Mural cell

Mural cells are the vascular smooth muscle cells (vSMCs), and pericytes, of the microcirculation. Both types are in close contact with the endothelial cells lining the capillaries, and are important for vascular development and stability. Mural cells are involved in the formation of normal vasculature and are responsive to factors including platelet-derived growth factor B (PDGFB) and vascular endothelial growth factor (VEGF).[1][2] The weakness and disorganization of tumor vasculature is partly due to the inability of tumors to recruit properly organized mural cells.[3]

Cell type controversy

Mural cells were described for the first time in the late 19th century as contractile cells lining up around the endothelium. In reality, it was a variety of cells that had been observed and bundled up under the common name of Rouget cells. Later studies brought controversy about their contractility, and this remains an elusive point today.[4]

Pericytes, vSMCs, and many other perivascular cell types express very similar markers such as Platelet Derived Growth Factor Receptor Beta (PDGFR-B), aminopeptidase-N (CD13), chondroitin sulfate proteoglycan 4 (Ng2), or desmin, which makes their identification difficult and requires a combination of markers: for example vSMCs but not pericytes express alpha-smooth muscle actin (ACTA2). Nowadays, distinctively characterizing these cells requires a combination of markers, cellular location and morphology.

Lineage and zonation of mural cells

Typically, vSMCs wrap around larger vessels: they form a dense continuum spindling around arteries, arterioles and precapillary arterioles; while around postcapillary venules, vSMCs adopt a different morphology: individual cell bodies extending thing branching processes, that become more stellate-like around venules and veins.

The cell body of pericytes has a round shape extending a few processes in a longitudinal fashion along the capillaries.

Recently, efforts have been undertaken using single cell sequencing on mural cells to try to characterize their molecular signature along the blood vessels.[5] This showed that there is a zonation in their expression patterns by which they can be grouped into different subsets, but no singular markers have been found so far that can identify unequivocally any of the cell types.

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See also

References
  1. Fujimoto, Akihisa, Onodera, Hisashi, Mori, Akira, Isobe, Naoki, Yasuda, Seiichi, Oe, Hideaki, Yonenaga, Yoshikuni, Tachibana, Tsuyoshi & Imamura, Masayuki (2004) Vascular endothelial growth factor reduces mural cell coverage of endothelial cells and induces sprouting rather than luminal division in an HT1080 tumour angiogenesis model. International Journal of Experimental Pathology 85 (6), 355-364.
  2. Levéen, P.; Pekny, M.; Gebre-Medhin, S.; Swolin, B.; Larsson, E.; Betsholtz, C. (1994-08-15). "Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities". Genes & Development. 8 (16): 1875–1887. doi:10.1101/gad.8.16.1875. ISSN 0890-9369. PMID 7958863.
  3. Abramsson A, Berlin O, Papayan H, Paulin D, Shani M, Betsholtz C. (2002). Analysis of Mural Cell Recruitment to Tumor Vessels. Circulation 105:112.
  4. Armulik, Annika; Genové, Guillem; Betsholtz, Christer (August 2011). "Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises". Developmental Cell. 21 (2): 193–215. doi:10.1016/j.devcel.2011.07.001. ISSN 1534-5807. PMID 21839917.
  5. Vanlandewijck, Michael; He, Liqun; Mäe, Maarja Andaloussi; Andrae, Johanna; Ando, Koji; Del Gaudio, Francesca; Nahar, Khayrun; Lebouvier, Thibaud; Laviña, Bàrbara (2018-02-14). "A molecular atlas of cell types and zonation in the brain vasculature". Nature. 554 (7693): 475–480. doi:10.1038/nature25739. hdl:10138/301079. ISSN 0028-0836. PMID 29443965.


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