Matthew R. Hodges, PhD, FAPS
Professor and Eminent Scholar; Director of Graduate Studies
Locations
- Physiology
Contact Information
Education
PhD, Physiology, Medical College of Wisconsin, 2004
BA, Biology, Carleton College, 1998
Methodologies and Techniques
- Blotting, Western
- Breathing measurements in small and large mammals
- Electrophysiology
- Immunohistochemistry
- Microdialysis
- Microscopy
- Microscopy, Fluorescence
- Plethysmography, Whole Body
- Polymerase Chain Reaction
- RNA Sequencing (transcriptomics)
Leadership Positions
- Director NIH Predoctoral T32 Training Grant in Physiology
- Director of Graduate Studies, Physiology
Research Interests
Genetics and Genomics | Neurophysiology | Respiratory Physiology
Every cell in the body requires a continuous supply of oxygen and constant removal of carbon dioxide, and as a result we breathe continuously from birth to death to ensure adequate gas exchange. A decrease in the blood oxygen levels or an increase in carbon dioxide (which decreases pH) both acting to increase ventilation in classic feedback fashion. However, it remains unknown which neurons within the brainstem serve as detectors of brain carbon dioxide (CO2) levels and/or pH, and how these neurons send this information to the neuronal network that generate respiratory rhythm and muscle activation patterns.
We are currently using fluorescence-activated cell sorting (FACS) of primary neurons to collect CO2-activated serotonergic (5-HT) and glutamatergic (RTN) neurons and compare them to cells that are not activated by high CO2 and/or low pH. We extract mRNAs from these cell pools and identify and measure the expression levels of all genes in order to determine which genes are uniquely expressed in the CO2-sensitive populations. These gene targets are then manipulated in vitro (neuronal recordings and pharmacologic agents) or in vivo (knockout or mutant rat strains) to verify their potential role in breathing control and pH homeostasis. This project is funded by the NIH.
Sudden Infant Death Syndrome (SIDS) is a leading cause of post-neonatal mortality in the U.S. and the Western World. SIDS is a devastating disease, and one that is difficult to understand. Recent research has identified abnormalities in the brainstem serotonin (5-HT) system in SIDS cases, suggesting the neurons that make 5-HT could contribute to the sudden and unexpected death. In the Hodges Lab, we study the effects of brain depletion of tryptophan hydroxylase, and as a result brain depletion of 5-HT. We study how these abnormalities, which are found in SIDS, affect physiological systems necessary for sustaining life, like breathing and body temperature control, and how additional environmental (increased heat) and other (inflammation) stressors affect these systems. This project is a collaboration with the PI (Hodges) and Drs. Cummings (University of Missouri) and Huxtable (University of Oregon), and was previously funded by the NIH and Children’s Research Institute at Children's Wisconsin (additional funding pending).
We are also currently studying the role of a potassium ion channel subunit gene (Kcnj16) and how it contributes to the acute and chronic regulation of body pH. We are gaining major insights into the role of Kcnj16 in the control of breathing and the CO2 chemoreflex by studying rats with a truncation mutation in the coding region of the gene. These rats may be important rodent models for the epilepsy and potentially Sudden Unexplained Death in Epilepsy (SUDEP). This project is collaboration with the PI (Hodges) and Dr. Oleg Palygin (Physiology). This project is funded by the Advancing Healthier Wisconsin Foundation and Neuroscience Research Center at MCW.
A fourth project ongoing in the lab is the study of changes in ventilatory control associated with neonatal lung dysfunction, using a rodent model of bronchopulmonary dysplasia. While the lungs are the primary cause of ventilatory distress in babies with pulmonary disease, ultimately the neural network that controls breathing that adapts to this abnormality and adapts. The extent of this neural adaptation, or neuroplasticity is unclear, but has become another focus of research in the lab. This project is a collaboration with the PI (Hodges) and two additional MCW faculty, Drs. Konduri (Section Chief, Neonatology) and Wong-Riley (Professor, Cell Biology, Neurobiology and Anatomy), and is funded by the Children's Research Institute at Children's Wisconsin.
