Target intelligence / Profile preview

Bone marrow mesenchymal stem cell (BM-MSC)

Target
BM-MSC
Molecular classification
Other, Multipotent adult stem cell, Stromal cell
01

Overview

Bone marrow mesenchymal stem cell (BM-MSC) refers to a population of non-hematopoietic, multipotent, plastic-adherent adult stem cells principally resident in the bone marrow but also identifiable in other tissues[1][2][4]. BM-MSCs are characterized by their ability to self-renew and to differentiate into multiple mesenchymal lineages, such as bone (osteoblasts), fat (adipocytes), cartilage (chondrocytes), and, under certain conditions, muscle and other cell types[1][3][5]. In addition to their differentiation potential, BM-MSCs secrete a variety of bioactive molecules, thereby modulating tissue repair, immune responses, and inflammation primarily through paracrine mechanisms rather than by direct replacement of damaged cells[3][4][6]. They form a significant component of the hematopoietic niche in the marrow, supporting hematopoietic stem cells, and are under clinical investigation for use in regenerative medicine and immunomodulatory therapies[2][6]. There are challenges in their use, including heterogeneity of populations, risk of senescence, and the theoretical risk of malignant transformation upon extensive culture[2]. Note: BM-MSCs, as a cell population, are not a therapeutic target in the sense of a molecular drug target (receptor, enzyme, transporter). Rather, they are a source of cellular therapeutics, acting as living drugs in cell therapy. Thus, "Bone marrow mesenchymal stem cell" is not a canonical molecule or receptor target; it is a heterogeneous cell population[2][3][5]. Because of this, the entry is marked as is_incorrect: true for a molecule/receptor target list.

Other names
Mesenchymal stromal cell (bone marrow)MSC (bone marrow)Bone marrow MSCBM stromal cell
02

Biological functions

Differentiation into osteoblasts, chondrocytes, adipocytes, myocytesSupport of hematopoiesisTissue repair and regenerationImmunomodulationSecretion of bioactive molecules (paracrine signaling)
03

Disease associations

Cancer (e.g., potential for malignant transformation)InflammationCardiovascular diseaseImmune disordersGraft-vs-host diseaseTissue regeneration/degenerationOther
04

Safety considerations

Heterogeneity and poorly defined cell populationsSenescence in cultureRisk of malignant transformation (sarcoma)Immunogenicity after prolonged cultureUnknown long-term effects in clinical applications[2]
05

Biomarkers

CD73CD90CD105Lack of CD34, CD14, CD45Plastic adherence in cultureOther surface/cytoplasmic markers: OCT4, SOX11, NGFR, LEPR, SSEA-3, etc.[1][3][4]

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