Pax7 Is Required for the Specification of Myogenic Satellite Cells

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Pax7 Is Required for the Specification of Myogenic Satellite Cells Patrick Seale, Luc A Sabourin, Adele Girgis-Gabardo, Ahmed Mansouri, Peter Gruss, Michael A Rudnicki  Cell  Volume 102, Issue 6, Pages 777-786 (September 2000) DOI: 10.1016/S0092-8674(00)00066-0

Figure 1 Pax7 Is Expressed Specifically in Proliferating Myoblasts (A) Pax7 was expressed at high levels in proliferating wild-type myoblasts (Wt-Mb) and MyoD-deficient cells (MyoD−/− Mb) cells and downregulated in response to differentiation conditions (Wt-D and MyoD−/− D). (B) Expression of Pax7 was specific to myogenic cells, with low levels detected in C2C12 myoblasts. (C) Pax7 was not detected in RNA from a panel of tissues. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 2 Expression of Pax7 in Muscle Satellite Cells (A) In situ hybridization revealed that Pax7 mRNA was expressed at a frequency and location consistent with specific expression in satellite cells and myogenic precursor cells. (B) Pax7 expression was associated with PI-positive nuclei (40× magnification). (C and D) High magnification (200×) of Pax7-expressing cell in wild-type muscle was characteristic of a satellite cell residing beneath the basal lamina. (E and F) Increased numbers of cells expressed Pax7 in regenerating mdx muscle (40×). Black and white arrowheads indicate cells stained positive for Pax7 mRNA and PI-positive nuclei, respectively. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 3 Skeletal Muscle Deficiency in Pax7−/− Mice (A) Seven-day-old Pax7 mutant animals were approximately one-half the weight of wild-type animals and had splayed hind limbs and an abnormal gait. (B and C) HE-stained tibialis anterior muscle sections (40×) revealed a normal histological appearance of Pax7 mutant muscle (C), but fiber diameter was reduced 1.5-fold compared with that of wild-type muscle (B). (D and E) The diaphragm of a mutant animal (E) shown here in cross-section was significantly thinner than that in wild-type animals (D) (40×). Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 4 Absence of Myoblasts in Cultures Derived from Pax7−/− Muscle Primary cell cultures were analyzed by phase microscopy (A and F) and by immunocytochemistry with anti-desmin (B and G) and anti-c-Met (D and I) antibodies. Cells stained with antibodies were counterstained with Hoechst 33342 (C, E, H, and J) to show all nuclei. Black arrowheads indicate satellite cell-derived myoblasts; white arrowheads indicate immunoreactive cells and corresponding nuclei. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 5 Complete Ablation of Satellite Cells in Pax7−/− Muscle Transmission electron micrographs of 7- to 10-day-old Pax7+/+ (A through D) and Pax7−/− (E and F) muscle. (A and C) Satellite cells (SC) are readily identified in Pax7+/+ muscle (7500×). (B and D) High magnification of satellite cells clearly revealed the plasma membrane (black arrowheads) separating the satellite cell from its adjacent myofiber, the continuous basal lamina surrounding the satellite cell and myofiber, and the heterochromatic appearance of the nucleus (20,000×). (E and F) Myonuclei (fiber nuclei) (MN) but not satellite cells were present in Pax7 mutant muscles. Other ultrastructural differences were not detected. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 6 Enhanced Hematopoietic Potential of Pax7−/− Muscle–Derived Pluripotent Stem Cells (A through D) FACS analysis of Hoechst-stained muscle-derived cells demonstrated approximately equal numbers of verapamil-sensitive SP cells in both Pax7+/+ (A and B) and Pax7−/− (C and D) muscles. (E) MHC-positive muscle colonies predominate in stem-cell medium/methylcellulose cultures of Pax7+/+ muscle cells. (F through H) Pax7−/− muscle cells have increased hematopoietic potential (F) and generate granulocyte and monocyte colonies verified by Ly-6G immunoreactivity (G and H). (I) Colony-forming assay of muscle cells cultured in stem-cell medium/methylcellulose over a period of 2 weeks demonstrated almost a 10-fold increase in hematopoietic potential of Pax7 mutant stem cells. Other cells represent both fibroblasts and adipocytes. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)

Figure 7 Role for Pax7 in the Specification of Satellite Cells Muscle-derived pluripotent stem cells primarily give rise to myoblasts when cultured in stem-cell medium. By contrast, Pax7−/− muscle stem cells exhibit almost a 10-fold increase in propensity toward hematopoietic differentiation and are incapable of forming adult myoblasts. These data therefore implicate Pax7 in regulating the specification of adult muscle satellite cells by restricting the fate of pluripotent stem cells. Taken together, these experiments suggest the following hypothesis. Pluripotent stem cells (MSC) within muscle represent the progenitors of sublaminar satellite cells that are specified following induction of Pax7. Satellite cells are subsequently activated in response to physiological stimuli to generate daughter myogenic precursor cells (MPC) before terminal differentiation into new or previously existing fibers. Cell 2000 102, 777-786DOI: (10.1016/S0092-8674(00)00066-0)