Mentorship
In addition to training eight (8) undergraduate and two (2) medical students in the Hodges Lab, graduate students from the Physiology Doctoral Program and Neuroscience Doctoral Programs have obtained their PhD in the lab, including:
Gary C. Mouradian, Jr., PhD
Currently a Post-doctoral Fellow at the University of Colorado-Denver, Anschutz Medical Campus, Denver, CO
Madeleine M. Puissant, PhD
Currently an EMS Faculty and Clinical Coordinator, Northcentral Technical College, Wausau, WI
Publications
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(Wan T, Rousseau H, Mattern C, Tabor M, Hodges MR, Ramchandran R, Spearman AD.) bioRxiv. 2024 Apr 05 PMID: 38617317 PMCID: PMC11014550 04/15/2024
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(Osmani WA, Gallo A, Tabor M, Eilbes M, Cook-Snyder DR, Hodges MR.) Front Physiol. 2024;15:1413479 PMID: 39175614 PMCID: PMC11339535 SCOPUS ID: 2-s2.0-85201577675 08/23/2024
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Do peripheral and central sites independently contribute to the CO2 stimulus for breathing?
(Forster HV, Hodges MR.) J Physiol. 2024 Jan;602(1):9-10 PMID: 38103001 SCOPUS ID: 2-s2.0-85179960112 12/16/2023
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(Grams KJ, Neumueller SE, Mouradian GC Jr, Burgraff NJ, Hodges MR, Pan L, Forster HV.) Physiol Genomics. 2023 Nov 01;55(11):487-503 PMID: 37602394 PMCID: PMC11178267 SCOPUS ID: 2-s2.0-85173579485 08/21/2023
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Repeated seizures lead to progressive ventilatory dysfunction in SSKcnj16-/- rats.
(Manis AD, Cook-Snyder DR, Duffy E, Osmani WA, Eilbes M, Dillard M, Palygin O, Staruschenko A, Hodges MR.) J Appl Physiol (1985). 2023 Oct 01;135(4):872-885 PMID: 37535709 PMCID: PMC10642517 SCOPUS ID: 2-s2.0-85174642163 08/03/2023
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(Balapattabi K, Yavuz Y, Jiang J, Deng G, Mathieu NM, Ritter ML, Opichka MA, Reho JJ, McCorvy JD, Nakagawa P, Morselli LL, Mouradian GC Jr, Atasoy D, Cui H, Hodges MR, Sigmund CD, Grobe JL.) Cell Rep. 2023 Aug 29;42(8):112935 PMID: 37540598 PMCID: PMC10530419 SCOPUS ID: 2-s2.0-85169503465 08/04/2023
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(Neumueller SE, Buiter N, Hilbert G, Grams K, Taylor R, Desalvo J, Hodges GL, Hodges MM, Pan LG, Lewis SJ, Forster HV, Hodges MR.) Front Physiol. 2023;14:1277601 PMID: 37885800 PMCID: PMC10598602 SCOPUS ID: 2-s2.0-85174973708 10/27/2023
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(Mathieu NM, Fekete EM, Muskus PC, Brozoski DT, Lu KT, Wackman KK, Gomez J, Fang S, Reho JJ, Grobe CC, Vazirabad I, Mouradian GC Jr, Hodges MR, Segar JL, Grobe JL, Sigmund CD, Nakagawa P.) Function (Oxf). 2023;4(5):zqad043 PMID: 37609445 PMCID: PMC10440998 SCOPUS ID: 2-s2.0-85168790693 08/23/2023
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HomeCageScan analysis reveals ongoing pain in Fabry rats.
(Burand AJ Jr, Waltz TB, Manis AD, Hodges MR, Stucky CL.) Neurobiol Pain. 2023;13:100113 PMID: 36660199 PMCID: PMC9843259 01/21/2023
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(Buchholz KJ, Neumueller SE, Burgraff NJ, Hodges MR, Pan L, Forster HV.) J Appl Physiol (1985). 2022 Nov 01;133(5):1106-1118 PMID: 36135953 PMCID: PMC9621709 SCOPUS ID: 2-s2.0-85141003919 09/23/2022
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Kir5.1 channels: potential role in epilepsy and seizure disorders.
(Staruschenko A, Hodges MR, Palygin O.) Am J Physiol Cell Physiol. 2022 Sep 01;323(3):C706-C717 PMID: 35848616 PMCID: PMC9448276 SCOPUS ID: 2-s2.0-85137124646 07/19/2022
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(Mouradian GC Jr, Liu P, Nakagawa P, Duffy E, Gomez Vargas J, Balapattabi K, Grobe JL, Sigmund CD, Hodges MR.) Front Synaptic Neurosci. 2022;14:910820 PMID: 35844900 PMCID: PMC9280690 SCOPUS ID: 2-s2.0-85134237459 07/19/2022