| Name | long intergenic non-protein coding RNA 554 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough none of the studies provided address LINC00554 directly, they collectively delineate the multifaceted roles of semaphorin 4D (Sema4D, also known as CD100) and its receptors as master regulators of diverse cellular processes. In the nervous system, Sema4D contributes to axonal guidance, modulates neurite outgrowth, and influences oligodendrocyte survival and differentiation—functions that are essential for proper neural circuit formation as well as for regenerative responses following injury."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its neural functions, Sema4D exerts potent effects in nonneuronal tissues. It acts as a critical mediator in the immune system by promoting T-cell activation, fine-tuning B-cell receptor signaling, and enhancing dendritic cell and macrophage responsiveness. In parallel, Sema4D modulates angiogenesis and vascular remodeling, influences platelet aggregation and thrombus formation, and even governs bone remodeling by affecting osteoclast and osteoblast activity. These studies highlight its ability to trigger proteolytic shedding and to signal via receptors such as plexin‑B1 and CD72, thereby orchestrating processes ranging from inflammatory responses to tissue repair."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "16"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, additional investigations extend the impact of Sema4D signaling to the regulation of microglial activation, synapse development, and tissue‐specific remodeling events such as retinal phagocytosis, estrogen‐dependent epithelial apoptosis, and the control of osteoblast–osteoclast communication. Sema4D thereby emerges as a pivotal factor that, through mechanisms including proteolytic cleavage and receptor complex formation, modulates cell migration, proliferation, and programmed cell death in contexts as varied as neuroinflammation, tumor progression, and vascular as well as bone homeostasis. In the absence of any evidence about LINC00554 in these reports, the intricate regulatory circuitry governed by Sema4D may nonetheless serve as a conceptual framework for future studies exploring whether noncoding RNAs such as LINC00554 modulate similar signaling networks."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "17", "end_ref": "32"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Atsushi Kumanogoh, Kazuhiro Suzuki, EweSeng Ch'ng, et al. 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| Synonyms | lncZic2 |
| NCBI Gene ID | 100861542 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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LINC00554 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for LINC00554 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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