β2 microglobulin promotes pericyte proliferation through toll-like receptor 4

Pericytes are perivascular cells that contribute to maintaining vascular integrity and central nervous system homeostasis. β<sub>2</sub>-microglobulin (B2M) is a component of the major histocompatibility complex class I molecule; it has recently been implicated in age-related and injury-associated inflammation. Here, we investigated the phenotypic and transcriptomic effects of B2M on mouse brain pericytes in vitro. B2M treatment increased Bromodeoxyuridine (BrdU) incorporation into the cultured pericytes as well as the number of Ki67-positive pericytes. Morphologically, B2M promoted pericyte extension. Toll-like receptor 4 (TLR4), one of the key molecules that regulates B2M function, was involved in the B2M-dependent pericyte proliferation. These findings were consistent with RNA-seq results showing differential expression of genes related to cell proliferation. These results suggest that B2M directly acts on pericytes and regulates part of their functional responses through TLR4 signaling.

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Publication Details

Journal
Journal of Pharmacological Sciences
Published
2025-12-04
DOI
https://doi.org/10.1016/j.jphs.2025.12.001
Citations
1
Primary Topic
Barrier Structure and Function Studies
Type
article
Field-Weighted Citation Impact
0.84
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article

β2 microglobulin promotes pericyte proliferation through toll-like receptor 4

Yoshino Yonezu, Hidemi Misawa, Akiko Uyeda, Rieko Muramatsu
1 citations
Journal of Pharmacological Sciences
Barrier Structure and Function Studies
0.84
article

β2 microglobulin promotes pericyte proliferation through toll-like receptor 4

Yoshino Yonezu, Hidemi Misawa, Akiko Uyeda, Rieko Muramatsu
article en
1 citations

Abstract

Pericytes are perivascular cells that contribute to maintaining vascular integrity and central nervous system homeostasis. β<sub>2</sub>-microglobulin (B2M) is a component of the major histocompatibility complex class I molecule; it has recently been implicated in age-related and injury-associated inflammation. Here, we investigated the phenotypic and transcriptomic effects of B2M on mouse brain pericytes in vitro. B2M treatment increased Bromodeoxyuridine (BrdU) incorporation into the cultured pericytes as well as the number of Ki67-positive pericytes. Morphologically, B2M promoted pericyte extension. Toll-like receptor 4 (TLR4), one of the key molecules that regulates B2M function, was involved in the B2M-dependent pericyte proliferation. These findings were consistent with RNA-seq results showing differential expression of genes related to cell proliferation. These results suggest that B2M directly acts on pericytes and regulates part of their functional responses through TLR4 signaling.

Journal of Pharmacological SciencesVol. 160(1)
Keio University (JP), National Center of Neurology and Psychiatry (JP)
Openalex Percentile: Top 19%
Barrier Structure and Function Studies
0.84
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