Skip to main content

Part of UT Health San Antonio

Graduate School of Biomedical Sciences, UT Health San AntonioGraduate School of Biomedical Sciences, UT Health San Antonio

Part of UT Health San Antonio

Give
Search

Quicklinks

Commencement

  • Commencement 2021

Logins

  • Canvas
  • CourseLeaf
  • IMPACT
  • LiveMail
  • Syllabus Depot
  • My UT Health (Intranet)

Resources

  • COVID-19 Updates for Students
  • Enrolled Student Resources
  • Educational Resources
  • GSBS Data Request Form

 Close Quicklinks

 
Menu
  • About
  • Admissions
  • Programs
  • Research
  • Faculty
  • Student Life
  • Alumni

You are here

  • Faculty directory
  • Venkatachalam, Manjeri A
Venkatachalam, Manjeri A

Contact

210-567-4108

venkatachal@uthscsa.edu

Programs

M.D./Ph.D. in South Texas Medical Scientist Training Program
M.S. in Clinical Investigation & Translational Science
Ph.D. in Integrated Biomedical Sciences

Departments & Divisions

Department of Biochemistry & Structural Biology
Department of Pathology and Laboratory Medicine

Manjeri A  Venkatachalam, MBBS

Professor of Biochemistry, Professor - Pathology and Laboratory Medicine

Dr. Manjeri Venkatachalam's expertise is in acute renal failure, renal pathology, signal transduction, surgical pathology, chronic kidney disease, glomerular structure and function, molecular pathology of cell death.

RESEARCH

Mechanisms of Kidney Disease Progression 

Following acute kidney injury (AKI), renal tubules often become atrophic, giving rise to chronic kidney disease (CKD). The molecular basis for tubule atrophy after AKI is unclear. We found the mitochondrial number to be decreased and remaining mitochondria structurally defective in atrophic tubules. Our research is aimed to understand the mechanisms of mitochondrial malfunction and mitochondrial loss after AKI and develop strategies that promote tubule recovery after AKI. Our research showed that RRM2B, the alternate regulatory subunit of ribonucleotide reductase (RNR), the oxygen-dependent enzyme that produces deoxyribonucleotides (dNTPs), is severely reduced in kidney tubules regenerating after AKI. RRM2B is essential for the generation of dNTPs required for the synthesis and repair of mitochondrial DNA (mtDNA). Our hypothesis is that reactive oxygen species (ROS) produced within mitochondria in excess of basal levels damages mtDNA and impairs respiratory chain integrity. Misdirected electron transport further increases ROS production and enhances mtDNA damage. Reduced RRM2B and consequent diminished production of dNTPs impairs mtDNA synthesis and repair, compromising mitochondrial biogenesis and integrity. Because intact mitochondria are essential for cellular vitality, tubule cells recover poorly and become atrophic, secondarily giving rise to fibrosis. Ongoing experiments address the underpinnings of RRM2B regulation and investigate the critical role played by RRM2B in mtDNA synthesis and repair. We are using cell culture and in vivo transgenic approaches to decrease, delete or overexpress RRM2B as tools to arrive at the answers we seek.

Related Diseases: Acute Kidney Injury and chronic kidney disease

Techniques: Protein and RNA analysis, laser capture microdissection, CRISPR-Cas9 knockout, shRNA knockdown, Cre-Lox recombination to produce transgenic mice, Immunofluorescence and immunohistochemistry.

  • Professional Background

    Education

    • 1962 - BS - Surgery - Calcutta Medical College and Calcutta University
    • 1962 - BS - Medicine - Calcutta Medical College and Calcutta University
    • 1957 - BS - Science - St Xavier's College/Calcutta University

    Appointments

    • 9/2001 - Professor of Biochemistry - University of Texas Health Science Center, Biochemistry, San Antonio
    • 9/1979 - Professor of Medicine - University of Texas Health Science Center, Medicine, San Antonio
    • 8/1979 - Professor of Pathology - University of Texas Health Science Center, Pathology, San Antonio
  • Instruction & Training

    • - Present, Post-Doctoral Student Supervision, UTHSCSA
    • - Present, Post-Doctoral Student Supervision, UTHSCSA
    • 1/2009 - Present, Individual Instruction, University of Texas Health Science Center at San Antonio
    • 1/2000 - Present, Pathology, The University of Texas Health Science Center
  • Research & Grants

    Grants

    Federal

    Funding Agency National Institutes of Health Title Pathogenesis of Tubule Atrophy and Failed Recovery After Acute Kidney Injury Status Active Period 1/2016 - 12/2019 Role Principal Investigator Grant Detail

