Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin
Ever since the days of NO being proclaimed as the “molecule of the year”, the molecular effects of this miracle gas on the globins have remained elusive. While its vasodilatory role in the cardiopulmonary system and the vasculature is well recognized, the molecular underpinnings of the NO–globin axi...
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2022-09-01
|
| Series: | Cells |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4409/11/18/2838 |
| _version_ | 1827662521637535744 |
|---|---|
| author | Mamta P. Sumi Blair Tupta Arnab Ghosh |
| author_facet | Mamta P. Sumi Blair Tupta Arnab Ghosh |
| author_sort | Mamta P. Sumi |
| collection | DOAJ |
| description | Ever since the days of NO being proclaimed as the “molecule of the year”, the molecular effects of this miracle gas on the globins have remained elusive. While its vasodilatory role in the cardiopulmonary system and the vasculature is well recognized, the molecular underpinnings of the NO–globin axis are incompletely understood. We show, by transwell co-culture of nitric oxide (NO) generating, HEK eNOS/nNOS cells, and K562 erythroid or C2C12 muscle myoblasts, that low doses of NO can effectively insert heme into hemoglobin (Hb) and myoglobin (Mb), making NO not only a vasodilator, but also a globin heme trigger. We found this process to be dependent on the NO flux, occurring at low NO doses and fading at higher doses. This NO-triggered heme insertion occurred into Hb in just 30 min in K562 cells and into muscle Mb in C2C12 myoblasts between 30 min and 1 h, suggesting that the classical effect of NO on upregulation of globin (Hb or Mb) is just not transcriptional, but may involve sufficient translational events where NO can cause heme-downloading into the apo-globins (Hb/Mb). This effect of NO is unexpected and highlights its significance in maintaining globins in its heme-containing holo-form, where such heme insertions might be required in the circulating blood or in the muscle cells to perform spontaneous functions. |
| first_indexed | 2024-03-10T00:27:11Z |
| format | Article |
| id | doaj.art-f19f4aeb9f1d4cb3b801adba946e7220 |
| institution | Directory Open Access Journal |
| issn | 2073-4409 |
| language | English |
| last_indexed | 2024-03-10T00:27:11Z |
| publishDate | 2022-09-01 |
| publisher | MDPI AG |
| record_format | Article |
| series | Cells |
| spelling | doaj.art-f19f4aeb9f1d4cb3b801adba946e72202023-11-23T15:33:05ZengMDPI AGCells2073-44092022-09-011118283810.3390/cells11182838Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle MyoglobinMamta P. Sumi0Blair Tupta1Arnab Ghosh2Department of Inflammation and Immunity, Lerner Research Institute, The Cleveland Clinic, Cleveland, OH 44195, USADepartment of Inflammation and Immunity, Lerner Research Institute, The Cleveland Clinic, Cleveland, OH 44195, USADepartment of Inflammation and Immunity, Lerner Research Institute, The Cleveland Clinic, Cleveland, OH 44195, USAEver since the days of NO being proclaimed as the “molecule of the year”, the molecular effects of this miracle gas on the globins have remained elusive. While its vasodilatory role in the cardiopulmonary system and the vasculature is well recognized, the molecular underpinnings of the NO–globin axis are incompletely understood. We show, by transwell co-culture of nitric oxide (NO) generating, HEK eNOS/nNOS cells, and K562 erythroid or C2C12 muscle myoblasts, that low doses of NO can effectively insert heme into hemoglobin (Hb) and myoglobin (Mb), making NO not only a vasodilator, but also a globin heme trigger. We found this process to be dependent on the NO flux, occurring at low NO doses and fading at higher doses. This NO-triggered heme insertion occurred into Hb in just 30 min in K562 cells and into muscle Mb in C2C12 myoblasts between 30 min and 1 h, suggesting that the classical effect of NO on upregulation of globin (Hb or Mb) is just not transcriptional, but may involve sufficient translational events where NO can cause heme-downloading into the apo-globins (Hb/Mb). This effect of NO is unexpected and highlights its significance in maintaining globins in its heme-containing holo-form, where such heme insertions might be required in the circulating blood or in the muscle cells to perform spontaneous functions.https://www.mdpi.com/2073-4409/11/18/2838apo-globinshemeheme insertionmyoblastsnitric oxide |
| spellingShingle | Mamta P. Sumi Blair Tupta Arnab Ghosh Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin Cells apo-globins heme heme insertion myoblasts nitric oxide |
| title | Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin |
| title_full | Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin |
| title_fullStr | Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin |
| title_full_unstemmed | Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin |
| title_short | Nitric Oxide Trickle Drives Heme into Hemoglobin and Muscle Myoglobin |
| title_sort | nitric oxide trickle drives heme into hemoglobin and muscle myoglobin |
| topic | apo-globins heme heme insertion myoblasts nitric oxide |
| url | https://www.mdpi.com/2073-4409/11/18/2838 |
| work_keys_str_mv | AT mamtapsumi nitricoxidetrickledriveshemeintohemoglobinandmusclemyoglobin AT blairtupta nitricoxidetrickledriveshemeintohemoglobinandmusclemyoglobin AT arnabghosh nitricoxidetrickledriveshemeintohemoglobinandmusclemyoglobin |