NATURALLY OCCURING PLURIPOTENT
STEM CELLS WITHIN VIVO REGENERATIVE
FUNCTION— DISCOVERED BY PROFESSOR
DEZAWA, mD, PhD.

The Only Licensed Source of Real Dezawa MuseCells®

what are muse
cells™

Multilineage-differentiating Stress-Enduring (Muse) Cells™ are a distinct population of adult-derived stem cells discovered by Professor Mari Dezawa.

Unlike conventional MSCs, which act primarily through paracrine signaling, Muse Cells™ are naturally pluripotent, stress-resilient, and capable of spontaneous in vivo differentiation into all three germ layers—without genetic reprogramming or chemical induction.

This enables direct regeneration of functional tissue across multiple organ systems, with an exceptionally low risk of tumorigenicity.

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Meet the science team

Discovery of DEZAWA
MUSE Cells®

In 2010, Professor Mari Dezawa and her team at Tohoku University identified a rare, stress-resilient subpopulation of adult stem cells—now known as Dezawa MuseCells®.

What makes them different?

Spontaneous trilineage differentiation
Dezawa MuseCells® generate ectoderm, mesoderm, and endoderm lineages in vivo—without reprogramming or induction, and without teratoma formation.

Survival under extreme stress
They remain viable where most cells fail, including serum deprivation and oxidative stress (ROS exposure).

Embryonic marker expression without instability Dezawa MuseCells® express SSEA-3, a marker associated with embryonic stem cells, yet maintain a stable karyotype and low telomerase activity—even under stress.

With over 85 peer-reviewed studies and 120+ publications—including Phase II trials in Japan—Dezawa MuseCells® are supported by one of the most substantial evidence bases in regenerative medicine. Licensing offers partners exclusive access to this rigorously defined and validated platform.

Defined, patented, and validated in more than a decade of peer-reviewed research—Dezawa MuseCells® represent a trusted platform in regenerative medicine.

What Studies Show About Dezawa MuseCells®

TRAIT

DESCRIPTION

PLURIPOTENCY
Dezawa MuseCells® spontaneously differentiate into ectoderm, mesoderm, and endoderm lineages in vivo.
NON-TUMORIGENIC
Dezawa MuseCells® do not form teratoma—even in long-term immunodeficient mouse models.
STRESS-ENDURING
They survive harsh environments (hypoxia, serum deprivation) that other stem cells cannot.
IMMUNE TOLERANCE
HLA-G+, IDO+, HLA-DR- profile enables allogenic use without immunosuppressants
STABLE KARYOTYPE
Dezawa MuseCells® maintain chromosomal integrity and low telomerase, minimizing mutation risk.

Backed by 85+ peer-reviewed studies and 120+ publications, Dezawa MuseCells® offer one of the strongest evidence bases in the field of regenerative medicine.

All published information utilizes Dezawa MuseCells® that are manufactured in accordance with MCIs patented processes.

Research results apply only to Dezawa MuseCells® manufactured under Muse Cell Innovations®’ patented methods.

Claims are based on published studies of Dezawa MuseCells® made under Muse Cell Innovations®–licensed methods; results cannot be assumed for products manufactured differently.

Dezawa MuseCells® are the first and only MSC therapy that convinces clinicians and scientists alike because of its safety and efficacy. What the field has been waiting for more than 30 years, finally a stem cell treatment that works.

More than an MSC: Dezawa MuseCells® are a unique class of adult stem cells.

Feature

DEZAWA MuseCells®

Umbilical MSCs

POTENCY

Pluripotent (3 germ layers)
Multipotent (osteo, chondro, adipose)

HOMING

S1P–S1PR2 → injury site
Mostly trapped in lungs after IV

DIFFERENTIATION

Spontaneous in vivo
Requires chemical inducers

IMMUNE PRIVILEGE

HLA-G+, IDO+, HLA-DR-
Higher rejection risk

TUMOR RISK

None (low telomerase)
None (low telomerase)

PURITY

SSEA-3+ defined population
Heterogeneous adherent cell mix

Definitions & Regulator citations

This section provides clinical definitions, regulatory context, and essential distinctions for partners, reviewers, and regulators.

Dezawa MuseCells® detect S1P—a lipid released by injured tissue—and migrate directly via S1PR2 receptors. This active targeting distinguishes them from MSCs, which become passively trapped (e.g., in the lungs).

HLA-G⁺ inhibits NK and cytotoxic T-cell activation, enabling allogeneic (donor-based) use without immunosuppression.

SSEA-3 is a surface marker of pluripotent capability. Enriching for SSEA-3⁺ ensures the product is consistent, traceable, and therapeutically relevant.

This gene profile supports pluripotency without tumor risk. Let-7 suppresses oncogenic pathways; Lin28 is downregulated, reducing malignancy potential.

Dezawa MuseCells® show low telomerase, reducing risk of uncontrolled proliferation compared to iPSCs or ESCs.

Dezawa MuseCells® exhibit a stable chromosomal profile, even in long-term cultures—a key safety requirement for clinical-grade cell banking.

Unlike MSCs, Dezawa MuseCells® engulf apoptotic cells at the injury site—triggering spontaneous in vivo differentiation into functional tissue.

References available for download or regulator review.

Claims are based on published studies of Dezawa MuseCells® made under Muse Cell Innovations®–licensed methods; results cannot be assumed for products manufactured differently.

Explore Dezawa Muse Cells® Further:

See how they migrate, repair, and restore function in real models.

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