Matthew R. Jones, PhD
Associate Professor
Boston University Chobanian & Avedisian School of Medicine
Medicine
Pulmonary, Allergy, Sleep & Critical Care Medicine

PhD, Boston University School of Medicine
BA, University of Delaware



I have expertise in innate immunology, pulmonary epithelial and lymphatic biology and post-transcriptional mechanisms of gene expression.

Diversity, Equity, Inclusion and Accessibility

Whether in the lab or in the classroom, I am fully committed to fostering and enhancing a training environment here at BUSM that prioritizes diversity, equity, inclusion and accessibility. Diverse groups have been shown to be more productive, more innovative and engage with greater levels of critical reasoning; all of which are critical for thriving biomedical research and educational programs. Towards this goal, I have served to increase diversity at all levels of trainees; from postbac, graduate and medical students to faculty recruitment. I have participated in the Postbaccalaureate Research Education Programs (PREP) by helping to prepare students for graduate school interviews. This program helps develop research experiences for students from under-represented groups that strive for a career in research or medicine. In my role in medical school admissions, we embrace a holistic review of applicants that acknowledges strength of character, distance traveled, grit and perseverance. For graduate school admissions and as Director of the Graduate Program in Molecular and Translational Medicine, I serve to enhance the recruitment of under-represented groups through creation of mechanisms such as the Emerging Scholar’s Award which is now supported by multiple Departments throughout the Medical School. The goal of this award is to mitigate expensive relocation to the Boston area. With my involvement with the TL1 Regenerative Medicine Training Program we have enhanced a strong track record of supporting the recruitment and enrollment of under-represented trainees. As participating faculty in the Pulmonary Center, I serve as a member of the DEIA faculty recruitment committee. In all aspects of my professional and personal life, I am firmly dedicated to diversity, equity, inclusion and accessibility efforts and I actively and reflectively endeavor to continuously improve upon them.

Member
Boston University
Pulmonary Center


Member
Boston University
Evans Center for Interdisciplinary Biomedical Research


Member
Boston University
Genome Science Institute


Graduate Faculty (Primary Mentor of Grad Students)
Boston University Chobanian & Avedisian School of Medicine, Graduate Medical Sciences




Biology of Lymphangiogenesis in the Adult Lung
07/01/2022 - 06/30/2026 (Multi-PI)
PI: Matthew R. Jones, PhD
NIH/National Heart, Lung, and Blood Institute
5R01HL164612-03

Origins and functional roles of Miwi2-positive multiciliated cells during inflammation
03/07/2018 - 02/28/2023 (Multi-PI)
PI: Matthew R. Jones, PhD
NIH/National Heart, Lung, and Blood Institute
5R01HL136725-04

MicroRNA Uridylation by Zcchc11 Regulates Pulmonary Inflammation
07/12/2010 - 05/31/2017 (PI)
NIH/National Heart, Lung, and Blood Institute
5R01HL104053-05

The piRNA binding protein Miwi2 promotes cytokine expression during bacterial pneumonia
09/01/2015 - 06/01/2016 (Key Person / Mentor)
PI: Gregory Wasserman, PhD
NIH/National Heart, Lung, and Blood Institute
1F31HL127978-01



Title


Yr Title Project-Sub Proj Pubs
2024 Biology of Lymphangiogenesis in the Adult Lung 5R01HL164612-03
2023 Biology of Lymphangiogenesis in the Adult Lung 5R01HL164612-02
2022 Biology of Lymphangiogenesis in the Adult Lung 1R01HL164612-01
2021 Origins and functional roles of Miwi2-positive multiciliated cells during inflammation 5R01HL136725-04 3
2020 Origins and functional roles of Miwi2-positive multiciliated cells during inflammation 5R01HL136725-03 3
2019 Origins and functional roles of Miwi2-positive multiciliated cells during inflammation 5R01HL136725-02 3
2018 Origins and functional roles of Miwi2-positive multiciliated cells during inflammation 1R01HL136725-01A1 3
2014 MicroRNA uridylation by Zcchc11 regulates pulmonary inflammation 5R01HL104053-05 18
2013 MicroRNA uridylation by Zcchc11 regulates pulmonary inflammation 5R01HL104053-04 18
2012 MicroRNA uridylation by Zcchc11 regulates pulmonary inflammation 5R01HL104053-03 18
Showing 10 of 12 results. Show All Results

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.

iCite Analysis       Copy PMIDs To Clipboard

  1. Etesami NS, Barker KA, Shenoy AT, De Ana CL, Arafa EI, Grifno GN, Matschulat AM, Vannini ME, Pihl RMF, Breen MP, Soucy AM, Goltry WN, Ha CT, Betsuyaku H, Browning JL, Varelas X, Traber KE, Jones MR, Quinton LJ, Maglione PJ, Nia HT, Belkina AC, Mizgerd JP. B cells in the pneumococcus-infected lung are heterogeneous and require CD4+ T cell help including CD40L to become resident memory B cells. Front Immunol. 2024; 15:1382638.View Related Profiles. PMID: 38715601; PMCID: PMC11074383; DOI: 10.3389/fimmu.2024.1382638;
     
