Andrew lassar
Andrew B. Lassar, Ph.D.
Professor of Biological Chemistry and Molecular Pharmacology

Current work in the Lassar Lab focuses on the transcriptional regulatory pathways that regulate chondrocyte formation and maturation, elucidation of how mechanical loading regulates gene expression in the joint, a molecular dissection of the signals and transcription factors that maintain articular cartilage stem cells, and the development of a gene therapy model to treat osteoarthritis.

 

Andrew Lassar received his B. A. from Yale (’75) and his Ph.D. (’83) from Washington University in St. Louis, where he worked with Bob Roeder. He then performed his postdoctoral work in the laboratory of Hal Weintraub at the Fred Hutchinson Cancer Research Center in Seattle, WA.  In 1991, he established his own lab in the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School, where he runs a research lab and teaches developmental biology.

 

Research:

The overarching goal of the Lassar lab is to understand how different cells types (i.e., articular or epiphyseal chondrocytes, ligaments and synoviocytes) emerge from a common precursor population during the formation of the synovial joint. Towards this goal, work in the Lassar lab focuses on the transcriptional regulatory pathways that regulate chondrocyte formation and maturation, elucidation of how mechanical loading regulates gene expression in the joint, and a molecular dissection of the signals and transcription factors that maintain articular cartilage stem cells. We are studying how the initial cartilage template is induced in the embryo and are trying to elucidate how chondrocytes “decide” whether to undergo maturation, which leads to endochondral ossification, or remain immature, as in the articular cartilage of our joints. The Lassar lab has recently identified a stem cell population for articular cartilage; and we are employing genome-wide ATAC-Seq, ChIP-Seq, and RNA-Seq methodologies to elucidate the transcriptional regulators that control both the induction and maintenance of these stem cells.

 

Identification of factors that are necessary for Sox9 to activate the chondrogenic differentiation program.The transcription factor Sox9 is critical for mesenchymal cells to commit to and execute the chondrogenic differentiation program; in its absence chondrogenesis is blocked. Sox9 both directly activates chondrocyte differentiation markers and induces the expression of Sox5 and Sox6, which work together with Sox9 to activate the chondrocyte differentiation program. However, in addition to its essential role in initiating the chondrogenic differentiation program, Sox9 is also expressed in a number of other cells types, including neural stem cells, oligodendrocyte precursors, intestinal stem cells, hair follicle stem cells, and the developing testis. Taken together, these findings indicate that the ability of Sox9 to induce the chondrocyte differentiation program is context dependent, suggesting that additional factors are necessary for Sox9 to activate chondrocyte-specific transcriptional targets. We have recently identified additional chondrogenic competence factors, and are studying how these factors establish the competence for Sox9 to induce chondrocyte formation.

 

Identification of the transcriptional network that controls the formation and maintenance of articular cartilage stem cells. Lineage tracing studies have suggested that growth plate and articular chondrocytes arise from distinct progenitor populations, such that articular chondrocytes share a common origin with synovial cells that line the joint cavity. The superficial-most layer of articular cartilage is distinguished from deeper layers by expression of lubricin. Lubricin is a secreted proteoglycan encoded by the Prg4 locus, and is highly expressed by both superficial zone articular chondrocytes and synoviocytes, and notably is expressed in the progenitor cells of the articular cartilage. We have recently mapped the DNA sequences that control the expression of Prg4/lubricin by performing ATAC-Seq analysis (which detects regions of the genome with increased accessibility for in vitro transposon insertion). This approach identified four regions surrounding the Prg4 locus that display increased accessibility for in vitro transposon insertion specifically in lubricin-expressing superficial zone chondrocytes, and which work in combination to drive reporter gene expression specifically in superficial zone chondrocytes. A bioinformatics analysis of both this ATAC-Seq data and complementary RNA-Seq data has identified transcription factor families that are specifically expressed in the Prg4/lubricin-expressing stem cells of articular cartilage. We are currently determining the role of these transcription factors in regulating either the formation or maintenance of articular cartilage stem cells; with the goal of employing this knowledge to restore articular cartilage stem cells in degenerating joint tissue.

Address: 

Room C - 305A

240 Longwood Avenue

Boston, MA 02115

Publications View
PTHrP targets HDAC4 and HDAC5 to repress chondrocyte hypertrophy.
Authors: Authors: Nishimori S, Lai F, Shiraishi M, Kobayashi T, Kozhemyakina E, Yao TP, Lassar AB, Kronenberg HM.
JCI Insight
View full abstract on Pubmed
Finding MyoD and lessons learned along the way.
Authors: Authors: Lassar AB.
Semin Cell Dev Biol
View full abstract on Pubmed
Superficial cells are self-renewing chondrocyte progenitors, which form the articular cartilage in juvenile mice.
Authors: Authors: Li L, Newton PT, Bouderlique T, Sejnohova M, Zikmund T, Kozhemyakina E, Xie M, Krivanek J, Kaiser J, Qian H, Dyachuk V, Lassar AB, Warman ML, Barenius B, Adameyko I, Chagin AS.
FASEB J
View full abstract on Pubmed
Identification of a Prg4-expressing articular cartilage progenitor cell population in mice.
Authors: Authors: Kozhemyakina E, Zhang M, Ionescu A, Ayturk UM, Ono N, Kobayashi A, Kronenberg H, Warman ML, Lassar AB.
Arthritis Rheumatol
View full abstract on Pubmed
A pathway to bone: signaling molecules and transcription factors involved in chondrocyte development and maturation.
Authors: Authors: Kozhemyakina E, Lassar AB, Zelzer E.
Development
View full abstract on Pubmed
BMP-mediated induction of GATA4/5/6 blocks somitic responsiveness to SHH.
Authors: Authors: Daoud G, Kempf H, Kumar D, Kozhemyakina E, Holowacz T, Kim DW, Ionescu A, Lassar AB.
Development
View full abstract on Pubmed
Fibroblast growth factor maintains chondrogenic potential of limb bud mesenchymal cells by modulating DNMT3A recruitment.
Authors: Authors: Kumar D, Lassar AB.
Cell Rep
View full abstract on Pubmed
Mechanical motion promotes expression of Prg4 in articular cartilage via multiple CREB-dependent, fluid flow shear stress-induced signaling pathways.
Authors: Authors: Ogawa H, Kozhemyakina E, Hung HH, Grodzinsky AJ, Lassar AB.
Genes Dev
View full abstract on Pubmed
GATA6 is a crucial regulator of Shh in the limb bud.
Authors: Authors: Kozhemyakina E, Ionescu A, Lassar AB.
PLoS Genet
View full abstract on Pubmed
Evolutionary conservation of Nkx2.5 autoregulation in the second heart field.
Authors: Authors: Clark CD, Zhang B, Lee B, Evans SI, Lassar AB, Lee KH.
Dev Biol
View full abstract on Pubmed