  • Publications

    Abstract

    Prajjal Kanti Singha, Nandita Mishra, Rekha Kar, Srilakshmi Pandeswara, Manjeri A. Venkatachalam, Pothana Saikumar. Targeting LC3-SQSTM1 (p62) signaling axis to treat apoptosis-resistant and metastatic breast cancers; 2010 Jan. (AACR). Singha PK, Pandeswara S, Venkatachalam MA, Saikumar P. TMEPAI, a Novel Prognostic Marker for TGF-β Dependency of Metastatic Breast Cancers: Converts Tumor Suppressive TGF-β into a Tumor Promoter; 2010 Jan. (SABCS Annual Meeting). Saikumar P, Mikhailov VI, Mikhailova M, Venkatachalam MA, Kar R. Bax mediated release of apoptosis inducing factors requires its dissociation from the inner mitochondrial membrane; 2004 Jan. (FASEB J; vol. 18, no. 8). Saikumar P, Mikhailov VI, Mikhailova M, Venkatachalam MA. Rapid cell death in Bcl-2 overexpressing rat proximal tubule cells exposed to cold and rewarming; 2003 Jan. (J Am Soc Nephrol; vol. 14). Saikumar P, Mikhailova M, Mikhailov VI, Venkatachalam MA, Denton ML. Caspase activation through formation of protein complexes during hypoxia or ATP depletion; 2002 Jan. (FASEB J; vol. 16, no. 4). Mikhailov VI, Mikhailova M, Venkatachalam MA, Saikumar P. Bax dependent release of apoptogenic factors from mitochondria by t-Bid; 2002 Jan. (J Am Soc Nephrol; vol. 13). Mikhailova M, Mikhailov VI, Denton ML, Dong Z, Venkatachalam MA, Saikumar P. Apoptotic protein complexes in hypoxic rat kidney proximal tubule cells; 2001 Jan. (J Am Soc Nephrol; vol. 12).

    Book Chapter

    Manjeri A Venkatachalam, Hui Geng, Rongpei Lan, Prajjal Singha, Pothana Saikumar, and Joel M Weinberg. Maladaptive Repair and AKI to CKD Transition. In: (Schnellmann, R. G. and Cummings, Brian S. Vol. Eds), McQueen, C (Chief Editor). Renal Toxicology, in Comprehensive Toxicology Third Edition, Vol. 14. New York, NY: Elsevier; 2018. p. 164-188.

    Editorial

    Venkatachalam MA
    Weinberg JM. Pericytes Preserve Capillary Integrity to Prevent Kidney Hypoxia J Am Soc Nephrol 2017 Mar;28(3):717-719. Venkatachalam MA, Weinberg JM. Fibrosis without fibroblast TGF-beta receptors? kidney international 2015 Sep;88(3):434-437. Venkatachalam MA. Could Autophagic Exhaustion Be a Final Common Pathway for Podocytopathy in FSGS? J Am Soc Nephrol 2015 May;26(5):999-1001.

