LMCD1 is a member of the LIM protein family, characterized by an N-terminal cysteine-rich region, two C-terminal LIM domains, and a central PET domain . It functions as a transcriptional cofactor, interacting with factors like GATA6 and NFATc1 to regulate gene expression in cardiac, lung, and vascular tissues . LMCD1 antibodies enable detection and functional analysis of this protein in research settings, including Western blot (WB), immunohistochemistry (IHC), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA) .
LMCD1 antibodies have elucidated species-specific regulatory mechanisms in vascular smooth muscle cells (VSMCs):
Human VSMCs: LMCD1 acts as an activator of E2F1 and NFATc1, promoting CDC6 (cell cycle progression) and IL-33 (pro-inflammatory cytokine) expression, driving proliferation and migration .
Mouse VSMCs: LMCD1 functions as a repressor of E2F1/NFATc1, with thrombin-induced myristoylation abolishing repression .
Clinical Relevance: Increased LMCD1 expression correlates with human stenotic arteries, while reduced levels are observed in mouse neointimal lesions .
LMCD1 antibodies identified LMCD1 as a profibrotic factor in scleroderma-associated interstitial lung disease (SSc-ILD):
Mechanisms: LMCD1 depletion reduces TGFβ-induced collagen I, fibronectin, and SMA expression in fibroblasts .
Localization: LMCD1 co-localizes with SMA in fibrotic lung tissue, indicating a role in myofibroblast activation .
In human bone marrow stromal cells (BMSCs), LMCD1 knockdown inhibits osteogenic markers (e.g., COL1A1, RUNX2), while overexpression enhances mineralization .
Sample Preparation: Lyse cells in RIPA buffer, resolve proteins via SDS-PAGE.
Transfer: Transfer to PVDF membrane, block with 5% BSA.
Detection: Incubate with 1:1,000 diluted antibody, followed by HRP-conjugated secondary antibody .