Mark Horowitz, PhD

Professor of Orthopaedics and Rehabilitation; Vice Chair for Research

Research Departments & Organizations

Orthopaedics & Rehabilitation

Diabetes Research Center

Fellowship Training

Obesity Research Working Group

Rheumatic Diseases Research Core

Office of Cooperative Research

Research Interests

Adipocytes; Bone and Bones; Bone Remodeling; Mesenchymal Stem Cell Transplantation; Orthopedics; Osteoblasts; Osteoclasts

Research Summary

Interactions between the skeletal, immune, and hematopoietic systems as they relate to normal and pathologic bone remodeling. Transgenic mice are used to investigate osteoblast and osteoclast development.

Specialized Terms: Osteoimmunology; Osteoblasts; Osteoclasts; Adipocytes; Bone remodeling; Mesenchymal stem cell differentiation; B cell transcription factors and bone

Extensive Research Description

The laboratory is focused on two areas. The first, is osteoimmunology and the second is the relationship of adipose tissue to bone. To this end we are examining a number of transgenic animal models many of which have specific transcription factors deleted, one result being bone alterations. As an example the loss of GATA-1, a transcription factor required for megakaryocyte differentiation, have a phenotype characterized by an increase in the number of megakaryocytes, no functional platelets and a massive increase in both trabecular and cortical bone. We are in the process of characterizing both the bone phenotype and the underlying mechanism responsible for the increased bone mass. In addition, we are looking at mice deficient in transcription factors required for B cell differentiation. Ebf1 deficient mice lack B cells but also have increased bone formation and increased marrow fat. Increased fat usually occurs at the expense of osteoblastogenesis. Because of the lipodystrophic phenotype of Ebf1 deficient mice, we are developing models for increased marrow fat. Marrow fat increases with age. However, is function as well as its origin are unknown. In a separate project, we are isolating cells from inside, rather than on bone surfaces. These cells are heterogeneous and have some characteristics of osteocytes.

  • Analysis of the bone and fat phenotype of mice lacking the B cell transcription factors Ebf1 and Pax5
  • Analysis of the bone phenotype of mice lacking GATA1
  • Isolation and characterization of bone cells from inside bone (osteocytes).
  • Develop mouse models for marrow fat.

Selected Publications

See list of PubMed publications

Edit this profile

Contact Info

Mark Horowitz, PhD
Mailing Address
Orthopaedics & RehabilitationP.O. Box 208071
New Haven, CT 06520-8071