    Journal Article

    Wetzel MD,
    Gao T,
    Venkatachalam M,
    Morris SM Jr,
    Awad AS. l-Homoarginine supplementation prevents diabetic kidney damage Physiological Reports 2019 Sep;7(18):2-9. Lee HJ, Gonzalez O, Dick EJ Jr, Donati A, Feliers D, Goutam Ghosh C, Ross C, Venkatachalam M, Tardif SD,Kasinath BS. Marmoset as a model to study kidney changes associated with aging J Gerontol A Biol Sci Med Sci 2019 Feb;74(3):315-324. Lan, R, Geng, H, Singha, P, Saikumar P, Bottinger, EP, Weinberg, JM, Venkatachalam MA. Mitochondrial Pathology and Glycolytic Shift during Proximal Tubule Atrophy after Ischemic AKI Journal of the American Society of Nephrology 2016 Nov;27(11):3356-3367. Kallingal GJ, Weinberg JM, Reis IM, Nehra A, Venkatachalam MA, Parekh DJ. Long-Term Response to Renal Ischemia in the Human Kidney After Partial Nephrectomy - Results from a Prospective Clinical Trial BJU Int 2016 May;117(5):766-774. Kar R, Mishra, N, Singha, PK, Venkatachalam MA, McEwen DG, Saikumar P. Mitochondrial remodeling following fission inhibition by 15d-PGJ2 involves molecular changes in mitochondrial fusion protein OPA1 Biochem. Biophys. Res. Commun 2010 Sep;399(4):548-554. Rongpei Lan, Hui Geng, Yoon Hwang, Pramod Mishra,
    Wayne L.Skloss, Eugene A. Sprague, Pothana Saikumar, and Manjeri
    A. Venkatachalam
    . A Novel Wounding Device Suitable for Quantitative Biochemical Analysis of Wound Healing and Regeneration of Cultured Epithelium Wound Repair and Regeneration 2010 Jan;18:159-167. Kar R, Mishra N, Singha P, Venkatachalam MA and Saikumar P. Mitochondrial Remodeling Following Fission Inhibition by 15d-PGJ2 Involves Molecular Changes in Mitochondrial Fusion Protein OPA1 Biochem Biophys Res Comm 2010 Jan;399(4):548-554. Mishra N, Kar R, Singha PK, Venkatachalam MA, McEwen DG, Saikumar P. Inhibition of mitochondrial division through covalent modification of Drp1 protein by 15 deoxy-Delta(12,14)-prostaglandin J2 Biochem Biophys Res Commun 2010 Jan;395(1):17-24. Kar R, Singha, PK, Venkatachalam MA, Saikumar P. A novel role of LC3 in 15-deoxy-∆12, 14 Prostaglandin J2 mediated non-autophagic cancer cell death Oncogene 2009 Jul;28(28):2556-2568. Geng, H, Lan, R, Wang, G, Siddiqi, AR, Naski MC, Brooks, AI, Barnes JL, Saikumar P, Weinberg, JM, Venkatachalam MA. Inhibition of autoregulated TGFβ signaling simultaneously enhances proliferation and differentiation of kidney epithelium and promotes repair following renal ischemia Am J Pathol 2009 Jan;174(4):1291-1308. Kar R, Singha PK, Venkatachalam MA, Saikumar P. A novel role for MAP1 LC3 in nonautophagic cytoplasmic vacuolation death of cancer cells Oncogene 2009 Jan;28(28):2556-2568. Mikhailov V, Mikhailova M, Degenhardt K, Venkatachalam MA, White E, Saikumar P. Association of Bax and Bak homo-oligomers in mitochondria. Bax requirement for Bak reorganization and cytochrome c release J Biol Chem 2003 Jan;278(7):5367-5376. Mikhailov V, Mikhailova M, Pulkrabek DJ, Dong Z, Venkatachalam MA, Saikumar P. Bcl-2 prevents Bax oligomerization in the mitochondrial outer membrane J Biol Chem 2001 Jan;276(21):18361-18374.

    Review Article

    He L Wei Q Liu Y Liu H Sun L Peng Y Liu F Venkatachalam MA Dong Z. AKI on CKD: heightened injury, suppressed repair, and the underlying mechanisms Kidney International 2017 Nov;92(5):1071-1083. Yang, Y, Song, M, Liu, Y, Liu, H, Sun, L, Peng, Y, Liu, F, Venkatachalam MA, Dong, Z. Renoprotective approaches and strategies in acute kidney injury Pharmacol Ther 2016 Jul;163:58-73. Weinberg, JM, Bienholz, A, Venkatachalam MA. The role of glycine in regulated cell death Cell Mol Life Sci pii: ASN.2015020177. [Epub ahead of print] PMID: 27000065 2016 Jun;73(11-12):2285-2308. Venkatachalam MA
    Weinberg JM
    Kriz W
    Bidani AK. Failed Tubule Recovery, AKI-CKD Transition, and Kidney Disease Progression Journal of the American Society of Nephrology 2015 Mar;26(8):1765-1776. Venkatachalam MA, Griffin KA, Lan R, Geng H, Saikumar P, Bidani AK. Acute kidney injury: a springboard for progression in chronic kidney disease Am J Physiol Renal Physiol 2010 Jan;298(5):F1078-F1094.

Map image of UT Health San Antonio location
UT Health San Antonio
Graduate School of Biomedical Sciences

7703 Floyd Curl Drive

San Antonio, TX 78229

210-567-3709

gsbs@uthscsa.edu

  • About us
  • Contact us
  • Maps & directions

We make lives better ®

The University of Texas Health Science Center at San Antonio, also called UT Health San Antonio, is a leading academic health center with a mission to make lives better through excellence in advanced academics, life-saving research and comprehensive clinical care including health, dental and cancer services.

Web Privacy | Links from websites affiliated with UT Health's website (uthscsa.edu) to other websites do not constitute or imply university endorsement of those sites, their content, or products and services associated with those sites. The content on this website is intended to be used for informational purposes only. Health information on this site is not meant to be used to diagnose or treat conditions. Consult a health care provider if you are in need of treatment.