086