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Dingding An, Ph.D.

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Research Overview
Recognition of the important roles human microbiota plays in health and disease has forcefully blurred the distinction between self and non-self. Remarkably, in the human body, about 90% of cells and 99% of genes are of microbial origin. These microbes occupy every inch of the surface inside and outside us, as well as act as the boundary between our body and the environment. The association between humans and microbes has adapted to eons of co-evolution. Intricate interactions have evolved to seamlessly integrate into our eukaryotic biological networks and ultimately become absolutely indispensable with functions such as polysaccharide digestion, vitamin synthesis, immune system maturation and disease resistance. A wide range of disorders, including autoimmune diseases, metabolic syndromes, infectious diseases, and cancers are found to be results of abnormal host-microbe relationships. My research goal is to analyze the complex interactions between host and the microbiota and to illuminate new ways of promoting human health. The approach to achieve this goal is to dissect the host-microbe systems into specific temporal and spatial compartments and focus on key events in this relationship. We ask questions not only about “what” and “how” but also about “when” and “where.” In line with these priorities, we study 1) how early microbial exposure modulates host development and 2) how mucosa-associated microbes direct host homeostasis.

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Zhang H, Guan M, Townsend KL, Huang TL, An D, Yan X, Xue R, Schulz TJ, Winnay J, Mori M, Hirshman MF, Kristiansen K, Tsang JS, White AP, Cypess AM, Goodyear LJ, Tseng YH. MicroRNA-455 regulates brown adipogenesis via a novel HIF1an-AMPK-PGC1a signaling network. EMBO Rep. 2015 Oct; 16(10):1378-93. PMID: 26303948.
    Citations: 21     Fields:    Translation:HumansAnimalsCells
  2. Wang H, Ma H, Zheng W, An D, Na C. Multifunctional and recollectable carbon nanotube ponytails for water purification. ACS Appl Mater Interfaces. 2014 Jun 25; 6(12):9426-34. PMID: 24806877.
    Citations:    Fields:    Translation:HumansCellsPHPublic Health
  3. An D, Oh SF, Olszak T, Neves JF, Avci FY, Erturk-Hasdemir D, Lu X, Zeissig S, Blumberg RS, Kasper DL. Sphingolipids from a symbiotic microbe regulate homeostasis of host intestinal natural killer T cells. Cell. 2014 Jan 16; 156(1-2):123-33. PMID: 24439373.
    Citations: 103     Fields:    Translation:AnimalsCells
  4. An D, Kasper DL. Testosterone: more than having the guts to win the Tour de France. Immunity. 2013 Aug 22; 39(2):208-10. PMID: 23973219.
    Citations:    Fields:    Translation:Animals
  5. Olszak, T.*, An, D.*, Zeissig, S., Vera, M.P., Richter, J., Franke, A., Glickman, J. N., Siebert, R., Baron, R. M., Kasper, D. L., Blumberg, R. S. (* equal-contribution first author). Microbial exposure during early life has persistent effects on natural killer T cell function. Science. 2012; 336(6080):489-93.
  6. An D, Na C, Bielawski J, Hannun YA, Kasper DL. Membrane sphingolipids as essential molecular signals for Bacteroides survival in the intestine. Proc Natl Acad Sci U S A. 2011 Mar 15; 108 Suppl 1:4666-71. PMID: 20855611.
    Citations: 30     Fields:    Translation:HumansCells
  7. Siehnel, R., Traxler, B., An, D., Parsek, M. R., Schaefer, A. L., Singh, P.K. . A unique regulator controls the activation threshold of quorum-regulated genes in Pseudomonas aeruginosa. Proc. Natl. Acad. Sci .USA. 2010 Apr 27;107(17):7916-21. 2010; 17(107):7916-21.
  8. An D, Apidianakis Y, Boechat AL, Baldini RL, Goumnerov BC, Rahme LG. The pathogenic properties of a novel and conserved gene product, KerV, in proteobacteria. PLoS One. 2009 Sep 25; 4(9):e7167. PMID: 19779606.
    Citations: 4     Fields:    Translation:HumansAnimalsCells
  9. An D, Parsek MR. The promise and peril of transcriptional profiling in biofilm communities. Curr Opin Microbiol. 2007 Jun; 10(3):292-6. PMID: 17573234.
    Citations: 31     Fields:    Translation:Cells
  10. An D, Danhorn T, Fuqua C, Parsek MR. Quorum sensing and motility mediate interactions between Pseudomonas aeruginosa and Agrobacterium tumefaciens in biofilm cocultures. Proc Natl Acad Sci U S A. 2006 Mar 07; 103(10):3828-33. PMID: 16537456.
    Citations: 41     Fields:    Translation:Cells
  11. Landry RM, An D, Hupp JT, Singh PK, Parsek MR. Mucin-Pseudomonas aeruginosa interactions promote biofilm formation and antibiotic resistance. Mol Microbiol. 2006 Jan; 59(1):142-51. PMID: 16359324.
    Citations: 32     Fields:    Translation:HumansCells
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Funded by the NIH/NCATS Clinical and Translational Science Award (CTSA) program, grant number UL1TR001102, and through institutional support from Harvard University, Harvard Medical School, Harvard T.H. Chan School of Public Health, Beth Israel Deaconess Medical Center, Boston Children's Hospital, Brigham and Women's Hospital, Massachusetts General Hospital and the Dana Farber Cancer Institute.