  2. Crossey E, Carty S, Shao F, Henao-Vasquez J, Ysasi AB, Zeng M, Hinds A, Lo M, Tilston-Lunel A, Varelas X, Jones MR, Fine A. Influenza Induces Lung Lymphangiogenesis Independent of YAP/TAZ Activity in Lymphatic Endothelial Cells. Res Sq. 2024 Feb 27.View Related Profiles. PMID: 38463972; PMCID: PMC10925403; DOI: 10.21203/rs.3.rs-3951689/v1;
     
  3. Lyon De Ana C, Shenoy AT, Barker KA, Arafa EI, Etesami NS, Korkmaz FT, Soucy AM, Breen MP, Martin IMC, Tilton BR, Devarajan P, Crossland NA, Pihl RMF, Goltry WN, Belkina AC, Jones MR, Quinton LJ, Mizgerd JP. GL7 ligand expression defines a novel subset of CD4+ TRM cells in lungs recovered from pneumococcus. Mucosal Immunol. 2023 Oct; 16(5):699-710.View Related Profiles. PMID: 37604254; PMCID: PMC10591822; DOI: 10.1016/j.mucimm.2023.07.004;
     
  4. Jones MR, Lingampally A, Ahmadvand N, Chong L, Wu J, Wilhem J, Vazquez-Armendariz AI, Ansari M, Herold S, Ornitz DM, Schiller HB, Chao CM, Zhang JS, Carraro G, Bellusci S. FGFR2b signalling restricts lineage-flexible alveolar progenitors during mouse lung development and converges in mature alveolar type 2 cells. Cell Mol Life Sci. 2022 Nov 29; 79(12):609. PMID: 36445537; PMCID: PMC9708820; DOI: 10.1007/s00018-022-04626-2;
     
  5. Ahmadvand N, Lingampally A, Khosravi F, Vazquez-Armendariz AI, Rivetti S, Jones MR, Wilhelm J, Herold S, Barreto G, Koepke J, Samakovlis C, Carraro G, Zhang JS, Al Alam D, Bellusci S. Fgfr2b signaling is essential for the maintenance of the alveolar epithelial type 2 lineage during lung homeostasis in mice. Cell Mol Life Sci. 2022 May 19; 79(6):302. PMID: 35587837; PMCID: PMC9120111; DOI: 10.1007/s00018-022-04327-w;
     
  6. Arafa EI, Shenoy AT, Barker KA, Etesami NS, Martin IM, Lyon De Ana C, Na E, Odom CV, Goltry WN, Korkmaz FT, Wooten AK, Belkina AC, Guillon A, Forsberg EC, Jones MR, Quinton LJ, Mizgerd JP. Recruitment and training of alveolar macrophages after pneumococcal pneumonia. JCI Insight. 2022 Mar 08; 7(5).View Related Profiles. PMID: 35133985; PMCID: PMC8983128; DOI: 10.1172/jci.insight.150239;
     
  7. Na E, Allen E, Baird LA, Odom CV, Korkmaz FT, Shenoy AT, Matschulat AM, Jones MR, Kotton DN, Mizgerd JP, Varelas X, Traber KE, Quinton LJ. Epithelial LIF signaling limits apoptosis and lung injury during bacterial pneumonia. Am J Physiol Lung Cell Mol Physiol. 2022 Apr 01; 322(4):L550-L563.View Related Profiles. PMID: 35137631; PMCID: PMC8957336; DOI: 10.1152/ajplung.00325.2021;
     
  8. Sanders NL, Martin IMC, Sharma A, Jones MR, Quinton LJ, Bosmann M, Mizgerd JP. Neutrophil Extracellular Traps as an Exacerbating Factor in Bacterial Pneumonia. Infect Immun. 2022 03 17; 90(3):e0049121.View Related Profiles. PMID: 35130455; PMCID: PMC8929384; DOI: 10.1128/iai.00491-21;
     
  9. Shenoy AT, Lyon De Ana C, Arafa EI, Salwig I, Barker KA, Korkmaz FT, Ramanujan A, Etesami NS, Soucy AM, Martin IMC, Tilton BR, Hinds A, Goltry WN, Kathuria H, Braun T, Jones MR, Quinton LJ, Belkina AC, Mizgerd JP. Antigen presentation by lung epithelial cells directs CD4+ TRM cell function and regulates barrier immunity. Nat Commun. 2021 10 05; 12(1):5834.View Related Profiles. PMID: 34611166; PMCID: PMC8492657; DOI: 10.1038/s41467-021-26045-w;
     
  10. Odom CV, Kim Y, Burgess CL, Baird LA, Korkmaz FT, Na E, Shenoy AT, Arafa EI, Lam TT, Jones MR, Mizgerd JP, Traber KE, Quinton LJ. Liver-Dependent Lung Remodeling during Systemic Inflammation Shapes Responses to Secondary Infection. J Immunol. 2021 10 01; 207(7):1891-1902.View Related Profiles. PMID: 34470857; PMCID: PMC8631467; DOI: 10.4049/jimmunol.2100254;
     
Showing 10 of 53 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 53 publications over 21 distinct years, with a maximum of 6 publications in 2005 and 2017

YearPublications
20021
20031
20042
20056
20061
20072
20082
20092
20111
20124
20131
20143
20153
20161
20176
20194
20202
20213
20225
20231
20242
In addition to these self-described keywords below, a list of MeSH based concepts is available here.

cytokine
pneumonia
posttranscription
Contact for Mentoring:

72 E. Concord St Housman (R)
Boston MA 02118
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